Yoshito Kishi
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Japanese Professor of Chemistry
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Chemistry
Yoshito Kishi's Degrees
- Bachelors Chemistry Kyoto University
Why Is Yoshito Kishi Influential?
(Suggest an Edit or Addition)According to Wikipedia, was a Japanese chemist who was the Morris Loeb Professor of Chemistry at Harvard University. He was known for his contributions to the sciences of organic synthesis and total synthesis. Early life and education Kishi was born in Nagoya, Japan and attended Nagoya University, where he obtained both his BS and PhD degrees. He was a postdoctoral research fellow at Harvard University where he worked with Robert Burns Woodward. From 1966 through 1974, he was a professor of chemistry at Nagoya University. Since 1974, Kishi had been a professor of chemistry at Harvard University.
Yoshito Kishi's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosides (1982) (467)
- In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B. (2001) (442)
- Catalytic effect of nickel(II) chloride and palladium(II) acetate on chromium(II)-mediated coupling reaction of iodo olefins with aldehydes (1986) (374)
- On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical rule (1983) (347)
- Total synthesis of halichondrin B and norhalichondrin B (1992) (297)
- Further synthetic studies on rifamycin s (1981) (273)
- Induction of Morphological and Biochemical Apoptosis following Prolonged Mitotic Blockage by Halichondrin B Macrocyclic Ketone Analog E7389 (2004) (228)
- Dramatic rate enhancement of Suzuki diene synthesis: its application to palytoxin synthesis (1987) (207)
- Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonide (1982) (178)
- Semi-synthetic aequorins with improved sensitivity to Ca2+ ions. (1989) (163)
- Reductive ring openings of allyl-alcohol epoxides (1982) (156)
- A total synthesis of lasalocid A (1978) (149)
- Synthesis of mono- and unsymmetrical bis-orthoesters of scyllo-inositol (1985) (138)
- Light-emitting properties of recombinant semi-synthetic aequorins and recombinant fluorescein-conjugated aequorin for measuring cellular calcium. (1993) (135)
- A stereospecific total synthesis of d,l-saxitoxin. (1977) (125)
- Eribulin induces irreversible mitotic blockade: implications of cell-based pharmacodynamics for in vivo efficacy under intermittent dosing conditions. (2011) (123)
- Macrocyclic ketone analogues of halichondrin B. (2004) (122)
- Synthetic studies on tetrodotoxin and related compounds. IV. Stereospecific total syntheses of DL-tetrodotoxin. (1972) (119)
- An improved procedure for the Blaise reaction: a short, practical route to the key intermediates of the saxitoxin synthesis (1983) (119)
- Synthetic studies on polyether antibiotics. 5. Total synthesis of monensin. 2. Stereocontrolled synthesis of the right half of monensin (1979) (117)
- Recombinant aequorin and recombinant semi-synthetic aequorins. Cellular Ca2+ ion indicators. (1990) (115)
- Complete Relative Stereochemistry of Maitotoxin (1996) (112)
- Semi-synthetic aequorin. An improved tool for the measurement of calcium ion concentration. (1988) (110)
- Structure of dinoflagellate luciferin and its enzymic and nonenzymic air-oxidation products (1989) (110)
- Stereochemistry of palytoxin. 4. Complete structure (1982) (106)
- Total synthesis of a fully protected palytoxin carboxylic acid (1989) (104)
- Total Synthesis of Altohyrtin A (Spongistatin 1): Part 1 (1998) (103)
- Synthetic studies on tetrodotoxin and related compounds. 3. A stereospecific synthesis of an equivalent of acetylated tetrodamine. (1972) (102)
- Structural basis of protein kinase C activation by tumor promoters. (1989) (99)
- On stereochemistry of osmium tetroxide oxidation of allylic alcohol systems: examples (1983) (95)
- Practical asymmetric synthesis of aklavinone (1982) (94)
- Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building block (1980) (94)
- Total synthesis of (+)-ophiobolin C (1989) (92)
- Synthesis of Palytoxin from Palytoxin Carboxylic Acid (1994) (90)
- A total synthesis of sporidesmin A. (1973) (86)
- Operationally simple and efficient workup procedure for TBAF-mediated desilylation: application to halichondrin synthesis. (2007) (86)
- A mild preparation of vinyliodides from vinylsilanes (1996) (84)
- Ni(II)/Cr(II)-mediated coupling reaction: an asymmetric process (1995) (81)
- Toward Creation of a Universal NMR Database for Stereochemical Assignment: The Case of 1,3,5-Trisubstituted Acyclic Systems (2000) (79)
- Toolbox approach to the search for effective ligands for catalytic asymmetric Cr-mediated coupling reactions. (2009) (78)
- Complete structure of the mycolactones. (2001) (78)
- The relative rate of aequorin regeneration from apoaequorin and coelenterazine analogues. (1993) (76)
- Total synthesis of gliotoxin, dehydrogliotoxin and hyalodendrin (1981) (75)
- Asymmetric Ni(II)/Cr(II)-mediated coupling reaction: catalytic process. (2002) (75)
- Fe/Cr- and Co/Cr-mediated catalytic asymmetric 2-haloallylations of aldehydes. (2004) (71)
- Letter: Synthetic studies on histrionicotoxins. I. A stereocontrolled synthesis of (plus or minus)-perhydrohistrionicotoxin. (1975) (71)
- TOTAL SYNTHESIS OF ALTOHYRTIN A (SPONGISTATIN 1) : PART 2 (1998) (71)
- Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: the case of two contiguous propionate units. (1999) (69)
- Universal NMR databases for contiguous polyols. (2003) (67)
- Synthesis of C-disaccharides (1987) (67)
- Stereochemistry of the core structure of the mycolactones. (2001) (66)
- Practical total synthesis of (.+-.)-aklavinone and total synthesis of aklavin (1981) (66)
- Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products. (2001) (65)
- Aldol reaction of allenolates generated via 1,4-addition of iodide anion or its equivalent to α,β-acetylenic ketones (1986) (65)
- SYNTHETIC STUDIES ON POLYETHER ANTIBIOTICS. 6. TOTAL SYNTHESIS OF MONENSIN. 3. STEREOCONTROLLED TOTAL SYNTHESIS OF MONENSIN (2002) (64)
- Synthetic studies towards halichondrins (1987) (64)
- Stereospecific total synthesis of dl-austamide (1979) (63)
- New method for the synthesis of epidithiodiketopiperazines (1973) (61)
- Preferred conformation of C-glycosides. 8. Synthesis of 1,4-linked carbon disaccharides (1992) (61)
- Total synthesis of onnamide A (1991) (61)
- Chemistry of mycolactones, the causative toxins of Buruli ulcer (2011) (61)
- A total synthesis of gliotoxin. (1976) (60)
- New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: double-inversion approach. (2009) (60)
- Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural products (1980) (60)
- Applications of Ni(II)/Cr(II)-mediated coupling reactions to natural products syntheses (1992) (59)
- Total synthesis of (.+-.)-gephyrotoxin (1980) (59)
- Structural basis of protein kinase C activation by diacylglycerols and tumor promoters. (1992) (59)
- New catalytic cycle for couplings of aldehydes with organochromium reagents. (2004) (58)
- Asymmetric Ni(II)/Cr(II)-mediated coupling reaction: stoichiometric process. (2002) (58)
- New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: reductive cyclization and oxy-Michael cyclization approaches. (2009) (57)
- Structurally simplified macrolactone analogues of halichondrin B. (2004) (57)
- Biological Evaluation of Rationally Modified Analogs of the H-Type II Blood Group Trisaccharide. A Correlation between Solution Conformation and Binding Affinity (1995) (57)
- Preferred conformation of C-glycosides. 6. Conformational similarity of glycosides and corresponding C-glycosides (1987) (56)
- Preferred Conformation of C-Lactose at the Free and Peanut Lectin Bound States (1998) (56)
- Total synthesis of rifamycins. 2. Total synthesis of racemic rifamycin S (1980) (56)
- Dramatic improvement in catalyst loadings and molar ratios of coupling partners for Ni/Cr-mediated coupling reactions: heterobimetallic catalysts. (2009) (55)
- Synthetic studies on polyether antibiotics. II. Stereocontrolled syntheses of epoxides of bishomoallylic alcohols. (1978) (55)
- Total synthesis of the mycolactones. (2002) (55)
- Experimental Support for the Primary Stereoelectronic Effect Governing Baeyer−Villiger Oxidation and Criegee Rearrangement (1998) (54)
- The Total Synthesis of Mitomycins (1979) (53)
- Total Synthesis of (±)-Batrachotoxinin A (1998) (53)
- Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols. (2002) (53)
- On the absolute configuration of gephyrotoxin (1982) (52)
- Synthesis and structure of tolyporphin A O,O-diacetate. (1999) (52)
- Preferred conformation of C-glycosides. 10. Synthesis and conformational analysis of carbon trisaccharides (1992) (52)
- Total synthesis of debromoaplysiatoxin and aplysiatoxin (1987) (51)
- Synthetic studies toward mitomycins. 2. Total synthesis of dl-porfiromycin (1977) (51)
- Letter: Synthetic studies on histrionicotoxins. II. A practical synthetic route to (plus or minus)-perhydro-and (plus or minus)-octahydrohistrionicotoxin. (1975) (50)
- A total synthesis of dehydrogliotoxin. (1973) (50)
- Cypridina bioluminescence III total synthesis of luciferin (1966) (50)
- Enantioselective total synthesis of (-)-decarbamoylsaxitoxin (1992) (50)
- Structure of the light emitter in krill (Euphausia pacifica) bioluminescence (1988) (49)
- Discovery of E7389, a Fully Synthetic Macrocyclic Ketone Analog of Halichondrin B (2005) (48)
- Stereochemistry of palytoxin. Part 1. C85-C115 segment (1982) (48)
- Synthetic studies on ophiobolins (1988) (48)
- Preferred Conformations of C-Glycosides. 14. Synthesis and Conformational Analysis of Carbon Analogs of the Blood Group Determinant H-Type II (1995) (48)
- Synthetic studies toward mitomycins. 1. Total synthesis of deiminomitomycin A. (1977) (48)
- Unified total synthesis of pteriatoxins and their diastereomers. (2006) (48)
- Total synthesis of halichondrin C. (2012) (47)
- Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: proof of concept. (1999) (46)
- β-Halovinyl ketones: Synthesis from acetylenic ketones (1986) (46)
- New Synthetic Route to the C.14−C.38 Segment of Halichondrins (1997) (46)
- Total synthesis of mycalamides A and B (1990) (46)
- Structure-activity relationships of halichondrin B analogues: modifications at C.30-C.38. (2000) (45)
- Luciferins, bioluminescent substances. (1968) (45)
- Preferred conformation of C-glycosides. 12. Synthesis and conformational analysis of .alpha.,.alpha.-, .alpha.,.beta.-, and .beta.,.beta.-C-trehaloses (1994) (45)
- Catalytic enantioselective Cr-mediated propargylation: application to halichondrin synthesis. (2009) (45)
- Practical asymmetric syntheses of 11-deoxydaunomycinone and related compounds (1982) (45)
- Total synthesis of rifamycin S (1981) (45)
- Application of chiral lanthanide shift reagents for assignment of absolute configuration of alcohols. (2004) (44)
- Preferred conformation of C-glycosides. 9. Conformational analysis of 1,4-linked carbon disaccharides (1992) (44)
- New epoxidation with m-chloroperbenzoic acid at elevated temperatures (1972) (44)
- Surprisingly efficient catalytic Cr-mediated coupling reactions. (2005) (43)
- Cooperative effect by a hydroxy and ether oxygen in epoxidation with a peracid (1980) (43)
- Complete structure of maitotoxin (1998) (42)
- Synthetiic studies toward mitomycins. III. Total syntheses of mitomycins A and C (1977) (42)
- Synthetic Studies towards Halichondrins: Synthesis of the C.27–C.38 Segment (1992) (42)
- Preferred conformation of C-glycosides. 7. Preferred conformation of carbon analogs of isomaltose and gentiobiose (1991) (42)
- Preferred conformation of C-glycosides. 2. Preferred conformation of carbon analogs of isomaltose and gentiobiose (1987) (41)
- Natural products synthesis: palytoxin (1989) (41)
- Novel Structure Elucidation of AAL Toxin TA Backbone (1994) (41)
- Stereochemistry of palytoxin. Part 2. C1-C6, C47-C74, and C77-C83 segments (1982) (41)
- The structure confirmation of the light-emitting moiety of bioluminescent jellyfish (1972) (40)
- Biomimetic macrocycle-forming Diels-Alder reaction of an iminium dienophile: synthetic studies directed toward gymnodimine. (2005) (40)
- The Stereochemical Assignment and Conformational Analysis of the V/W-Ring Juncture of Maitotoxin (1997) (40)
- Further studies on chromium(II)-mediated homoallylic alcohol syntheses (1982) (39)
- Broad spectrum preclinical antitumor activity of eribulin (Halaven(R)): optimal effectiveness under intermittent dosing conditions. (2012) (39)
- Total Synthesis of the Proposed Structure of (+)-Tolyporphin A O,O-Diacetate. (1999) (38)
- Catalytic Ni/Cr-mediated macrocyclization without use of high-dilution techniques. (2005) (37)
- A total synthesis of polyether antibiotic (−)-A23187 (calcimycin) (1987) (36)
- Revised Structure of Tolyporphin A. (1999) (36)
- Highly sensitive, operationally simple, cost/time effective detection of the mycolactones from the human pathogen Mycobacterium ulcerans. (2010) (36)
- A total synthesis of d,1-histrionicotoxin (1985) (36)
- Preferred conformation of C-glycosides. 3. Preferred conformation of carbon analogs of 1,4-disaccharides (1987) (36)
- Total synthesis of halichondrin A, the missing member in the halichondrin class of natural products. (2014) (36)
- Stereochemistry of palytoxin. Part 3. C7-C51 segment (1982) (36)
- Synthetic studies on palytoxin. Stereocontrolled, practical synthesis of the C.101-C.115 segment (1983) (36)
- Letter: Biogenetic-type synthesis of penicillin-cephalosporin antibiotics. I. A stereocontrolled synthesis of the penam- and cephem-ring systems from an acyclic tripeptide equivalent. (1975) (35)
- A new method for translating the asymmetric Ni/Cr-mediated coupling reactions from stoichiometric to catalytic. (2005) (35)
- Consequences of Interaction of a Lipophilic Endotoxin Antagonist with Plasma Lipoproteins (2000) (35)
- Enantioselective Total Synthesis of Fumonisin B2 (1997) (35)
- Further improvement on sulfonamide-based ligand for catalytic asymmetric 2-haloallylation and allylation. (2008) (34)
- Accelerated Detection of Mycolactone Production and Response to Antibiotic Treatment in a Mouse Model of Mycobacterium ulcerans Disease (2014) (34)
- Synthetic studies on halichondrins: A new practical synthesis of the C.1–C.12 segment (1993) (33)
- Structure determination of mycolactone C via total synthesis. (2004) (33)
- Complete stereochemistry of tetrafibricin. (2003) (33)
- Ni(II)/Cr(II)-Mediated Coupling Reaction: Beneficial Effects of 4-tert-Butylpyridine as an Additive and Development of New and Improved Workup Procedures (1997) (32)
- Attempts to assemble a universal NMR database without synthesis of NMR database compounds. (2006) (32)
- Stereochemistry of pteriatoxins A, B, and C. (2006) (32)
- Total synthesis and stereochemistry of mycolactone F. (2008) (32)
- A synthesis of the aromatic segment of rifamycin s (1981) (32)
- Further studies on stereospecific epoxidation of allylic alcohols Iltifat Hasan (1980) (32)
- Preferred Conformation of C-Glycosides. 13. A Comparison of the Conformational Behavior of Several C-, N-, and O-Furanosides (1994) (31)
- Synthetic studies toward the taxane class of natural products (1993) (31)
- Chiral analogs of enterobactin with hydrophilic or lipophilic properties (1993) (30)
- Synthesis of C-sucrose (1988) (30)
- Case History: Discovery of Eribulin (HALAVEN™), a Halichondrin B Analogue That Prolongs Overall Survival in Patients with Metastatic Breast Cancer (2011) (29)
- Synthesis of DNA Oligomers Possessing a Covalently Cross-Linked Watson-Crick Base Pair Model. (2001) (29)
- Suppression of Murine Endotoxin Response by E5531, a Novel Synthetic Lipid A Antagonist (1998) (29)
- Extension of the Eschenmoser sulfide contraction/iminoester cyclization method to the synthesis of tolyporphin chromophore (1997) (28)
- REACTION OF METHYLCERIUM REAGENT WITH TERTIARY AMIDES : SYNTHESIS OF SATURATED AND UNSATURATED KETONES FROM TERTIARY AMIDES (1998) (28)
- Synthetic studies towards batrachotoxin 1. A furan-based intramolecular diels-alder route to construct the a-d ring system (1994) (28)
- Palytoxin: an inexhaustible source of inspiration—personal perspective (2002) (28)
- Preferred conformation of C-glycosides. 4. Importance of 1,3-diaxial-like interactions around the nonglycosidic bond: prediction and experimental proof (1988) (27)
- Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction. (2000) (27)
- Letter: Biogenetic-type synthesis of penicillin-cephalosporin antibiotics. II. An oxidative cyclization route to beta-lactam thiazoline derivatives. (1975) (27)
- Total Synthesis of Mycolactones A and B. (2007) (27)
- A simple but remarkably effective device for forming the C8-C14 polycyclic ring system of halichondrin B. (2004) (27)
- Chlorophyll Catabolism Leading to the Skeleton of Dinoflagellate and Krill Luciferins: Hypothesis and Model Studies. (2001) (27)
- Structure of the functional part of photoprotein aequorin (1986) (27)
- β-selective C-glycosidations: lewis-acid mediated reactions of carbohydrates with silyl ketene acetals (1997) (26)
- A practical synthesis of trans-iodoolefins (1986) (26)
- Iterative Cr-mediated catalytic asymmetric allylation to synthesize syn/syn- and anti/anti-1,3,5-triols. (2008) (26)
- Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement. (2009) (26)
- Zirconium/Nickel-Mediated One-Pot Ketone Synthesis. (2017) (26)
- Structure of Dinoflagellate Luciferin and Its Enzymatic and Nonenzymatic Air-Oxidation Products (1990) (26)
- Total Synthesis of d,l-Saxitoxin (1980) (26)
- Relative and absolute stereochemistry of the fumonisin B2 backbone (1994) (26)
- Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept. (2001) (25)
- Validation of lanthanide chiral shift reagents for determination of absolute configuration: total synthesis of glisoprenin A. (2004) (25)
- STEREOCHEMISTRY OF PALYTOXIN (1983) (25)
- Preferred solution conformation of marine natural product palytoxin and of C-glycosides and their parent glycosides (1993) (25)
- Stereochemistry of sagittamide A: prediction and confirmation. (2006) (25)
- On Ni catalysts for catalytic, asymmetric Ni/Cr-mediated coupling reactions. (2012) (25)
- Synthetic approach towards tetrodotoxin. II. A stereospecific synthesis of a compound having the same six chiral centers on the cyclohexane ring as those of tetrodotoxin. (1970) (25)
- Synthetic approach towards tetrodotoxin. I. Diels-Alder reaction of α-oximinoethylbenzoquinones with butadiene (1970) (24)
- Conformationally Rigid Tricyclic Tripods: Synthesis and Application to Preparation of Enterobactin Analogs (1994) (24)
- Synthesis and structure of mycolactone E isolated from frog mycobacterium. (2008) (24)
- Second generation synthesis of C27-C35 building block of E7389, a synthetic halichondrin analogue. (2009) (24)
- Luciferin and luciopterin isolated from the Japanese firefly, Luciola cruciata. (1968) (23)
- Synthetic studies on polyether antibiotics. III. A stereocontrolled synthesis of isolasalocid ketone from acyclic precursors. (1978) (23)
- Investigations of the intramolecular Ni(II)/Cr(II)-mediated coupling reaction: Application to the taxane ring system (1993) (23)
- The structure op tetrodotoxin (1963) (23)
- HIGHLY STEREOSELECTIVE APPROACHES TO α- AND β-C-GLYCOPYRANOSIDES (1982) (22)
- Total synthesis and stereochemistry of pinnatoxins B and C. (2006) (22)
- Efficacy of Rifampin Plus Clofazimine in a Murine Model of Mycobacterium ulcerans Disease (2015) (22)
- Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds. (2001) (22)
- Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation. (2001) (22)
- Covalently Cross-Linked Watson-Crick Base Pair Models. (1999) (22)
- Simple, Rapid Mycobacterium ulcerans Disease Diagnosis from Clinical Samples by Fluorescence of Mycolactone on Thin Layer Chromatography (2015) (21)
- Synthetic 3-O-methylmannose-containing polysaccharides (sMMPs): design and synthesis. (2007) (21)
- Scalable and efficient synthesis of the mycolactone core. (2010) (21)
- Synthetic Studies Towards Halichondrins: Synthesis of the Left Half of Halichondrins (1992) (21)
- A Novel Example for Optical Resolution of Racemic Ketones Originating from Batrachotoxin Synthesis. (1998) (21)
- Cypridina bioluminescence II structural studies of luciferin by means of a high resolution mass spectrometer and an amino acid analyzer (1966) (21)
- Unified, Efficient, and Scalable Synthesis of Halichondrins: Zirconium/Nickel-Mediated One-Pot Ketone Synthesis as the Final Coupling Reaction. (2017) (21)
- One-Pot Ketone Synthesis with Alkylzinc Halides Prepared from Alkyl Halides via a Single Electron Transfer (SET) Process: New Extension of Fukuyama Ketone Synthesis. (2016) (21)
- Cypridina bioluminescence—VII : The bioluminescence of Cypridina luciferin analogs (1973) (21)
- Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: scope and limitation (2003) (21)
- Structure and synthesis of leonurine (1969) (20)
- Assignment of the relative and absolute configurations of acyclic secondary 1,2-diols (2004) (20)
- STEREOCHEMISTRY OF PALYTOXIN. PART 4. COMPLETE STRUCTURE (1983) (19)
- Preferred conformation of C-glycosides. 11. C-Sucrose: new practical synthesis, structural reassignment, and solid-state and solution conformation of its octaacetate (1993) (19)
- Use of a chiral praseodymium shift reagent in predicting the complete stereostructure of glisoprenin A. (2004) (19)
- A TOTAL SYNTHESIS OF D,L-SPORIDESMIN B (1974) (19)
- Synthetic studies towards halichondrins synthesis of the left halves of norhalichondrins and homohalichondrins (1992) (18)
- Absolute configuration at the tricarballylic acid moieties of fumonisin B1 and AAL toxin TA (1995) (18)
- Aspects of the Mechanism of Bioluminescence (1973) (18)
- [Synthetic studies on echinulin and related natural products. V. Isolation, structure and synthesis of echinulin-neoechinulin type alkaloids isolated from Aspergillus amstelodami (author's transl)]. (1977) (18)
- A landmark in drug discovery based on complex natural product synthesis (2019) (18)
- Synthetic study on echinulin and related compounds. Part I. acid-catalyzed amino claisen rearrangement of allyl- and 3,3-dimethylallyl-aniline derivatives (1971) (18)
- The pharmacophore of debromoaplysiatoxin responsible for protein kinase C activation. (1991) (18)
- Anti-endotoxin activity of a novel synthetic lipid A analog. (1995) (17)
- Highly stereoselective and iterative synthesis of alpha-(1-->4)-linked polysaccharides composed of 3-O-methyl-D-mannose. (2007) (17)
- Structure and non-enzymatic light emission of two luciferin precursors isolated from the luminous mushroom Panellus stipticus. (1993) (17)
- Extension of the Criegee Rearrangement: Synthesis of Enol Ethers from Secondary Allylic Hydroperoxides (1994) (17)
- Preferred conformation of C-glycosides. 5. Experimental support for the conformational similarity between C- and O-disaccharides (1988) (17)
- Synthetic studies towards batrachotoxin 2. Formation of the oxazepane ring system via a Michael reaction (1994) (17)
- Air-stable heterobimetallic catalysts to effect Ni/Cr-mediated couplings with a ca. 1:1 molar ratio of coupling partners at low catalyst loadings. (2012) (17)
- Absolute configuration at the tricarballylic acid moieties of fumonisin B2 (1995) (17)
- Selective activation/coupling of polyhalogenated nucleophiles in ni/cr-mediated reactions: synthesis of c1-c19 building block of halichondrin bs. (2015) (16)
- Synthetic 6-O-methylglucose-containing polysaccharides (sMGPs): design and synthesis. (2007) (16)
- Total Synthesis and Stereochemistry of Cytoblastin (1996) (16)
- Synthesis and structure assignment of the minor metabolite arising from the frog pathogen Mycobacterium liflandii. (2010) (16)
- Total Synthesis of Halichondrin B and Norhalichondrin B. (1992) (16)
- Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Proof. (2000) (16)
- [Synthesis of Cypridina luciferin and related compounds. I. Synthesis of 2-amino-5-(3-indolyl)-pyrazine]. (1969) (16)
- Effective Procedure for Selective Ammonolysis of Monosubstituted Oxiranes: Application to E7389 Synthesis. (2007) (15)
- A promising cyclization reaction to construct the saxitoxin ring system (1977) (15)
- Fe/Cu-Mediated One-Pot Ketone Synthesis. (2017) (15)
- Terminal epoxidation of farnesate attached to helical peptides. (1986) (14)
- A new, efficient synthesis of the left half of narasin (1987) (14)
- [Synthesis of Cypridina luciferin and related compounds. 3. Synthesis of cypridina luciferin]. (1969) (14)
- New conditions for controlled Claisen rearrangements of allyl aryl ethers (1976) (14)
- Concise and highly stereoselective synthesis of the C20-C26 building block of halichondrins and Eribulin. (2012) (14)
- Covalently cross-linked Watson-Crick base pair models. Part 2 (2000) (13)
- Mycobacterium ulcerans causes minimal pathogenesis and colonization in medaka (Oryzias latipes): an experimental fish model of disease transmission. (2012) (13)
- Cypridina bioluminescence—IX: Tautomeric structures of 2-methyl-3,7-dihydroimidazo[1,2-a]-pyrazin-3-one, 2-methyl-3-aminoimidazo[1,2-a]pyrazine and their derivatives in neutral and acidic media (1975) (13)
- Heterogeneity in the stereochemistry of mycolactones isolated from M. marinum: toxins produced by fresh vs. saltwater fish pathogens. (2009) (13)
- Synthesis and stereochemistry of latia luciferin (1970) (13)
- Panal: A possible precursor of fungal luciferin (1988) (13)
- The structure and stereochemistry of tetrodotoxin (1963) (12)
- Unique reactivity of the Mukaiyama glycosidation catalyst (SnCl3ClO4) toward beta-mannopyranosides. (2008) (12)
- BIOGENETIC-TYPE SYNTHESIS OF PENICILLIN-CEPHALOSPORIN ANTIBIOTICS PART 1, A STEREOCONTROLLED SYNTHESIS OF THE PENAM- AND CEPHEM-RING SYSTEMS FROM AN ACYCLIC TRIPEPTIDE EQUIVALENT (1975) (12)
- A new synthesis of epidithiapiperazinediones (1976) (12)
- Extension of Pd-Mediated One-Pot Ketone Synthesis to Macrocyclization: Application to a New Convergent Synthesis of Eribulin. (2016) (12)
- New Synthetic Route to the C.14—C.38 Segment of Halichondrins. (1998) (11)
- Synthesis of alcohols from m-fluorophenylsulfones and dialkylboranes: application to the C14-C35 building block of E7389. (2012) (11)
- Product‐Regulation Mechanisms for Fatty Acid Biosynthesis Catalyzed by Mycobacterium smegmatis FAS I (2007) (11)
- Synthesis of the C20-C26 building block of halichondrins via a regiospecific and stereoselective S(N)2' reaction. (2002) (11)
- Synthetic study on echinulin and related compounds. Part II. A stereoselective total synthesis of optically active echinulin (1971) (11)
- Mycolactone cytotoxicity in Schwann cells could explain nerve damage in Buruli ulcer (2017) (11)
- Catalytic homocoupling of aryl, alkenyl, and alkynyl halides with Ni(II)-complexes and zirconocene dichloride (2011) (10)
- A concise synthesis of enantiomerically pure taxane C-ring via the [2,3] wittig rearrangement (1993) (10)
- [Snytheitc studies on echniulin and related natural products. II. A total synthesis of echinulin (author's transl)]. (1977) (10)
- Synthesis and structure of two new mycolactones isolated from M. ulcerans subsp. shinshuense. (2012) (10)
- Complexation of Fatty Acids and Fatty Acid‐CoAs with Synthetic O‐Methylated Polysaccharides (2007) (10)
- Unified Synthesis of C1-C19 Building Blocks of Halichondrins via Selective Activation/Coupling of Polyhalogenated Nucleophiles in (Ni)/Cr-Mediated Reactions. (2015) (10)
- Chiral aggregates formed from methylated tetraenoic fatty acids: formation of both antipodes of chiral aggregates from a single enantiomer and time-dependent stereomutation. (2007) (10)
- Photochemistry of mycolactone A/B, the causative toxin of Buruli ulcer. (2012) (9)
- Novel syntheses of -halo-a,-unsaturated ketones (1995) (9)
- Further studies on the structure of tetrodotoxin (1964) (9)
- [Synthetic studies on echinulin and realted natural products. I. Acid-catalyzed amino-Claisen rearrangement of N-allylaniline and N,N-diallylaniline derivatives (author's transl)]. (1977) (9)
- Solution Structure of n‐Type DNA Oligomers Possessing a Covalently Cross‐Linked Watson–Crick Base Pair Model (2001) (9)
- [Synthetic studies on echinulin and related natural products. III. A total synthesis of neoechinulin (author's transl)]. (1977) (9)
- [Synthetic studies on echinulin and related natural products. VI. Structure and synthesis of aurechinulin (author's transl)]. (1977) (8)
- Luciferine, bioluminescierende Substanzen (1968) (8)
- Dinoflagellate bioluminescence: Chemical behavior of the chromophore towards oxidants (1994) (8)
- Aggregation behavior of tetraenoic fatty acids in aqueous solution. (2007) (8)
- DINOFLAGELLATE BIOLUMINESCENCE : THE CHROMOPHORE OF DINOFLAGELLATE LUCIFERIN (1994) (8)
- Synthetic studies on tetrodotoxin and related compounds. V. The protecting group of the C9-hydroxy group (1974) (8)
- Practical and scalable synthesis of alpha-(1-->4)-linked polysaccharides composed of 6-O-methyl-D-glucose. (2007) (7)
- A USEFUL MODIFICATION OF THE GARST-SPENCER FURAN ANNULATION : AN IMPROVED SYNTHESIS OF 3,4-SUBSTITUTED FURANS (1998) (7)
- Biosynthesis of nigrifactin (1973) (7)
- Stereocontrolled Synthesis of Left Halves of Halichondrins. (2017) (7)
- TOTAL SYNTHESIS OF POLYETHER ANTIBIOTICS NARASIN AND SALINOMYCIN (1982) (6)
- Structure of the C8-Base, an Acid Degradation Product of Tetrodotoxin (1962) (6)
- Unified Synthesis of Right Halves of Halichondrins A-C. (2017) (6)
- [Synthetic studies on echinulin and related natural products. IV. Isolation, structure and synthesis of flavoglaucin-auroglaucin type natural products isolated from Aspergillus amstelodami (author's transl)]. (1977) (6)
- The catalytic action of metal salts on the borohydride reduction of α-bromoketone (1961) (6)
- Studies on the Total Synthesis of Batrachotoxin (2004) (6)
- Novel Structure Elucidation of AAL Toxin TA Backbone. (1994) (6)
- Influence of secondary structure (helical conformation) on stereoselectivity in peptide couplings (1987) (6)
- C-sucrose vs. O-sucrose: Different conformational behavior in methanol solutions containing Ca2+ (1994) (6)
- The stereospecific synthesis of tetrahydroaustamide (1978) (6)
- Structure—Activity Relationships of Halichondrin B Analogues: Modifications at C30—C38. (2000) (6)
- A stereoselective decarboxylation of 1,6-dimethyl-3-(3′-indolyl)methyl-3-carboxy-2,5-piperazinedione (1971) (5)
- [Synthesis of Cypridina luciferin and related compounds. II. Synthesis of etioluciferamine]. (1969) (5)
- Stereoselective total synthesis and stereochemistry confirmation of photo-mycolactones (2015) (5)
- NOVEL, LIGHT-EMITTING REACTION OF (E)-2-(PHENYLSULFONYL)-3-PHENYLOXAZIRIDINE WITH STRONG BASES (1995) (5)
- Design, synthesis, and cytotoxicity of stabilized mycolactone analogs. (2017) (5)
- Structure of the Light Emitter in Krill (Euphausia pacifica) Bioluminescence. (1988) (5)
- Synthetic Lipid A Antagonists for Sepsis Treatment (2005) (5)
- X-Ray structure determination of 3,6-p-anisylidenedithio-3-ethyl-NN′-dimethylpiperazine-2,5-dione (1975) (5)
- BIOGENETIC‐TYPE SYNTHESIS OF PENICILLIN‐CEPHALOSPORIN ANTIBIOTICS PART 2, AN OXIDATIVE CYCLIZATION ROUTE TO BETA‐LACTAM THIAZOLINE DERIVATIVES (1975) (5)
- The stereochemical requirement for protein kinase C activation by 3‐methyldiglycerides matches that found in naturally occurring tumor promoters aplysiatoxins (1990) (5)
- Synthetic studies in the field of natural products (1975) (5)
- Synthesis of leonurine (1968) (5)
- Zr/Ni-Mediated One-Pot Ketone Synthesis (2017) (4)
- Total Synthesis of Palytoxin Carboxylic Acid and Palytoxin Amide. (1990) (4)
- Further Studies on Ni/Zr-mediated One-pot Ketone Synthesis: Use of a Mixture of NiI- and NiII-catalysts Greatly Improves the Molar Ratio of Coupling Partners (2019) (4)
- Hydrolytic cleavage of thiazoline sulfoxides by a radical chain process selective transformation of cooper's β-lactam thiazolines into penicillin sulfoxides (1976) (4)
- Total synthesis and stereochemistry of cytoblastin. (1998) (4)
- Chlorophyll Catabolism Leading to the Skeleton of Dinoflagellate and Krill Luciferins: Hypothesis and Model Studies Financial support from the National Institutes of Health (NS 12108) is gratefully acknowledged. (2001) (4)
- Total Synthesis of Halistatins 1 and 2. (2020) (4)
- A model study for the biomimetic-type synthesis of rifamycin S (1981) (4)
- Ni(II)/Cr(II)-Mediated Coupling Reaction: An Asymmetric Process. (1996) (3)
- Extraction and Purification of Tetrodotoxin (1964) (3)
- Synthetic Studies Towards Batrachotoxin. Part 1. A Furan-Based Intramolecular Diels-Alder Route to Construct the A-D Ring System. (1995) (3)
- Structure of the C9-Base, an Alkaline Degradation Product of Tetrodotoxin (1962) (3)
- A TOTAL SYNTHESIS OF DEHYDROGLIOTOXIN (1973) (3)
- Tetrodotoxin. III. A Revised Molecular Formula for Tetrodotoxin (1964) (3)
- From Luc and Phot genes to the hospital bed. (1990) (3)
- Fe/Cr‐ and Co/Cr‐Mediated Catalytic Asymmetric 2‐Haloallylations of Aldehydes. (2005) (3)
- Dramatic Rate Enhancement of Suzuki Diene Synthesis: Its Application to Palytoxin Synthesis. (1987) (3)
- Extension of the Eschenmoser Sulfide Contraction/Iminoester Cyclization Method to the Synthesis of Tolyporphin Chromophore. (1997) (3)
- Conformational Analysis of C‐Glycosides and Related Compounds: Programming Conformational Profiles of C‐ and O‐Glycosides (2005) (3)
- On Stereochemistry of Osmium Tetroxide Oxidation of Allylic Alcohol Systems: Empirical Rule. On Stereochemistry of Osmium Tetroxide Oxidation of Allylic Alcohol Systems: Examples. (1984) (2)
- Chiral Analogues of Enterobactin with Hydrophilic or Lipophilic Properties. (1993) (2)
- Total Synthesis of (+)-Monensin (1980) (2)
- A STEREOSPECIFIC TOTAL SYNTHESIS OF DL-SAXITOXIN (1977) (2)
- Enantioselective Total Synthesis of Fumonisin B2. (1998) (2)
- Total Synthesis of Altohyrtin A (Spongistatin 1). Part 2. (1998) (2)
- Synthetic Studies Towards Batrachotoxin. Part 2. Formation of the Oxazepane Ring System via a Michael Reaction. (1995) (2)
- Synthesis of Mono and Unsymmetrical Bis Ortho Esters of scyllo-Inositol. (1986) (2)
- Synthetic Study of Puffer-fish Poison, Tetrodotoxin (1975) (2)
- Enantioselective Total Synthesis of (‐)‐Decarbamoylsaxitoxin. (1992) (2)
- Preferred Conformation of C-Glycosides. Part 1. Conformational Similarity of Glycosides and Corresponding C-Glycosides. (1988) (1)
- SYNTHETIC STUDIES ON POLYETHER ANTIBIOTICS. 4. TOTAL SYNTHESIS OF MONENSIN. 1. STEREOCONTROLLED SYNTHESIS OF THE LEFT HALF OF MONENSIN (2002) (1)
- The Structures of Tetrodotoxin and Anhydroepitetrodotoxin (1964) (1)
- FURTHER STUDIES ON STEREOSPECIFIC EPOXIDATION OF ALLYLIC ALCOHOLS (1981) (1)
- Preferred Conformation of C-Glycosides. Part 2. Preferred Conformation of Carbon Analogues of Isomaltose and Gentiobiose. (1988) (1)
- Total Synthesis and Stereo-chemistry of Pinnatoxins B and C (2008) (1)
- Acetylation of Tetrodotoxin (1964) (1)
- Total Synthesis of (.+-.)-Batrachotoxinin A. (1998) (1)
- Total Synthesis of the Proposed Structure of (+)‐Tolyporphin A O,O‐Diacetate. (1999) (1)
- Total Synthesis of Altohyrtin A (Spongistatin 1). Part 1. (1998) (1)
- Relative and Absolute Stereochemistry of the Fumonisin B2 Backbone. (1995) (1)
- Semi-synthetic aequorin (2005) (1)
- Natural Product Synthesis: Palytoxin (1987) (1)
- The Stereochemical Assignment and Conformational Analysis of the V/W- Ring Juncture of Maitotoxin (1997) (1)
- Unified, Efficient, and Scalable Synthesis of Halichondrins, with Use of Zr/Ni-Mediated One-Pot Ketone Synthesis as Final Coupling Reaction (2017) (1)
- SYNTHETIC STUDIES ON HISTRIONICOTOXINS PART 1, A STEREOCONTROLLED SYNTHESIS OF (+-)-PERHYDROHISTRIONICOTOXIN (1975) (1)
- Structure of Tetrodoic Add, a Hydrolysis Product of Tetrodotoxin (1964) (1)
- Extension of the Criegee Rearrangement: Synthesis of Enol Ethers from Secondary Allylic Hydroperoxides. (1995) (1)
- Catalytic Effect of Nickel(II) Chloride and Palladium(II) Acetate on Chromium(II)-Mediated Coupling Reaction of Iodo Olefins with Aldehydes. (1987) (1)
- Total Synthesis of (+)-Ophiobolin C. (1989) (1)
- SYNTHETIC STUDIES ON ECHINULIN AND RELATED NATURAL PRODUCTS. VI. STRUCTURE AND SYNTHESIS OF AURECHINULIN (1977) (1)
- Steroid Studies. III. A New Route for the Preparation of Cholestane-3β, 5α, 6α-triol 3,6-Diacetate from Cholesterol (1962) (1)
- A NEW METHOD FOR THE SYNTHESIS OF EPIDITHIODIKETOPIPERAZINES (1973) (1)
- Further Synthetic Studies on Rifamycin S. (1982) (1)
- Stereochemical Assignment of the C21—C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction. (2001) (1)
- Synthetic approach towards tetrodotoxin. I. Diels-Alder reaction of alpha-oximinoethylbenzooquinones with butadiene. (1970) (1)
- Synthetic Studies on Halichondrins: A Practical Synthesis of the C1- C13 Segment. (1997) (1)
- Synthesis of C-Sucrose. (1988) (1)
- A New, Efficient Synthesis of the Left Half of Narasin (I). (1987) (0)
- Abstract 4183: Mechanism of action analysis of anti-CAF activity of E7130, a novel tumor-microenvironment ameliorator (2020) (0)
- SYNTHETIC STUDIES ON TETRODOTOXIN AND RELATED COMPOUNDS PART 5, THE PROTECTING GROUP OF THE C9-HYDROXY GROUP (1974) (0)
- TOTAL SYNTHESIS OF RIFAMYCINS. 1. STEREOCONTROLLED SYNTHESIS OF THE ALIPHATIC C BUILDING BLOCK (1981) (0)
- Conformational analysis of a covalently cross-linked Watson-Crick base pair model. (2008) (0)
- HYDROLYTIC CLEAVAGE OF THIAZOLINE SULFOXIDES BY A RADICAL CHAIN PROCESS. SELECTIVE TRANSFORMATION OF COOPER′S β-LACTAM THIAZOLINES INTO PENICILLIN SULFOXIDES (1976) (0)
- Synthesis of C-Disaccharides (I). (1987) (0)
- S-3 Total Synthesis of Tetrodotoxin : Stereochemistry Control in Organic Synthesis (2008) (0)
- Preferred Conformation of C-Glycosides. Part 3. Preferred Conformation of Carbon Analogues of 1,4-Disaccharides. (1988) (0)
- Aldol Reaction of Allenolates Generated via 1,4-Addition of Iodide Anion or Its Equivalent to αβ-Acetylenic Ketones. (1987) (0)
- SYNTHETIC STUDIES TOWARD MITOMYCINS. III. TOTAL SYNTHESES OF MITOMYCINS A AND D C (1978) (0)
- Novel Syntheses of β-Halo-α,β-unsaturated Ketones. (1995) (0)
- P-221 Unified Total Synthesis and Stereochemistry of Pteriatoxins A-C and Pinnatoxins B/C (2006) (0)
- A Practical Synthesis of trans-Iodoolefins. (1987) (0)
- β-Selective C-Glycosidations: Lewis-Acid Mediated Reactions of Carbohydrates with Silyl Ketene Acetals. (1997) (0)
- Dinoflagellate Bioluminescence: Chemical Behavior of the Chromophore Towards Oxidants. (1995) (0)
- PL-1 THE HALICHONDRINS, ANTI-TUMOR MARINE NATURAL PRODUCTS : A STORY BY AN ACADEMICIAN (2006) (0)
- E-1-3 The Structure and Stereochemistry of Tetrodotoxin(Mainly physico-chemical methods) (1964) (0)
- Structure of C9-Base, C8-Base and Oxy-C8-Base, Alkaline and Acid Degradation Products of Tetrodotoxin and its Derivatives (1964) (0)
- Validation of Lanthanoid Chiral Shift Reagents for Determination of Absolute Configuration: Total Synthesis of Glisoprenin A. (2005) (0)
- Total Synthesis of Debromoaplysiatoxin and Aplysiatoxin. (1988) (0)
- Toward Creation of a Universal NMR Database for Stereochemical Assignment: The Case of 1,3,5-Trisubstituted Acyclic Systems (I) and (II). (2000) (0)
- REDUCTIVE RING OPENINGS OF ALLYL ALCOHOL EPOXIDES (1982) (0)
- Preferred Conformation of C‐Glycosides. Part 10. Synthesis and Conformation Analysis of Carbon Trisaccharides. (1992) (0)
- Synthesis of DNA Oligomers Possessing a Covalently Cross-Linked Watson-Crick Base Pair Model Financial support from the National Institutes of Health (Grant: NS 12108) is gratefully acknowledged. (2001) (0)
- Investigations of the Intramolecular Ni(II)/Cr(II)-Mediated Coupling Reaction: Application to the Taxane Ring System. (1994) (0)
- グリオトキシン,デヒドログリオトキシン,ハイアロデンドリンの全合成 (1981) (0)
- A landmark in drug discovery based on complex natural product synthesis (2019) (0)
- SYNTHETIC STUDIES ON POLYETHER ANTIBIOTICS. III. A STEREOCONTROLLED SYNTHESIS S OF ISOLASALOCID KETONE FROM ACYCLIC PRECURSORS (1978) (0)
- Synthetic Endotoxin Antagonists (2020) (0)
- Surprisingly Efficient Catalytic Cr-Mediated Reactions (2006) (0)
- Use of a Chiral Praseodymium Shift Reagent in Predicting the Complete Stereostructure of Glisoprenin A (2005) (0)
- SYNTHETIC STUDIES ON ECHINULIN AND RELATED NATURAL PRODUCTS. I. ACID‐CATALYZED AMINO‐CLAISEN REARRANGEMENT OF N‐ALLYLANILINE AND N,N‐DIALLYLANILINE DERIVATIVES (1977) (0)
- IUPAC TOTAL SYNTHESIS OF RIFAMYCIN S (2006) (0)
- SYNTHETIC STUDIES ON HISTRIONICOTOXINS PART 2, A PRACTICAL SYNTHETIC ROUTE TO (+-)-PERHYDRO- AND (+-)-OCTAHYDROHISTRIONICOTOXIN (1975) (0)
- A TOTAL SYNTHESIS OF GLIOTOXIN (1977) (0)
- Complexation of Fatty Acids and Fatty Acids‐CoAs with Synthetic O‐Methylated Polysaccharides (2007) (0)
- Palytoxin: An Inexhaustible Source of Inspiration — Personal Perspective (2002) (0)
- Halikondriinit and closely related compounds (1994) (0)
- Abstract 1865: Tumor microenvironment ameliorating effect of E7130 sensitized ER+ breast cancer against fulvestrant (2022) (0)
- One‐Pot Ketone Synthesis with Alkylzinc Halides Prepared from Alkyl Halides Via a Single Electron Transfer (SET) Process: New Extension of Fukuyama Ketone Synthesis. (2016) (0)
- Preferred Conformation of C-Glycosides. Part 8. Synthesis of 1,4- Linked Carbon Disaccharides. (1992) (0)
- CYPRIDINA BIOLUMINESCENCE PART 9, TAUTOMERIC STRUCTURES OF 2-METHYL-3,7-DIHYDROIMIDAZO(1,2-A)PYRAZIN-3-ONE, 2-METHYL-3-AMINOIMIDAZO(1,2-A)PYRAZINE AND THEIR DERIVATIVES IN NEUTRAL AND ACIDIC MEDIA (1975) (0)
- Panal: A Possible Precursor of Fungal Luciferin. (1988) (0)
- A Mild Preparation of Vinyl Iodides from Vinylsilanes. (1997) (0)
- NOVEL SYNTHESESOF BETA -HALO-ALPHA ,BETA -UNSATURATED KETONES (1995) (0)
- Applications of Ni(II)/Cr(II)‐Mediated Coupling Reactions to Natural Products Syntheses (1992) (0)
- Surprisingly Efficient Catalytic Cr‐Mediated Coupling Reactions. (2006) (0)
- PEANUT LECTIN COMPLEXED WITH C-LACTOSE (1998) (0)
- Preferred Conformation of C‐Glycosides. Part 13. A Comparison of the Conformational Behavior of Several C‐, N‐, and O‐Furanosides. (1995) (0)
- Synthesis of Alcohols from m‐Fluorophenylsulfones and Dialkylboranes: Application to the C14—C35 Building Block of E7389. (2012) (0)
- SYNTHETIC STUDIES ON POLYETHER ANTIBIOTICS. II. STEREOCONTROLLED SYNTHESES OF F EPOXIDES OF BISHOMOALLYLIC ALCOHOLS (1978) (0)
- A Concise Synthesis of Enantiomerically Pure Taxane C-Ring via the (2, 3) Wittig Rearrangement. (1994) (0)
- Dinoflagellate Bioluminescence: The Chromophore of Dinoflagellate Luciferin. (1995) (0)
- Total Synthesis of a Fully Protected Palytoxin Carboxylic Acid. (1990) (0)
- Publications: Yoshito Kishi (2007) (0)
- Total Synthesis and Stereochemistry of Cytoblastin (I). (1996) (0)
- Reaction of Methylcerium Reagent with Tertiary Amides: Synthesis of Saturated and Unsaturated Ketones from Tertiary Amides. (1998) (0)
- Total Synthesis and Stereochemistry of Mycolactone F (I). (2008) (0)
- A TOTAL SYNTHESIS OF SPORIDESMIN A (1973) (0)
- A NOVEL TYPE OF ADDUCTS IN THE PHOTOCHEMICAL REACTIONS OF O-CHLORANIL WITH ALDEHYDES (1975) (0)
- Preferred Conformation of C-Glycosides. Part 4. Importance of 1,3-Diaxial-Like Interactions Around the Nonglycosidic Bond: Prediction and Experimental Proof. (1989) (0)
- CYPRIDINA BIOLUMINESCENCE PART 8, THE BIOLUMINESCENCE OF CYPRIDINA LUCIFERIN ANALOGS (1973) (0)
- Lipid A Antagonist Response by E5531, a Novel Synthetic Suppression of Murine Endotoxin (2013) (0)
- A Useful Modification of the Garst‐Spencer Furan Annulation: An Improved Synthesis of 3,4‐Substituted Furans. (1999) (0)
- A Total Synthesis of D,L-Histrionicotoxin (I). (1986) (0)
- β-Halovinyl Ketones: Synthesis from Acetylenic Ketones. (1987) (0)
- Preferred Conformation of C-Glycosides. Part 12. Synthesis and Conformational Analysis of α,α-, α,β-, and . beta.,β-C-Trehaloses (1994) (0)
- P-452 DEVELOPMENT OF PRACTICAL SYNTHESIS OF HALICHONDIRINS (2006) (0)
- EINE STEREOSELEKTIVE DECARBOXYLIERUNG VON 1,6-DIMETHYL-3-(3′-INDOLYL)-METHYL-3-CARBOXY-2,5-PIPERAZIN-DION (1972) (0)
- Synthetic Studies Toward the Taxane Class of Natural Products. (1994) (0)
- In Vitro and In Vivo Anticancer Activities of Synthetic Macrocyclic Ketone Analogues of Halichondrin B 1 (2001) (0)
- Further Improvement on Sulfonamide‐Based Ligand for Catalytic Asymmetric 2‐Haloallylation and Allylation. (2008) (0)
- Abstract 4179: E7130 derived from total synthesis of halichondrin as a novel tumor-microenvironment ameliorator (2020) (0)
- Research summary of Kishi group (This volume is dedicated to Prof. Yoshito Kishi on the occasion of his 70th birthday) (2007) (0)
- A Total Synthesis of Polyether Antibiotic (-)-A23187 (Calcimycin). (1987) (0)
- SYNTHETIC STUDIES ON PALYTOXIN. STEREOCONTROLLED, PRACTICAL SYNTHESIS OF THE C-101-C-115 SEGMENT (1983) (0)
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