Valery V. Fokin
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American chemist
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Valery V. Fokinchemistry Degrees
Chemistry
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Physical Chemistry
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Organic Chemistry
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Chemistry
Valery V. Fokin's Degrees
- PhD Chemistry University of Southern California
- Masters Chemistry University of Southern California
- Bachelors Chemistry Moscow State University
Why Is Valery V. Fokin Influential?
(Suggest an Edit or Addition)Valery V. Fokin's Published Works
Number of citations in a given year to any of this author's works
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
- A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. (2002) (8851)
- Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides. (2010) (1522)
- Bioconjugation by copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition. (2003) (1359)
- Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. (2004) (1345)
- "On water": unique reactivity of organic compounds in aqueous suspension. (2005) (1288)
- Organic synthesis "on water". (2009) (1250)
- Polytriazoles as copper(I)-stabilizing ligands in catalysis. (2004) (1174)
- Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(i)-catalyzed ligation of azides and alkynes. (2004) (980)
- Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism. (2008) (643)
- Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-Catalyzed Azide-Alkyne Cycloadditions (2013) (566)
- Mechanism of the ligand-free CuI-catalyzed azide-alkyne cycloaddition reaction. (2005) (486)
- A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction. (2004) (472)
- Inhibitors of HIV-1 protease by using in situ click chemistry. (2006) (447)
- Catalytic Azide—Alkyne Cycloaddition: Reactivity and Applications (2007) (415)
- Multivalent, bifunctional dendrimers prepared by click chemistry. (2005) (371)
- A Potent and Highly Selective Inhibitor of Human α-1,3-Fucosyltransferase via Click Chemistry (2003) (369)
- Rhodium-catalyzed transannulation of 1,2,3-triazoles with nitriles. (2008) (354)
- Click chemistry in materials synthesis. 1. Adhesive polymers from copper‐catalyzed azide‐alkyne cycloaddition (2004) (346)
- Ligand-accelerated Cu-catalyzed azide-alkyne cycloaddition: a mechanistic report. (2007) (334)
- Structurally diverse dendritic libraries : A highly efficient functionalization approach using Click chemistry (2005) (296)
- Discovery and characterization of catalysts for azide-alkyne cycloaddition by fluorescence quenching. (2004) (294)
- Lipoxin A4 Stable Analogs Are Potent Mimetics That Stimulate Human Monocytes and THP-1 Cells via a G-protein-linked Lipoxin A4 Receptor* (1997) (286)
- One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated azides. (2004) (285)
- Ruthenium-catalyzed cycloaddition of alkynes and organic azides. (2006) (263)
- Ruthenium-catalyzed cycloaddition of aryl azides and alkynes. (2007) (258)
- Copper-catalyzed synthesis of N-sulfonyl-1,2,3-triazoles: controlling selectivity. (2007) (251)
- Click chemistry: function follows form. (2010) (245)
- Rhodium-catalyzed enantioselective cyclopropanation of olefins with N-sulfonyl 1,2,3-triazoles. (2009) (224)
- Direct synthesis of 1,5-disubstituted-4-magnesio-1,2,3-triazoles, revisited. (2004) (219)
- Efficient synthesis of 1-sulfonyl-1,2,3-triazoles. (2010) (214)
- Practical synthesis of amides from in situ generated copper(I) acetylides and sulfonyl azides. (2006) (206)
- One-pot copper(I)-catalyzed synthesis of 3,5-disubstituted isoxazoles. (2005) (191)
- Transannulation of 1-sulfonyl-1,2,3-triazoles with heterocumulenes. (2013) (190)
- Transition-metal-free catalytic synthesis of 1,5-diaryl-1,2,3-triazoles. (2010) (190)
- Rapid discovery and structure-activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper(I)-catalyzed synthesis of 1,2,3-triazoles and their further functionalization. (2006) (186)
- Sulfonyl-1,2,3-triazoles: convenient synthones for heterocyclic compounds. (2013) (182)
- Enhanced Reactivity of Dinuclear Copper(I) Acetylides in Dipolar Cycloadditions (2007) (178)
- Stereoselective 1,3-insertions of rhodium(II) azavinyl carbenes. (2014) (169)
- Synthesis and reactivity of rhodium(II) N-triflyl azavinyl carbenes. (2010) (169)
- Mechanistic studies on the Cu-catalyzed three-component reactions of sulfonyl azides, 1-alkynes and amines, alcohols, or water: dichotomy via a common pathway. (2008) (168)
- Catalytic asymmetric C-H insertions of rhodium(II) azavinyl carbenes. (2011) (166)
- SuFEx-based synthesis of polysulfates. (2014) (152)
- Arylation of rhodium(II) azavinyl carbenes with boronic acids. (2012) (141)
- Efficient synthesis of 2-substituted-1,2,3-triazoles. (2008) (140)
- Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks (2002) (140)
- Ruthenium-catalyzed cycloaddition of nitrile oxides and alkynes: practical synthesis of isoxazoles. (2008) (138)
- Bringing Efficiency to Materials Synthesis: The Philosophy of Click Chemistry (2007) (133)
- Rapid Diversity‐Oriented Synthesis in Microtiter Plates for In Situ Screening of HIV Protease Inhibitors (2003) (126)
- Copper-catalyzed reaction cascade: direct conversion of alkynes into N-sulfonylazetidin-2-imines. (2006) (121)
- Copper(I)-catalyzed cycloaddition of organic azides and 1-iodoalkynes. (2010) (120)
- Catalytic asymmetric transannulation of NH-1,2,3-triazoles with olefins. (2014) (119)
- Iterative in situ click chemistry creates antibody-like protein-capture agents. (2009) (118)
- Polyisoprenyl phosphate (PIPP) signaling regulates phospholipase D activity: a ‘stop’ signaling switch for aspirin‐triggered lipoxin A4 (1999) (117)
- Ring expansion and rearrangements of rhodium(II) azavinyl carbenes. (2012) (106)
- Polytriazoles as Copper(I)‐Stabilizing Ligands in Catalysis. (2004) (105)
- New Structural Scaffolds for Centrally Acting Oxime Reactivators of Phosphylated Cholinesterases* (2011) (104)
- Lipoxin B4 regulates human monocyte/neutrophil adherence and motility: design of stable lipoxin B4 analogs with increased biologic activity (1998) (99)
- Kinetic resolution by copper-catalyzed azide–alkyne cycloaddition (2005) (98)
- Role of Architecture and Molecular Weight in the Formation of Tailor-Made Ultrathin Multilayers Using Dendritic Macromolecules and Click Chemistry (2007) (94)
- Refinement of Structural Leads for Centrally Acting Oxime Reactivators of Phosphylated Cholinesterases* (2012) (90)
- The allylic azide rearrangement: achieving selectivity. (2005) (87)
- Ruthenium-catalyzed cycloadditions of 1-haloalkynes with nitrile oxides and organic azides: synthesis of 4-haloisoxazoles and 5-halotriazoles. (2014) (85)
- Click chemistry in materials synthesis. III. Metal‐adhesive polymers from Cu(I)‐catalyzed azide–alkyne cycloaddition (2007) (81)
- Ultrasound-promoted copper-catalyzed azide-alkyne cycloaddition. (2010) (75)
- Selective and Orthogonal Post-Polymerization Modification using Sulfur(VI) Fluoride Exchange (SuFEx) and Copper-Catalyzed Azide–Alkyne Cycloaddition (CuAAC) Reactions (2016) (73)
- Polymer-Supported Copper(I) Catalysts for the Experimentally Simplified Azide–Alkyne Cycloaddition (2007) (73)
- Imidazole Aldoximes Effective in Assisting Butyrylcholinesterase Catalysis of Organophosphate Detoxification (2014) (72)
- NH-1,2,3-Triazole-based Inhibitors of the VIM-2 Metallo-β-Lactamase: Synthesis and Structure-Activity Studies. (2010) (71)
- Halogen exchange (Halex) reaction of 5-iodo-1,2,3-triazoles: synthesis and applications of 5-fluorotriazoles. (2012) (70)
- Reactivity of N-(1,2,4-triazolyl)-substituted 1,2,3-triazoles. (2011) (68)
- LXA4, aspirin-triggered 15-epi-LXA4, and their analogs selectively downregulate PMN azurophilic degranulation. (1999) (68)
- Generation of candidate ligands for nicotinic acetylcholine receptors via in situ click chemistry with a soluble acetylcholine binding protein template. (2012) (66)
- Centrally acting oximes in reactivation of tabun-phosphoramidated AChE. (2013) (65)
- Disubstituted Sialic Acid Ligands Targeting Siglecs CD33 and CD22 Associated with Myeloid Leukaemias and B Cell Lymphomas. (2014) (64)
- A Mass Spectrometry Plate Reader: Monitoring Enzyme Activity and Inhibition with a Desorption/Ionization on Silicon (DIOS) Platform (2004) (63)
- Design, synthesis and bioactions of novel stable mimetics of lipoxins and aspirin-triggered lipoxins. (2005) (63)
- Copper(I)-catalyzed cycloaddition of bismuth(III) acetylides with organic azides: synthesis of stable triazole anion equivalents. (2013) (62)
- A New Approach to Osmium‐Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins (2002) (60)
- Click and pick: identification of sialoside analogues for siglec-based cell targeting. (2012) (60)
- Synthesis and electrochemistry of 2-ethenyl and 2-ethanyl derivatives of 5-nitroimidazole and antimicrobial activity against Giardia lamblia. (2009) (59)
- Oxime-assisted Acetylcholinesterase Catalytic Scavengers of Organophosphates That Resist Aging* (2011) (55)
- Rhodium(II)-catalyzed asymmetric sulfur(VI) reduction of diazo sulfonylamidines. (2012) (55)
- Synthesis and Postpolymerization Functionalization of Poly(5-iodo-1,2,3-triazole)s (2011) (54)
- Expanded therapeutic potential in activity space of next-generation 5-nitroimidazole antimicrobials with broad structural diversity (2013) (52)
- Synthesis and reactivity of sulfamoyl azides and 1-sulfamoyl-1,2,3-triazoles. (2011) (50)
- On-chip synthesis and screening of a sialoside library yields a high affinity ligand for Siglec-7. (2013) (49)
- Copper-Catalyzed Azide—Alkyne Cycloaddition (CuAAC) and Beyond: New Reactivity of Copper(I) Acetylides (2010) (47)
- Click imaging of biochemical processes in living systems. (2007) (45)
- The chemistry of zerumbone. Part 5: Structural transformation of the dimethylamine derivatives (2003) (43)
- Identification of a new endogenous metabolite and the characterization of its protein interactions through an immobilization approach. (2009) (42)
- Novel VEGFR-2 kinase inhibitors identified by the back-to-front approach. (2013) (42)
- Inhibitors of VIM-2 by screening pharmacologically active and click-chemistry compound libraries. (2009) (41)
- A Practical and Highly Efficient Aminohydroxylation of Unsaturated Carboxylic Acids (2001) (41)
- Selective Formation of 1,4-Disubstituted Triazoles from Ruthenium-Catalyzed Cycloaddition of Terminal Alkynes and Organic Azides: Scope and Reaction Mechanism (2012) (41)
- Catalytic Soman Scavenging by the Y337A/F338A Acetylcholinesterase Mutant Assisted with Novel Site-Directed Aldoximes. (2015) (40)
- From BACE1 Inhibitor to Multifunctionality of Tryptoline and Tryptamine Triazole Derivatives for Alzheimer’s Disease (2012) (39)
- Cu‐Catalyzed Azide‐Alkyne Cycloaddition: Preparation of Tris((1‐Benzyl‐1H‐1,2,3‐Triazolyl)Methyl)Amine (2012) (39)
- Efficient synthesis of sulfonyl azides from sulfonamides. (2008) (38)
- Synthesis and biological evaluation of furanoallocolchicinoids. (2015) (38)
- Lipoxin a 4 Stable Analogs Are Potent Mimetics That Stimulate Human Monocytes and THP-1 Cells via a G-protein-linked Lipoxin a 4 Receptor (1997) (37)
- Regioselective Synthesis of Fluorosulfonyl 1,2,3-Triazoles from Bromovinylsulfonyl Fluoride. (2018) (37)
- A very large diversity space of synthetically accessible compounds for use with drug design programs (2005) (33)
- Pharmacology, Pharmacokinetics, and Tissue Disposition of Zwitterionic Hydroxyiminoacetamido Alkylamines as Reactivating Antidotes for Organophosphate Exposure (2018) (31)
- A potent and highly selective inhibitor of human alpha-1,3-fucosyltransferase via click chemistry. (2003) (29)
- Mechanism of interaction of novel uncharged, centrally active reactivators with OP-hAChE conjugates. (2013) (27)
- Sulfuryl Fluoride Mediated Conversion of Aldehydes to Nitriles. (2019) (26)
- Selectivity optimization of substituted 1,2,3-triazoles as α7 nicotinic acetylcholine receptor agonists. (2015) (26)
- Synthesis of 7-aza-5-deazapurine analogues via copper(I)-catalyzed hydroamination of alkynes and 1-iodoalkynes. (2010) (25)
- Spectroscopic, crystallographic and computational studies of the formation and isomerization of cyclic acetals and ketals of pentonolactones ☆ (1994) (23)
- Interaction kinetics of oximes with native, phosphylated and aged human acetylcholinesterase. (2010) (22)
- Catalyst Activation, Chemoselectivity, and Reaction Rate Controlled by the Counterion in the Cu(I)-Catalyzed Cycloaddition between Azide and Terminal or 1-Iodoalkynes (2018) (22)
- Synthesis of Selective Agonists for the α7 Nicotinic Acetylcholine Receptor with In Situ Click-Chemistry on Acetylcholine-Binding Protein Templates (2012) (21)
- CuAAC: The Quintessential Click Reaction (2012) (21)
- Cover Picture: “On Water”: Unique Reactivity of Organic Compounds in Aqueous Suspension (Angew. Chem. Int. Ed. 21/2005) (2005) (20)
- Triazolyl tryptoline derivatives as β-secretase inhibitors. (2010) (20)
- Synthesis of Indole-Derived Allocolchicine Congeners through Pd-Catalyzed Intramolecular C-H Arylation Reaction (2014) (19)
- Osmium-Catalyzed Olefin Dihydroxylation and Aminohydroxylation in the Second Catalytic Cycle (2006) (19)
- Chemistry ‘On Water’ – Organic Synthesis in Aqueous Suspension (2007) (19)
- Copper‐Catalyzed Azide‐Alkyne Cycloaddition (CuAAC) (2010) (18)
- Reversal of Tabun Toxicity Enabled by a Triazole-Annulated Oxime Library-Reactivators of Acetylcholinesterase. (2019) (18)
- Synthesis of 1,4-triazole linked zanamivir dimers as highly potent inhibitors of influenza A and B (2013) (17)
- NH-1,2,3-Triazoles from Azidomethyl Pivalate and Carbamates: Base-Labile N-Protecting Groups (2005) (14)
- Rhodium‐Catalyzed Transannulation of 1,2,3‐Triazoles with Nitriles. (2009) (14)
- Cognitive improvements in a mouse model with substituted 1,2,3-triazole agonists for nicotinic acetylcholine receptors. (2015) (14)
- REGIOSELECTIVE SYNTHESIS OF EITHER 1H- OR 2H-1,2,3- TRIAZOLES VIA MICHAEL ADDITION TO α,ß-UNSATURATED KETONES. (2008) (14)
- Antiviral Stilbene 1,2-Diamines Prevent Initiation of Hepatitis C Virus RNA Replication at the Outset of Infection (2011) (14)
- Polymer‐Supported Copper(I) Catalysts for the Experimentally Simplified Azide—Alkyne Cycloaddition. (2008) (12)
- Synthesis and evaluation of 1-(substituted)-3-prop-2-ynylureas as antiangiogenic agents. (2012) (11)
- NH‐1,2,3‐Triazoles from Azidomethyl Pivalate and Carbamates: Base‐Labile N‐Protecting Groups. (2006) (11)
- Multivalent, Bifunctional Dendrimers Prepared by Click Chemistry (2006) (10)
- Epoxides and Aziridines in Click Chemistry (2006) (10)
- Titelbild: “On Water”: Unique Reactivity of Organic Compounds in Aqueous Suspension (Angew. Chem. 21/2005) (2005) (10)
- A Microwave‐Assisted Click Chemistry Synthesis of 1,4‐Disubstituted 1,2,3‐Triazoles via a Copper(I)‐Catalyzed Three‐Component Reaction. (2005) (9)
- Cover Picture: Efficiency and Fidelity in a Click‐Chemistry Route to Triazole Dendrimers by the Copper(I)‐Catalyzed Ligation of Azides and Alkynes (Angew. Chem. Int. Ed. 30/2004) (2004) (9)
- NH-1,2,3-Triazole Inhibitors of the VIM-2 Metallo-β-Lactamase (2010) (9)
- Preparation of 1,5-Disubstituted 1,2,3-Triazoles via Ruthenium-catalyzed Azide Alkyne Cycloaddition. (2014) (8)
- Counteracting tabun inhibition by reactivation by pyridinium aldoximes that interact with active center gorge mutants of acetylcholinesterase (2019) (8)
- A Stepwise Huisgen Cycloaddition Process: Copper(I)‐Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes. (2002) (7)
- Sulfuryl Fluoride Mediated Synthesis of Amides and Amidines from Ketoximes via Beckmann Rearrangement. (2020) (7)
- Click chemistry-facilitated comprehensive identification of proteins adducted by antimicrobial 5-nitroimidazoles for discovery of alternative drug targets against giardiasis (2020) (6)
- Synthesis of Fluorescent Boron Difluoride Complexes of 3-Acyl-4-hydroxycoumarins (2014) (6)
- Neuritogenic activity of bi-functional bis-tryptoline triazole. (2017) (6)
- A new approach to osmium-catalyzed asymmetric dihydroxylation and aminohydroxylation of olefins. (2002) (6)
- Negishi Cross-Coupling Reaction as a Route to Isocombretastatins (2013) (6)
- Gold(I) Phosphine Derivatives with Improved Selectivity as Topically Active Drug Leads to Overcome 5-Nitroheterocyclic Drug Resistance in Trichomonas vaginalis. (2021) (5)
- Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks. (2002) (5)
- Synthesis and antitumor activity of 7-(triazol-1-yl)pyrroloallocolchicine derivatives (2015) (5)
- Titelbild: Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes (Angew. Chem. 30/2004) (2004) (4)
- Quantitative Structure-Price Relationship (QS$R) Modeling and the Development of Economically Feasible Drug Discovery Projects (2019) (4)
- On-Water Selectivity Switch in Microdroplets in the 1,2,3-Triazole Synthesis from Bromoethenesulfonyl Fluoride. (2021) (4)
- LXA4, aspirin-triggered 15-epi-LXA4, and their analogs selectively downregulate PMN azurophilic degranulation. (1999) (4)
- Copper‐Catalyzed Synthesis of N‐Sulfonyl‐1,2,3‐triazoles: Controlling Selectivity. (2007) (4)
- Click Chemistry-Facilitated Structural Diversification of Nitrothiazoles, Nitrofurans, and Nitropyrroles Enhances Antimicrobial Activity against Giardia lamblia (2017) (4)
- One‐Pot Copper(I)‐Catalyzed Synthesis of 3,5‐Disubstituted Isoxazoles. (2006) (3)
- Conductive dendrimers obtained by click chemistry (2010) (3)
- Catalytic Dipolar Cycloadditions of Alkynes with Azides and Nitrile Oxides (2010) (3)
- On-Water Reactions (2012) (2)
- A New Approach to Osmium‐Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins. (2002) (2)
- Between Science and Big Business: Tapping Mary Jane’s Uncharted Potential (2022) (2)
- Catalytic Asymmetric C-H Insertions of Rhodium(II)Azavinyl Carbenes (2011) (1)
- Freeze‐Frame Click‐Chemistry Synthesis on a Soluble Alpha‐7 Nicotinic Acetylcholine Receptor (nAChR) Ligand Binding Domain (2008) (1)
- Probing reactivation of tabun phosphylated cholinesterases by mutagenesis and new oximes (2011) (1)
- rapid communication LXA 4 , aspirin-triggered 15-epi-LXA 4 , and their analogs selectively downregulate PMN azurophilic degranulation (1999) (1)
- Irish society of gastroenterology (1998) (1)
- SuFEx based click chemistry for peptide stapling (2018) (1)
- A Concept for the Regioselective Synthesis of 1,2,3-Triazoles (2006) (0)
- Generation of selective ligands for nicotinic acetylcholine receptors (2012) (0)
- Osmium‐Catalyzed Olefin Dihydroxylation and Aminohydroxylation in the Second Catalytic Cycle. (2006) (0)
- Aziridine and Oxirane Ring Openings “On Water” (2014) (0)
- Molecular Determinants of Reactivation Potency for Novel, Efficacious, Centrally Active Oxime Reactivators of Phosphylated Acetylcholinesterase (2012) (0)
- A study of the structure of the shales of the Pula deposit by the ozonization method (1985) (0)
- Passerini and Ugi Reactions (2012) (0)
- Efficient Synthesis of 1‐Sulfonyl‐1,2,3‐triazoles. (2011) (0)
- Special Techniques withWater (2012) (0)
- Dual Electrospray Ionization Enhancement of Proteins Enabled by DMSO Supercharging Reagent. (2021) (0)
- Characterizing the therapeutic efficacy of novel oximes synthesized by click chemistry against organophosphorous compounds poisoning (2010) (0)
- Copper‐Catalyzed Reaction Cascade: Direct Conversion of Alkynes into N‐Sulfonylazetidin‐2‐imines. (2006) (0)
- Transformations Catalyzed by Transition Metals (2012) (0)
- Structure-Reactivity Relationships in "Special" 2nd Cycle Osmium Catalyzed Amino Hydroxylation (2003) (0)
- Nucleophilic Substitution Reactions (2012) (0)
- Rhodium-Catalyzed Enantioselective Cyclopropanation of Olefins (2010) (0)
- CHEMICAL TOOL FOR DECIPHERING COMPLEXITY (2018) (0)
- Synthesizing Selective Agonists for the α 7 Nicotinic Receptor with in situ Click-Chemistry on Acetylcholine Binding Protein Templates (2012) (0)
- Copper ligation of azides and acetylenes (2003) (0)
- In vitro screening of acetylcholinesterase reactivating potency and oxime assisted organophosphate hydrolysis for a library of novel oxime reactivators synthesized by “click‐chemistry”. (2008) (0)
- From BACE 1 Inhibitor to Multifunctionality of Tryptoline and Tryptamine Triazole Derivatives for Alzheimer ’ s Disease (2012) (0)
- Rh(II)-Catalyzed Transannulation of [nl]1,2,3-Triazoleswith Nitriles (2009) (0)
- Electrochemical Studies of the Cycloaddition Activity of Bismuth(III) Acetylides Towards Organic Azides Under Copper(I)-Catalyzed Conditions (2022) (0)
- RS194B pharmacokinetics and antidotal potential in mice exposed to VX and sarin (2018) (0)
- Click Chemistry , 1 , 2 , 3-Triazoles as Selective and Potent α 7 Nicotinic Acetylcholine Receptor Agonists * (2014) (0)
- Synthesis and Reactivity of Sulfamoyl Azides and 1‐Sulfamoyl‐1,2,3‐triazoles. (2012) (0)
- Sulfonyl‐1,2,3‐triazoles: Convenient Synthones for Heterocyclic Compounds. (2013) (0)
- Refinement of structural leads for centrally acting oxime reactivators of phosphylated cholinesterases. (2012) (0)
- New Reactions of Copper Acetylides: Catalytic Dipolar Cycloadditions and Beyond (2010) (0)
- Derivatives of 1,2,3‐triazole lead found to be selective and potent agonists at the α7 nicotinic acetylcholine receptor (1059.8) (2014) (0)
- Soluble templates for drug design: the acetylcholine binding proteins and freeze‐frame, “click” chemistry for in situ synthesis of nicotinic ligands (2008) (0)
- A structure‐guided design strategy to develop ligands with subtype selectivity for human nicotinic acetylcholine receptors (2009) (0)
- Synthesis of Indole-Derived Allocolchicine Congeners Through Pd-Catalyzed Intramolecular C—H Arylation Reaction. (2015) (0)
- Rhodium-Catalyzed Asymmetric Cyclopropanation via AzavinylCarbenoids (2010) (0)
- Diels–Alder Reactions (2012) (0)
- Cycloadditions of Azodicarboxylates (2012) (0)
- Ligand design for human nicotinic acetylcholine receptors using in situ freeze‐frame click chemistry (2010) (0)
- Transannulation of 1‐Sulfonyl‐1,2,3‐triazoles with Heterocumulenes. (2013) (0)
- Chimie a haute affinite pour la production de dendrimeres triazoles (2005) (0)
- Oxidations and Reductions (2012) (0)
- Use of 1,2,4-Triazolyl-1,2,3-Triazoles as Carbene Precursors (2011) (0)
- Catalytic soman scavenging by non-aging acetylcholinesterase mutant assisted with novel site-directed aldoximes (2017) (0)
- Cover Picture: A Mass Spectrometry Plate Reader: Monitoring Enzyme Activity and Inhibition with a Desorption/Ionization on Silicon (DIOS) Platform (ChemBioChem 7/2004) (2004) (0)
- Ligation of azides and acetylenes catalyzed by copper (2003) (0)
- Synthesis of 1,5-Diaryl-1,2,3-triazoles Under Transition-Metal-FreeConditions (2010) (0)
- Design of Novel Oxime Reactivators and Direct Characterization of Their Interaction With OP‐ChE Conjugates (2010) (0)
- The products of the oxidation of Moscow basin boghead (1983) (0)
- AZIDE-BEARING AMINO ACIDS IN PROTEIN ENGINEERING AND (2005) (0)
- Nucleophilic Opening of Three-Membered Rings (2012) (0)
- Ruthenium-Catalyzed Cycloaddition of 1-Haloalkynes with Nitrile Oxides and Organic Azides; Synthesis of 4-Halo Isoxazoles and 5-Halo Triazoles (2015) (0)
- Coupling Reactions of Azides with Alkynes Catalyzed by Cp*RuCl(COD) (2007) (0)
- Catalytic Asymmetric C—H Insertions of Rhodium(II) Azavinyl Carbenes. (2011) (0)
- Irish society of gastroenterology (1998) (0)
- A VALUABLE TOOL FOR PEPTIDE AND PROTEIN MODIFICATION (2016) (0)
- Metal-Free Carbon—Carbon Bond-Forming Processes (2012) (0)
- Oxidation of naphthene hydrocarbons in the presence of boron compounds (1978) (0)
- New reactivators of tabun-inhibited acetylcholinesterase synthesised by click chemistry (2008) (0)
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What Schools Are Affiliated With Valery V. Fokin?
Valery V. Fokin is affiliated with the following schools:
- Hong Kong University of Science and Technology
- University of Illinois Chicago
- Moscow Institute of Physics and Technology
- Technical University of Denmark
- Moscow State University
- N. I. Lobachevsky State University of Nizhny Novgorod
- University of California, Berkeley
- University of Southern California
- University of Chicago
