Corinna S. Schindler
American chemist
Corinna S. Schindler's AcademicInfluence.com Rankings
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Chemistry
Corinna S. Schindler's Degrees
- Bachelors Chemistry University of California, Berkeley
Why Is Corinna S. Schindler Influential?
(Suggest an Edit or Addition)According to Wikipedia, Corinna S. Schindler is a Professor of Chemistry at the University of Michigan. She develops catalytic reactions with environmentally benign metals such as iron, towards the synthesis of biologically active small molecules. For her research in the development of new catalysts, Schindler has been honored with several early-career researcher awards including the David and Lucile Packard Foundation Fellowship in 2016, the Alfred P. Sloan Fellowship in 2017, and being named a member of the C&EN Talented 12 in 2017. Schindler has served on the Editorial Board of Organic and Bimolecular Chemistry since 2018.
Corinna S. Schindler's Published Works
Published Works
- Photoredox Activation and Anion Binding Catalysis in the Dual Catalytic Enantioselective Synthesis of β-Amino Esters. (2014) (188)
- Iron(III)-catalysed carbonyl–olefin metathesis (2016) (138)
- Catalyst: Sustainable Catalysis (2017) (117)
- Polycyclic Aromatic Hydrocarbons via Iron(III)-Catalyzed Carbonyl-Olefin Metathesis. (2017) (85)
- A New Twist on Cooperative Catalysis (2013) (67)
- Synthesis of azetidines via visible-light-mediated intermolecular [2+2] photocycloadditions (2020) (64)
- Mechanistic Investigations of the Iron(III)-Catalyzed Carbonyl-Olefin Metathesis Reaction. (2017) (62)
- Functionalized azetidines via visible light-enabled aza Paternò-Büchi reactions (2019) (53)
- Total synthesis of marinomycins A-C and of their monomeric counterparts monomarinomycin A and iso-monomarinomycin A. (2007) (50)
- New avenues for the synthesis of ent-kaurene diterpenoids (2015) (48)
- 3-Aryl-2,5-Dihydropyrroles via Catalytic Carbonyl-Olefin Metathesis. (2018) (45)
- Catalytic Carbonyl-Olefin Metathesis of Aliphatic Ketones: Iron(III) Homo-Dimers as Lewis Acidic Superelectrophiles. (2018) (45)
- Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base. (2016) (42)
- Rapid formation of complexity in the total synthesis of natural products enabled by oxabicyclo[2.2.1]heptene building blocks. (2009) (41)
- GaCl3-Catalyzed Ring-Opening Carbonyl-Olefin Metathesis. (2018) (39)
- Facile formation of N-acyl-oxazolidinone derivatives using acid fluorides. (2010) (39)
- Lewis Acid Catalyzed Carbonyl–Olefin Metathesis (2017) (39)
- Total synthesis of marinomycins A-C. (2006) (38)
- Interrupted carbonyl-olefin metathesis via oxygen atom transfer (2018) (35)
- Discovery of Novel Synthetic Methodologies and Reagents during Natural Product Synthesis in the Post-Palytoxin Era. (2015) (33)
- Enantioselective synthesis of the core of banyaside, suomilide, and spumigin HKVV. (2008) (33)
- Visible-Light-Enabled Paternò-Büchi Reaction via Triplet Energy Transfer for the Synthesis of Oxetanes. (2020) (29)
- Beyond olefins: new metathesis directions for synthesis. (2018) (28)
- Synthesis of Microcin SF608 through nucleophilic opening of an oxabicyclo[2.2.1]heptane. (2010) (26)
- Total synthesis of nominal banyaside B: structural revision of the glycosylation site. (2010) (25)
- Recent advances in the application of ring-closing metathesis for the synthesis of unsaturated nitrogen heterocycles. (2019) (24)
- Reactivity of oximes for diverse methodologies and synthetic applications (2022) (24)
- Carbonyl-Olefin Metathesis. (2021) (21)
- Total Syntheses of Herqulines B and C. (2019) (20)
- Scalable Synthesis of Mycocyclosin. (2018) (20)
- Synthesis of azetidines by aza Paternò–Büchi reactions (2020) (18)
- Access to the aeruginosin serine protease inhibitors through the nucleophilic opening of an oxabicyclo[2.2.1]heptane: total synthesis of microcin SF608. (2014) (18)
- Nucleophilic opening of oxabicyclic ring systems. (2009) (16)
- Charting a course for chemistry (2019) (14)
- 1- and 2-Azetines via Visible Light-Mediated [2 + 2]-Cycloadditions of Alkynes and Oximes. (2021) (13)
- Catalytic, transannular carbonyl-olefin metathesis reactions† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c9sc03716k (2019) (13)
- Iron(III) Chloride Catalyzed Formation of 3,4-Dihydro-2H-pyrans from α-Alkylated 1,3-Dicarbonyls. Selective Synthesis of α- and β-Lapachone. (2016) (11)
- Superelectrophilic Fe(III)-Ion Pairs as Stronger Lewis Acid Catalysts for (E)-Selective Intermolecular Carbonyl-Olefin Metathesis. (2020) (11)
- Eight-Step Enantiodivergent Synthesis of (+)- and (-)-Lingzhiol. (2019) (11)
- Aluminum Chloride-Mediated Dieckmann Cyclization for the Synthesis of Cyclic 2-Alkyl-1,3-alkanediones: One-Step Synthesis of the Chiloglottones. (2017) (10)
- Lewis-Base-Catalyzed Reductive Aldol Reaction To Access Quaternary Carbons. (2018) (9)
- Interrupted Carbonyl‐Alkyne Metathesis (2020) (9)
- Models for Understanding Divergent Reactivity in Lewis Acid-Catalyzed Transformations of Carbonyls and Olefins (2019) (9)
- Superelectrophilic aluminium(iii)–ion pairs promote a distinct reaction path for carbonyl–olefin ring-closing metathesis (2020) (8)
- Iron(III) chloride-catalyzed synthesis of 3-carboxy-2,5-disubstituted furans from γ-alkynyl aryl- and alkylketones (2017) (8)
- Iron-Catalyzed Synthesis of Tetrahydronaphthalenes via 3,4-Dihydro-2H-pyran Intermediates. (2018) (8)
- Synthesis and biological evaluation of pharbinilic acid and derivatives as NF-κB pathway inhibitors. (2015) (8)
- Tetrahydropyridines via FeCl3-Catalyzed Carbonyl-Olefin Metathesis. (2020) (6)
- Hydrazone and Oxime Olefination via Ruthenium Alkylidenes. (2022) (6)
- Superelectrophilic Aluminum(III)-Ion Pairs Promote a Distinct Reaction Path for Carbonyl-Olefin Metathesis of Medium-Sized Rings (2019) (5)
- Design of a Two-Week Organic Chemistry Course for High School Students: “Catalysis, Solar Energy, and Green Chemical Synthesis” (2021) (5)
- Lewis acid-catalyzed carbonyl-olefin metathesis. (2019) (5)
- Functionalized Cyclopentanes via Sc(III)-Catalyzed Intramolecular Enolate Alkylation. (2018) (5)
- Carbonyl-Olefin Metathesis for the Synthesis of Cyclic Olefins. (2019) (4)
- Gibberellin JRA-003: A Selective Inhibitor of Nuclear Translocation of IKKα. (2019) (4)
- Photoredox Activation and Anion Binding Catalysis in the Dual Catalytic Enantioselective Synthesis of β‐Amino Esters. (2014) (4)
- Total Synthesis of Mycocyclosin and the Herqulines (2021) (3)
- Intramolecular, Visible-Light-Mediated Aza Paternò-Büchi Reactions of Unactivated Alkenes. (2021) (3)
- Catalytic, Transannular Carbonyl-Olefin Metathesis Reactions (2019) (3)
- Total Synthesis of (+)‐Cochlearol B by an Approach Based on a Catellani Reaction and Visible‐Light‐Enabled [2+2] Cycloaddition (2022) (3)
- Acid Chlorides as Formal Carbon Dianion Linchpin Reagents in the Aluminum Chloride-Mediated Dieckmann Cyclization of Dicarboxylic Acids. (2017) (3)
- Chiral Tetrahydropyridines via FeCl3-Catalyzed Carbonyl-Olefin Metathesis (2019) (2)
- 8-Step Enantiodivergent Synthesis of (+)- and (-)-Lingzhiol (2019) (2)
- High-Throughput Approach toward the Development of a Mizoroki-Heck Reaction to Access Tricyclic Spirolactones. (2020) (2)
- Total Synthesis of Marinomycins A‐C and of Their Monomeric Counterparts Monomarinomycin A and iso‐Monomarinomycin A. (2007) (2)
- Discovery of Novel Synthetic Methodologies and Reagents During Natural Product Synthesis in the Post-Palytoxin Era (2015) (2)
- Converting a Two-Week Chemistry Course for High School Students to a Virtual Format During COVID (2021) (2)
- Correction to "Intramolecular, Visible Light-Mediated Aza Paternò-Büchi Reactions of Unactivated Alkenes". (2022) (1)
- Origin of enantioselectivity reversal in Lewis acid-catalysed Michael additions relying on the same chiral source (2020) (1)
- Recognition of Symmetry as a Powerful Tool in Natural Product Synthesis (2021) (1)
- Visible Light-Mediated [2+2] Cycloaddition for the Synthesis of Azetidines via Energy Transfer (2018) (1)
- Facile Formation of N‐Acyl‐oxazolidinone Derivatives Using Acid Fluorides. (2011) (1)
- Photochemical Strategies Enable the Synthesis of Tunable Azetidine-Based Energetic Materials. (2022) (1)
- New strategies for the synthesis of 1- and 2-azetines and their applications as value-added building blocks. (2022) (1)
- The synthesis of herqulines B and C (2022) (0)
- Synthesis of Marinomycin A (2007) (0)
- Unprecedented Reactivity in Nucleophilic Ring Opening ofOxabicycles (2009) (0)
- Total synthesis of the banyaside aglycon (2010) (0)
- Catalytic, Interrupted Carbonyl-Olefin Metathesis for the Formation of Functionalized Cyclopentadienes (2023) (0)
- Synthesis of Nominal Banyaside B (2011) (0)
- Synthesis of Microcin SF608 (2010) (0)
- Thermodynamic vs. Kinetic Control Enables Lewis Acid-Induced Enantioselectivity Reversal Relying on the Same Chiral Source (2020) (0)
- Bioinspired Syntheses of Herqulines B and C from Cyclodipeptide Mycocyclosin (2018) (0)
- Synthetic Strategies Towards the Meroterpenoids Cochlearols A and B from Ganoderma cochlear (2022) (0)
- Rapid Formation of Complexity in the Total Synthesis of Natural Products Enabled by Oxabicyclo[2.2.1]heptene Building Blocks (2010) (0)
- Total Synthesis of Marinomycins A—C. (2007) (0)
- Total Synthesis of Cochlearol B via a Catellani- and Visible Light-Enabled [2+2]-Cycloaddition Approach (2022) (0)
- New reactivity in organic chemistry: a themed collection (2020) (0)
- Development of an In Situ Protocol for the Intramolecular Olefination of Oximes (2023) (0)
- Hydrazone and Oxime Olefination via Ruthenium Alkylidenes (2022) (0)
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