A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates-Reference-Cited by-同舟云学术

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A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates

Published:2019-04 Issue:14 Volume:75 Page:2056-2061
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Foy Hayden C.,Schwan Adrian L.,Dudding Travis

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference39 articles.

1. New Paradigms for the Peroxy Acid Epoxidation of CC Double Bonds: The Role of the Peroxy Acid s-Trans Conformer and of the 1,2-H Transfer in the Epoxidation of Cyclic Allylic Alcohols

2. Mechanism of Acid-Catalyzed Epoxidation of Alkenes with Peroxy Acids

3. Advances in the Chemistry of Oxaziridines

4. Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines

5. Enantioselective synthesis of tertiary .alpha.-hydroxy carbonyl compounds using [(8,8-dichlorocamphoryl)sulfonyl]oxaziridine

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1. Carbanions and Electrophilic Aliphatic Substitution;Organic Reaction Mechanisms Series;2023-01-20

2. Reactions of Aldehydes and Ketones and Their Derivatives;Organic Reaction Mechanisms Series;2023-01-20

3. Diastereoselective Hydroxylation of N-tert-Butanesulfinyl Imines with 2-(Phenylsulfonyl)-3-phenyloxaziridine (Davis Oxaziridine);Organic Letters;2022-08-31

4. Recent Advances in the Preparations and Synthetic Applications of Oxaziridines and Diaziridines;Advanced Synthesis & Catalysis;2021-02-11

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