Dramatic Effects of Halogen Substitution and Solvent on the Rates and Mechanisms of Nucleophilic Substitution Reactions of Aziridines
Author:
Affiliation:
1. U.S. Army Edgewood Chemical Biological Center, APG, Maryland 21010-5424
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo7023224
Reference51 articles.
1. De Novo Synthesis of Tamiflu via a Catalytic Asymmetric Ring-Opening of meso-Aziridines with TMSN3
2. Synthesis of 1-Arylmethyl-2-(2-cyanoethyl)aziridines and Their Rearrangement into Novel 2-(Aminomethyl)cyclopropanecarbonitriles
3. Silylmethyl-Substituted Aziridine and Azetidine as Masked 1,3- and 1,4-Dipoles for Formal [3 + 2] and [4 + 2] Cycloaddition Reactions
4. Ring Opening and Expansion of Aziridines in a Silica−Water Reaction Medium
5. Synthesis of 1-Arylmethyl-2-(cyanomethyl)aziridines and Their Ring Transformation into Methyl N-(2-Cyanocyclopropyl)benzimidates
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