[1,2] Stevens sigmatropic rearrangement of pyrrolidinium ylides—simple synthesis of 3-aryl-2-cyano-1-methylpiperidines
Author:
Funder
Warsaw University of Technology
Faculty of Chemistry
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference49 articles.
1. Generation of Ammonium Ylides from Metal Carbenoids;West,2002
2. Synthetic Reactions of M]C and M]N Bonds: Ylide Formation, Rearrangement, and 1,3-Dipolar Cycloaddition;Wang,2006
3. Recent advances in the Stevens rearrangement of ammonium ylides. Application to the synthesis of alkaloid natural products
4. Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement
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2. Nitrogen- and Sulfur-Based Stevens and Related Rearrangements;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023
3. Biocatalytic One-Carbon Ring Expansion of Aziridines to Azetidines via a Highly Enantioselective [1,2]-Stevens Rearrangement;Journal of the American Chemical Society;2022-03-08
4. Synthesis of 2‐Aryl‐ N ‐(EWG‐methyl)‐ N ‐methylpyrrolidinium Salts as Precursors of Ylides Entering the [1,2] Stevens Rearrangement;ChemistrySelect;2021-06-14
5. Molecular Rearrangement;Organic Reaction Mechanisms Series;2019-03-07
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