A Rapid Approach to Amino-Acid Derivatives by [2,3]-Stevens Rearrangement
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2000-6494.pdf
Cited by 40 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis of 2‐Aryl‐ N ‐(EWG‐methyl)‐ N ‐methylpyrrolidinium Salts as Precursors of Ylides Entering the [1,2] Stevens Rearrangement;ChemistrySelect;2021-06-14
2. Chiral N,N′-dioxide/Mg(OTf)2 complex-catalyzed asymmetric [2,3]-rearrangement of in situ generated ammonium salts;Chemical Science;2020
3. Asymmetric Synthesis of Cα‐Substituted Prolines through Curtin–Hammett‐Controlled Diastereoselective N‐Alkylation;Chemistry – A European Journal;2019-01-21
4. Asymmetric Cα-Alkylation of Proline via Chirality Transfers of Conformationally Restricted Proline Derivative: Application to the Total Synthesis of (−)-Amathaspiramide F;Organic Letters;2018-09-20
5. Isothiourea-catalysed chemo- and enantioselective [2,3]-sigmatropic rearrangements of N,N-diallyl allylic ammonium ylides;Tetrahedron;2017-07
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