Dearomative [2,3] sigmatropic rearrangement of ammonium ylides followed by 1,4-elimination to form α-(ortho-vinylphenyl)amino acid esters-Reference-Cited by-同舟云学术

Dearomative [2,3] sigmatropic rearrangement of ammonium ylides followed by 1,4-elimination to form α-(ortho-vinylphenyl)amino acid esters

Published:2018 Issue:26 Volume:16 Page:4833-4839
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Tayama Eiji¹²³⁴⁵^ORCID,Sotome Sho⁶³⁴⁵

Affiliation:

1. Department of Chemistry

2. Faculty of Science

3. Niigata University

4. Niigata

5. Japan

6. Graduate School of Science and Technology

Abstract

A base-induced dearomative [2,3] sigmatropic rearrangement followed by 1,4-elimination produced α-(ortho-vinylphenyl)amino acid esters.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01091A

Reference45 articles.

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3. Ring-Substitution, Enlargement, and Contraction by Base-Induced Rearrangements of N-Heterocyclic Ammonium Salts

4. R. Bach , S.Harthong and J.Lacour , in Comprehensive Organic Synthesis, II , ed. P. Knochel and G. A. Molander , Elsevier , 2014 , ch. 3.20, vol. 3

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