Reagent-controlled regiodivergence in the [3,3]-sigmatropic rearrangement of N-(acyloxy)enamides-Reference-Cited by-同舟云学术

Reagent-controlled regiodivergence in the [3,3]-sigmatropic rearrangement of N-(acyloxy)enamides

Published:2019 Issue:22 Volume:6 Page:3721-3724
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Takeda Norihiko¹²³^ORCID,Arisawa Narumi¹²³,Miyamoto Misaki¹²³,Kobori Yukiko¹²³,Shinada Tetsuro⁴⁵⁶³^ORCID,Miyata Okiko¹²³⁴⁵^ORCID,Ueda Masafumi¹²³^ORCID

Affiliation:

1. Kobe Pharmaceutical University

2. Kobe 658-858

3. Japan

4. Graduate School of Science

5. Osaka City University

6. Osaka 558-8585

Abstract

A regiodivergent [3,3]-sigmatropic rearrangement of N-(acyloxy)enamides based on the N–O bond cleavage is achieved by changing reaction conditions.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C9QO01109A

Reference42 articles.

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2. Switchable divergent asymmetric synthesis via organocatalysis

3. Divergent reactions on racemic mixtures

4. M. Nógrádi , in Stereoselective Synthesis , VCH , New York , 1996

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