Aryne triggered [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers-Reference-Cited by-同舟云学术

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Aryne triggered [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers

Published:2017 Issue:23 Volume:15 Page:4946-4950
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Tan Jiajing¹²³⁴⁵^ORCID,Zheng Tianyu¹²³⁴⁵,Xu Kun⁶⁷⁸⁹,Liu Changyao¹⁰¹¹¹²¹³

Affiliation:

1. Department of Organic Chemistry

2. Faculty of Science

3. Beijing University of Chemical Technology

4. Beijing 100029

5. China

6. College of Chemistry and Pharmaceutical Engineering

7. Nanyang Normal University

8. Nanyang

9. P. R. China

10. School of Food and Chemical Engineering

11. Beijing Technology and Business University

12. Beijing

13. People's Republic of China

Abstract

An efficient protocol for [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers is reported.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00914C

Reference71 articles.

1. [2,3]-Wittig sigmatropic rearrangements in organic synthesis

2. Acyclic Stereocontrol via [2,3]-Wittig Sigmatropic Rearrangement

3. Investigations of the [2,3]-Sigmatropic Rearrangements of Vinylaziridines and Allylic Amines

4. Sigmatropic rearrangements of ‘onium’ ylids

5. Intramolecular generation and rearrangement of oxonium ylides: methodology studies and their application in synthesis

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