Elucidating the selectivity of dyotropic rearrangements of β-lactones: a computational survey-Reference-Cited by-同舟云学术

Elucidating the selectivity of dyotropic rearrangements of β-lactones: a computational survey

Published:2022 Issue:2 Volume:9 Page:329-341
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhang Jingyang¹,Ma Yumiao²,Qiu Ke¹,Li Bo³,Xue Zhengwen¹,Tian Boxue¹^ORCID,Tang Yefeng¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Tsinghua University, Beijing 100084, China

2. BSJ Institute, Beijing, 100084, China

3. Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California, 91125, USA

Abstract

A comprehensive computational study on dyotropic rearrangements of β-lactones has been performed for the first time, which provides a valuable guidance for predicting and controlling the selectivity of the reactions.

Funder

Natural Science Foundation of Beijing Municipality

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D1QO01591E

Reference54 articles.

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