Photoredox-catalyzed, oxygen-directed unactivated δ-C(sp<sup>3</sup>)–H functionalization toward oxepanes-Reference-Cited by-同舟云学术

Photoredox-catalyzed, oxygen-directed unactivated δ-C(sp³)–H functionalization toward oxepanes

Published:2023 Issue:15 Volume:10 Page:3870-3874
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wu Hao¹,He Shi-Hui¹,Qin Hai-Tao¹,Liu Feng¹²^ORCID

Affiliation:

1. Jiangsu Key Laboratory of Neuropsychiatric Diseases and Department of Medicinal Chemistry, College of Pharmaceutical Sciences, Soochow University, 199 Ren-Ai Road, Suzhou, Jiangsu 215123, People's Republic of China

2. Jiangsu Province Engineering Research Center of Precision Diagnostics and Therapeutics Development, College of Pharmaceutical Sciences, Soochow University, 199 Ren-Ai Road, Suzhou, Jiangsu 215123, People's Republic of China

Abstract

A concise photoredox-catalyzed [5 + 2] annulation reaction is developed for the synthesis of alkene/alkyne-containing oxepanes.

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00689A

Reference31 articles.