Visible-light-mediated regioselective ring-opening hydrogenolysis of donor–acceptor cyclopropanes with DIPEA and H<sub>2</sub>O-Reference-Cited by-同舟云学术

Visible-light-mediated regioselective ring-opening hydrogenolysis of donor–acceptor cyclopropanes with DIPEA and H₂O

Published:2022 Issue:7 Volume:9 Page:1960-1966
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Zhen¹,Wei Yin²^ORCID,Shi Min¹²^ORCID

Affiliation:

1. Key Laboratory for Advanced Materials and Institute of Fine Chemicals, School of Chemistry & Molecular Engineering, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, People's Republic of China

2. State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, University of Chinese Academy of Sciences, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Abstract

A visible-light-mediated regioselective ring-opening hydrogenolysis of donor–acceptor cyclopropanes has been developed for the rapid construction of alkylated aryl ketones in good yields with excellent functional group compatibility.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00047D

Reference46 articles.

1. Intramolecular donor–acceptor cyclopropane ring-opening cyclizations

2. Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis