Selectivity in Rh-catalysis with <i>gem</i>-difluorinated cyclopropanes-Reference-Cited by-同舟云学术

Selectivity in Rh-catalysis with gem-difluorinated cyclopropanes

Published:2024 Issue:28 Volume:60 Page:3764-3773
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zeng Yaxin¹,Jiang Zhong-Tao¹,Xia Ying¹^ORCID

Affiliation:

1. West China School of Public Health and West China Fourth Hospital, West China-PUMC C.C. Chen Institute of Health, and State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China

Abstract

This feature article summarizes our efforts towards developing Rh-catalyzed reactions of gem-difluorinated cyclopropanes, briefly discussing the design, selectivity, mechanisms and future research prospects.

Funder

National Natural Science Foundation of China

Thousand Young Talents Program of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC00793J

Reference90 articles.

1. Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes

2. Cyclopropanation Strategies in Recent Total Syntheses

3. Creating Stereocenters within Acyclic Systems by C–C Bond Cleavage of Cyclopropanes

4. Recent Advancement in Palladium-Catalyzed C–C Bond Activation of Strained Ring Systems: Three- and Four-Membered Carbocycles as Prominent C3/C4 Building Blocks

5. Bonding Properties of Cyclopropane and Their Chemical Consequences

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