Decarbonylative cycloaddition of 1<i>H</i>-indene-1,2,3-trione and norbornene <i>via</i> rhodium(<scp>i</scp>)-catalyzed carbon–carbon bond cleavage-Reference-Cited by-同舟云学术

Decarbonylative cycloaddition of 1H-indene-1,2,3-trione and norbornene via rhodium(i)-catalyzed carbon–carbon bond cleavage

Published:2022 Issue:23 Volume:46 Page:11108-11117
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Hu Zhenzhu¹^ORCID,Wang Yuhang¹^ORCID,Ma Peng¹^ORCID,Wang Jianhui¹²,Liu Guiyan³^ORCID

Affiliation:

1. Department of Chemistry, College of Science, Tianjin University, Tianjin, 300350, P. R. China

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), 30072, P. R. China

3. Tianjin Key Laboratory of Structure and Performance for Functional Molecules; Key Laboratory of Inorganic–Organic hybrid Functional Material Chemistry; College of Chemistry, Tianjin Normal University, Tianjin, 300387, P. R. China

Abstract

2,3-Dihydro-1H-inden-1-one derivatives were synthesized by a [5+2−2] decarbonylative cycloaddition of 1H-indene-1,2,3-trione and norbornene via rhodium(i) catalyzed direct carbon–carbon bond cleavage.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Tianjin City

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ01708C

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