Multitasking rhodium-catalyzed remote C(sp<sup>3</sup>)–H functionalization reactions of acyclic dienes to yield benzene-fused heterocycles

Remote C(sp 3 )–H bond functionalization reactions are environmentally benign methods for not only acyclic molecules but also cyclic molecules, 2,3-disubstituted dihydrobenzofurans.

Authors

Mitsuhiro Arisawa (ORCID: https://orcid.org/0000-0002-7937-670X)
Makoto Sako (ORCID: https://orcid.org/0000-0002-4268-7002)
Y. SATO (ORCID: https://orcid.org/0000-0002-7377-1872)
Tsuyoshi Matsuzaki
Masaharu Takatsuki
Takeyuki Suzuki (ORCID: https://orcid.org/0000-0002-2137-0276)
Momoko Nagafuchi

Institutions

The University of Osaka (JP)

Publication Details

Journal: Green Chemistry
Published: 2024-11-08
DOI: https://doi.org/10.1039/d4gc04927f
Citations: 2
Primary Topic: Catalytic C–H Functionalization Methods
Type: article
Field-Weighted Citation Impact: 0.50

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article

Multitasking rhodium-catalyzed remote C(sp³)–H functionalization reactions of acyclic dienes to yield benzene-fused heterocycles

Mitsuhiro Arisawa, Makoto Sako, Y. SATO, Tsuyoshi Matsuzaki et al.

Nov 8, 2024

2 citations

Green Chemistry

Catalytic C–H Functionalization Methods

0.50

article

Multitasking rhodium-catalyzed remote C(sp³)–H functionalization reactions of acyclic dienes to yield benzene-fused heterocycles

Mitsuhiro Arisawa, Makoto Sako, Y. SATO, Tsuyoshi Matsuzaki, Masaharu Takatsuki, Takeyuki Suzuki, Momoko Nagafuchi

November 8, 2024article en

2 citations

Abstract

Remote C(sp 3 )–H bond functionalization reactions are environmentally benign methods for not only acyclic molecules but also cyclic molecules, 2,3-disubstituted dihydrobenzofurans.

Green ChemistryVol. 27(1)

The University of Osaka (JP)

Openalex Percentile: Top 38%

Catalytic C–H Functionalization Methods

0.50

DOI Source OpenAlex

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