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Substrate-Assisted Reductive Elimination Determining the Catalytic Cycle : A Theoretical Study on the Ni-Catalyzed 2,3-Disubstituted Benzofuran Synthesis via C-O Bond Activation

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/90940

Title: Substrate-Assisted Reductive Elimination Determining the Catalytic Cycle : A Theoretical Study on the Ni-Catalyzed 2,3-Disubstituted Benzofuran Synthesis via C-O Bond Activation
Authors: Miyazaki, Ray Browse this author
Iida, Kenji Browse this author
Ohno, Shohei Browse this author
Matsuzaki, Tsuyoshi Browse this author
Suzuki, Takeyuki Browse this author
Arisawa, Mitsuhiro Browse this author
Hasegawa, Jun-ya Browse this author →KAKEN DB
Issue Date: 12-Dec-2022
Publisher: American Chemical Society
Journal Title: Organometallics
Volume: 41
Issue: 23
Start Page: 3581
End Page: 3588
Publisher DOI: 10.1021/acs.organomet.2c00419
Abstract: 2,3-Disubstituted benzofurans with potential for pharmaceutical applications are effectively synthesized by Ni complexes via intramolecular C-O bond activation. The reaction pathway for the full catalytic cycle has been investigated using density functional theory (DFT) calculations. The rate-determin-ing step is the reductive elimination of the product. A key result is that coordination to an alkynyl group of another substrate co-occurs with elimination, which not only improves thermodynamic stability of the product but also determines the reaction pathway of the catalytic cycle. The reductive elimination assisted by the solvent molecules or free ligand results in an endergonic reaction. This result is related to the enhancement of reductive elimination of C-C coupling products by the addition of olefins or alkynes and can be recognized as a self-cocatalytic effect of the substrate. The result adds another viewpoint in the design of catalytic reaction systems with effective catalytic cycles.
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in [Organometallics], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/articlesonrequest/AOR-MMAKNDVMUJVZ8UDDE6CC
Type: article (author version)
URI: http://hdl.handle.net/2115/90940
Appears in Collections:触媒科学研究所 (Institute for Catalysis) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 長谷川 淳也

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