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Diaryldiazoketones as Effective Carbene Sources for Highly Selective Rh(II)-Catalyzed Intermolecular C-H Functionalization.

ABSTRACT: A novel donor/acceptor carbene intermediate has been developed using diaryldiazoketones as carbene precursors. In the presence of the chiral dirhodium catalyst, Rh₂(S-TPPTTL)₄, diaryldiazoketones undergo highly regio-, stereo-, and diastereoselective C-H functionalization of activated and unactivated secondary and tertiary C-H bonds. Computational studies revealed that the arylketo group behaves differently than the carboxylate acceptor group because the orientation of the arylketo group predetermines which face of the carbene will be attacked.

SUBMITTER: Nguyen TH

PROVIDER: S-EPMC10979447 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Diaryldiazoketones as Effective Carbene Sources for Highly Selective Rh(II)-Catalyzed Intermolecular C-H Functionalization.

Nguyen Terrence-Thang H TH Bosse Aaron T AT Ly Duc D Suarez Camila A CA Fu Jiantao J Shimabukuro Kristin K Musaev Djamaladdin G DG Davies Huw M L HML

Journal of the American Chemical Society 20240313 12

A novel donor/acceptor carbene intermediate has been developed using diaryldiazoketones as carbene precursors. In the presence of the chiral dirhodium catalyst, Rh2(S-TPPTTL)4, diaryldiazoketones undergo highly regio-, stereo-, and diastereoselective C-H functionalization of activated and unactivated secondary and tertiary C-H bonds. Computational studies revealed that the arylketo group behaves differently than the carboxylate acceptor group because the orientation ...[more]

PMID: 38478893

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