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Theoretical study on the mechanism, chemo- and enantioselectivity of the Ag- vs. Rh-catalyzed intramolecular carbene transfer reaction of diazoacetamides.


ABSTRACT: To explore the mechanism of silver and rhodium catalysis and reveal the origin of the chemo- and enantioselectivity of the reaction, density functional theory calculations were performed on the first silver-catalyzed highly enantioselective carbene transfer reaction. The calculation results reveal that when silver is used as a catalyst, due to the participation of the phosphate anion in the transition state, the enhanced nucleophilicity of the α-diazoacetamide unit promotes smooth dearomatization before generation of the silver carbene. Because the generated rhodium carbene has stronger electrophilicity, typical carbene reactions (C-H insertion and the Büchner reaction) are favored. In addition, in the process of silver catalyzed dearomatization, the formation of an R-type transition state is determined by the small torsion energy and strong interaction energy.

SUBMITTER: Song Q 

PROVIDER: S-EPMC9214843 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Theoretical study on the mechanism, chemo- and enantioselectivity of the Ag- <i>vs.</i> Rh-catalyzed intramolecular carbene transfer reaction of diazoacetamides.

Song Qingmin Q   Wu Jiayi J   Tzoukras Nikolaos V NV   Wu Yong Y   Nolan Steven P SP  

RSC advances 20220622 28


To explore the mechanism of silver and rhodium catalysis and reveal the origin of the chemo- and enantioselectivity of the reaction, density functional theory calculations were performed on the first silver-catalyzed highly enantioselective carbene transfer reaction. The calculation results reveal that when silver is used as a catalyst, due to the participation of the phosphate anion in the transition state, the enhanced nucleophilicity of the α-diazoacetamide unit promotes smooth dearomatizatio  ...[more]

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