N-Heterocyclic carbene-catalyzed remote enantioselective C-C bond formation via 1,6-addition with formyl enynes

N-Heterocyclic carbene-catalyzed remote enantioselective C-C bond formation via 1,6-addition with formyl enynes

N-Heterocyclic carbenes (NHCs) have emerged as powerful organocatalysts in controlling the stereoselectivities of the reaction sites that are remote from the catalyst-binding position. Meanwhile, the construction of a stereogenic center at the δ-position through NHC catalysis remains an unmet goal....

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Bibliographic Details
Main Authors: Peng, Xiaolin, Huang, Yixian, Wang, Wei, Li, Shiguang, Hao, Gefei, Ren, Shichao, Chi, Robin Yonggui
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2024
Subjects:
Chemistry
N-heterocyclic carbene
Organocatalysis
Online Access:https://hdl.handle.net/10356/174245
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Institution: Nanyang Technological University
Language: English
Description
Summary:N-Heterocyclic carbenes (NHCs) have emerged as powerful organocatalysts in controlling the stereoselectivities of the reaction sites that are remote from the catalyst-binding position. Meanwhile, the construction of a stereogenic center at the δ-position through NHC catalysis remains an unmet goal. Herein, we report the NHC-catalyzed enantioselective 1,6-conjugated addition reaction of formyl enynes with nucleophiles through an oxidative LUMO activation strategy. The reaction enables efficient chirality control at the δ-position of the formyl enyne substrates, providing access to high-value-added enantio-enriched pyrano[2,3-b]indole and pyrano[2,3-c]pyrazole derivatives. In addition, central-to-axial chirality transfer through the oxidation of our products was realized, enabling facile access to axially chiral pyrans.

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