Issue 48, 2022

Transition metal-free annulative vinylene transfer via the 1,3-dipolar reaction of N-ylides: access to benzo-fused indolizines

Abstract

An efficient metal-free annulative vinylene transfer protocol for the synthesis of benzo-fused indolizines via 1,3-dipolar cycloadditions of N-ylides with vinylene carbonate has been developed. Vinylene carbonate serves as an acetylene surrogate without any external oxidant involved. This transformation leads to the direct construction of versatile benzo-fused indolizine derivatives in moderate to good yields.

Graphical abstract: Transition metal-free annulative vinylene transfer via the 1,3-dipolar reaction of N-ylides: access to benzo-fused indolizines

Supplementary files

Article information

Article type
Communication
Submitted
09 Oct 2022
Accepted
16 Nov 2022
First published
16 Nov 2022

Org. Biomol. Chem., 2022,20, 9604-9608

Transition metal-free annulative vinylene transfer via the 1,3-dipolar reaction of N-ylides: access to benzo-fused indolizines

L. Zhao, W. Li, J. Liu, L. Ni, Z. Liu, H. Shen, H. Cao and X. Liu, Org. Biomol. Chem., 2022, 20, 9604 DOI: 10.1039/D2OB01846B

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