Issue 7, 2021

N-Heterocyclic carbene catalyzed asymmetric [3 + 3] cycloaddtion of β,β-disubstituted, α,β-unsaturated carboxylic esters with 3-aminobenzofurans

Abstract

An N-heterocyclic carbene (NHC) catalyzed formal [3 + 3] cycloaddition reaction of β,β-disubstituted, α,β-unsaturated carboxylic esters with 3-aminobenzofurans is doucumented, furnishing benzofuran fused δ-lactams bearing an all-carbon quaternary stereocenter with moderate to excellent yields and excellent enantioselectivies. Further gram-scale preparation and synthetic transformation of the cycloadducts demonstrate good practicality and applicability of this β-carbon functionalization reaction.

Graphical abstract: N-Heterocyclic carbene catalyzed asymmetric [3 + 3] cycloaddtion of β,β-disubstituted, α,β-unsaturated carboxylic esters with 3-aminobenzofurans

Supplementary files

Article information

Article type
Research Article
Submitted
27 Nov 2020
Accepted
06 Feb 2021
First published
08 Feb 2021

Org. Chem. Front., 2021,8, 1569-1574

N-Heterocyclic carbene catalyzed asymmetric [3 + 3] cycloaddtion of β,β-disubstituted, α,β-unsaturated carboxylic esters with 3-aminobenzofurans

C. He, Y. Zhou, Z. Li, J. Xu and X. Chen, Org. Chem. Front., 2021, 8, 1569 DOI: 10.1039/D0QO01489C

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