Issue 100, 2024

Atroposelective synthesis of axially chiral indolizinylpyrroles by catalytic asymmetric Paal–Knorr reaction

Abstract

We present herein a highly efficient atroposelective synthesis of five/five-membered N-indolizinylpyrrole through the chiral phosphoric acid (CPA) catalyzed Paal–Knorr reaction of 3-aminoindolizines and 1,4-diketones. The reaction features mild reaction conditions, broad substrate scope and excellent enantioselectivity. Moreover, this method provides a facile approach to a novel axially chiral indolizine-pyrrole framework.

Graphical abstract: Atroposelective synthesis of axially chiral indolizinylpyrroles by catalytic asymmetric Paal–Knorr reaction

Supplementary files

Article information

Article type
Communication
Submitted
10 Sep 2024
Accepted
15 Nov 2024
First published
20 Nov 2024

Chem. Commun., 2024,60, 14984-14987

Atroposelective synthesis of axially chiral indolizinylpyrroles by catalytic asymmetric Paal–Knorr reaction

W. Zhan, J. Hu, X. Chen, G. Luo and X. Song, Chem. Commun., 2024, 60, 14984 DOI: 10.1039/D4CC04678A

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