Issue 15, 2019

A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis

Abstract

ortho-Alkyl aromatic nitro compounds as vinylogous nucleophiles in catalytic asymmetric synthesis have rarely been reported. Herein an asymmetric vinylogous Michael addition of 5-methyl 4-nitroisoxazoles with α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal rhodium(III) complex has been developed. The corresponding adducts were obtained in good yields (80–96%) with excellent enantioselectivities (up to 97%). The reaction can be conducted on a gram scale with a low catalyst loading (0.25 mol%) without impacting its efficiency.

Graphical abstract: A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis

Supplementary files

Article information

Article type
Research Article
Submitted
22 May 2019
Accepted
20 Jun 2019
First published
20 Jun 2019

Org. Chem. Front., 2019,6, 2775-2779

A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis

S. Li, Y. Du and Q. Kang, Org. Chem. Front., 2019, 6, 2775 DOI: 10.1039/C9QO00676A

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