Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols

Nimisha Bania; Subhas Chandra Pan

doi:10.1039/C8OB01771A

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Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols†

Nimisha Bania

^a and Subhas Chandra Pan

*^a

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* Corresponding authors

^a Department of Chemistry, Indian Institute of Technology Guwahati, India
E-mail: span@iitg.ernet.in
Fax: +91-361-258-2349
Tel: +91-361-258-3304

Abstract

An organocatalytic asymmetric cascade Michael/hemiketalization/acyl transfer reaction between (E)-2-(2-nitrovinyl)phenols and 1,3-propanediones is disclosed. A cinchona alkaloid derived bifunctional thiourea catalyst was found to be the most effective for this reaction and provided the desired products in moderate to good yields with good to high enantioselectivities.

This article is part of the themed collections: Catalysis & biocatalysis in OBC and New Talent

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Article information

DOI: https://doi.org/10.1039/C8OB01771A
Article type: Communication
Submitted: 23 jul 2018
Accepted: 10 set 2018
First published: 10 set 2018

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Org. Biomol. Chem., 2019,17, 1718-1721

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Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols

N. Bania and S. C. Pan, Org. Biomol. Chem., 2019, 17, 1718 DOI: 10.1039/C8OB01771A

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Organic & Biomolecular Chemistry

Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols†

Abstract

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Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols

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