Issue 11, 2017, Issue in Progress

Organocatalytic asymmetric conjugate addition of t-butyl nitroacetate to o-quinone methides: synthesis of optically active α-nitro-β,β-diaryl-propionates

Abstract

An asymmetric conjugate addition of t-butyl nitroacetate to in situ generated o-quinone methides had been developed. A chiral squamide derived from 9-amino-9-deoxyepiquinine was found to be the efficient catalyst. α-Nitro-β,β-diaryl-propionates could be obtained in good yields and with excellent enantioselectivities.

Graphical abstract: Organocatalytic asymmetric conjugate addition of t-butyl nitroacetate to o-quinone methides: synthesis of optically active α-nitro-β,β-diaryl-propionates

Supplementary files

Article information

Article type
Paper
Submitted
12 Dec 2016
Accepted
11 Jan 2017
First published
20 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 6660-6663

Organocatalytic asymmetric conjugate addition of t-butyl nitroacetate to o-quinone methides: synthesis of optically active α-nitro-β,β-diaryl-propionates

R. Liu, X. Tang, X. Zhang, M. Yan and A. S. C. Chan, RSC Adv., 2017, 7, 6660 DOI: 10.1039/C6RA28068D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements