Issue 20, 2019

Asymmetric synthesis of multifunctional aryl allyl ethers by nucleophilic catalysis

Abstract

Asymmetric allylic substitution of Morita–Baylis–Hillman (MBH) carbonates with less-nucleophilic phenols mediated by nucleophilic amine catalysis was successfully developed. A variety of substituted aryl allyl ethers were afforded with moderate to high yields with excellent enantioselectivities. The chiral MBH alcohol could be easily accessed from the corresponding aryl allyl ether.

Graphical abstract: Asymmetric synthesis of multifunctional aryl allyl ethers by nucleophilic catalysis

Supplementary files

Article information

Article type
Paper
Submitted
08 Jan 2019
Accepted
02 Apr 2019
First published
12 Apr 2019
This article is Open Access
Creative Commons BY license

RSC Adv., 2019,9, 11585-11588

Asymmetric synthesis of multifunctional aryl allyl ethers by nucleophilic catalysis

S. Zhao, L. Jin, Z. Chen, X. Rui, J. He, R. Xia, K. Chen, X. Chen, Z. Yin and X. Chen, RSC Adv., 2019, 9, 11585 DOI: 10.1039/C9RA00155G

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.

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