Issue 66, 2016, Issue in Progress

Catalytic enantioselective oxa-hetero-Diels–Alder reactions of enones with aryl trifluoromethyl ketones

Abstract

The development of oxa-hetero-Diels–Alder reactions of enones with aryl trifluoromethyl ketones to afford tetrahydropyranones bearing trifluoromethyl-substituted tetrasubstituted carbon centers is reported. The reactions were catalyzed by an amine-based catalyst system and afforded the products with er values up to 97 : 3.

Graphical abstract: Catalytic enantioselective oxa-hetero-Diels–Alder reactions of enones with aryl trifluoromethyl ketones

Supplementary files

Article information

Article type
Communication
Submitted
28 May 2016
Accepted
18 Jun 2016
First published
21 Jun 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2016,6, 61454-61457

Author version available

Catalytic enantioselective oxa-hetero-Diels–Alder reactions of enones with aryl trifluoromethyl ketones

D. Zhang and F. Tanaka, RSC Adv., 2016, 6, 61454 DOI: 10.1039/C6RA13859D

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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