Issue 71, 2018

Pd-catalyzed [3 + 2] cycloaddition of vinylcyclopropanes with 1-azadienes: synthesis of 4-cyclopentylbenzo[e][1,2,3]oxathiazine 2,2-dioxides

Abstract

The palladium-catalyzed [3 + 2] cycloaddition of vinylcyclopropanes and 1-azadienes has been developed under mild reaction conditions, giving the multisubstituted cyclopentane derivatives in good to excellent yields with moderate to good diastereoselectivities. The relative configuration of both diastereomers of the products have been determined through X-ray crystallographic diffraction.

Graphical abstract: Pd-catalyzed [3 + 2] cycloaddition of vinylcyclopropanes with 1-azadienes: synthesis of 4-cyclopentylbenzo[e][1,2,3]oxathiazine 2,2-dioxides

Supplementary files

Article information

Article type
Paper
Submitted
26 Oct 2018
Accepted
29 Nov 2018
First published
05 Dec 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 40798-40803

Pd-catalyzed [3 + 2] cycloaddition of vinylcyclopropanes with 1-azadienes: synthesis of 4-cyclopentylbenzo[e][1,2,3]oxathiazine 2,2-dioxides

Y. Lin, Q. Wang, Y. Wu, C. Wang, H. Jia, C. Zhang, J. Huang and H. Guo, RSC Adv., 2018, 8, 40798 DOI: 10.1039/C8RA08881K

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