Issue 112, 2015

Palladium-catalyzed asymmetric [3+2] cycloaddition to construct 1,3-indandione and oxindole-fused spiropyrazolidine scaffolds

Abstract

Palladium-catalyzed asymmetric [3+2] cycloaddition of 3-diazooxindoles with 2-vinylspiro[cyclopropane-1,2′-indene]-1′,3′-dione proceeded smoothly in the presence of chiral imidazoline–phosphine ligands to give the corresponding highly functionalized spiropyrazolidine derivatives in good to excellent yields (52–99%) along with good enantioselectivities (48–82% ee) under mild conditions.

Graphical abstract: Palladium-catalyzed asymmetric [3+2] cycloaddition to construct 1,3-indandione and oxindole-fused spiropyrazolidine scaffolds

Supplementary files

Article information

Article type
Paper
Submitted
25 Sep 2015
Accepted
20 Oct 2015
First published
21 Oct 2015

RSC Adv., 2015,5, 92545-92548

Author version available

Palladium-catalyzed asymmetric [3+2] cycloaddition to construct 1,3-indandione and oxindole-fused spiropyrazolidine scaffolds

B. Cao, L. Mei, X. Li and M. Shi, RSC Adv., 2015, 5, 92545 DOI: 10.1039/C5RA19838K

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