Issue 9, 2010

Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst

Abstract

Efficient kinetic resolution of racemic 3-nitro-2H-chromenes by bifunctional thiourea afforded optically active (R)-3-nitro-2H-chromene derivatives with moderate to good enantioselectivities, which simultaneously gave the multifunctional 3,4-diphenyl-3a-nitrobenzopyrano-[3,4-c]-pyrrolidine-1,1-dicarboxylate derivatives with four vicinal chiral carbon centers.

Graphical abstract: Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst

Supplementary files

Article information

Article type
Paper
Submitted
29 Oct 2009
Accepted
22 Feb 2010
First published
11 Mar 2010

Org. Biomol. Chem., 2010,8, 2117-2122

Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst

J. Xie, L. Fan, H. Su, X. Li and D. Xu, Org. Biomol. Chem., 2010, 8, 2117 DOI: 10.1039/B922668K

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