Journal article

Publication year: 2011

Pages: 1262-1264

Journal: Accounts and Rapid Communications in Chemical Synthesis

Volume number: 2011

Issue number: 9

DOI Link: https://doi.org/10.1055/s-0030-1259956

Publisher: Thieme

Abstract: 

A bifunctional thiourea-catalyzed tandem approach of oxa-Michael-aza-Henry-desulfonamidation
was used to synthesize chiral 2-aryl-3-nitro-2H-chromenes.
This method provides direct access to the corresponding products
in moderate to good yields and enantioselectivities.

Harvard Citation style: Zhang, Z., Jakab, G. and Schreiner, P. (2011) Enantioselective Synthesis of 2-Aryl-3-nitro-2H-chromenes Catalyzed by a Bifunctional Thiourea, Accounts and Rapid Communications in Chemical Synthesis, 2011(9), pp. 1262-1264. https://doi.org/10.1055/s-0030-1259956

APA Citation style: Zhang, Z., Jakab, G., & Schreiner, P. (2011). Enantioselective Synthesis of 2-Aryl-3-nitro-2H-chromenes Catalyzed by a Bifunctional Thiourea. Accounts and Rapid Communications in Chemical Synthesis. 2011(9), 1262-1264. https://doi.org/10.1055/s-0030-1259956