Journalartikel

Jahr der Veröffentlichung: 2011

Seiten: 1262-1264

Zeitschrift: Accounts and Rapid Communications in Chemical Synthesis

Bandnummer: 2011

Heftnummer: 9

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

Verlag: 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-Zitierstil: 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-Zitierstil: 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