Tambor; Gubler, Helvetica Chimica Acta, 1919, vol. 2, p. 107
作者:Tambor、Gubler
DOI:——
日期:——
An expedient synthesis of enantioenriched substituted (2-benzofuryl)arylcarbinols via tandem Rap–Stoermer and asymmetric transfer hydrogenation reactions
An expedientsynthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap–Stoermer reaction/catalytic asymmetric transfer hydrogenation (ATH) using substituted salicylaldehyde and α-haloaryl, heteroaryl ketones.