Bis(dialkylamino)cyanoboranes: highly efficient reagents for the Strecker-type aminative cyanation of aldehydes and ketonesElectronic supplementary information (ESI) available: detailed experimental procedures. See http://www.rsc.org/suppdata/cc/b2/b203645b/
One-stage synthesis of adamantyl-containing α-aminonitriles
作者:Yu. V. Popov、V. M. Mokhov、N. A. Tankabekyan
DOI:10.1134/s107042801308006x
日期:2013.8
Reactions of 2-adamantan-2-one, acetone cyanohydrin, and amine lead to the formation of substituted 2-amino-2-cyanoadamantanes. The reaction is of a general character as has been proved by examples on a series of ketones and amines and it proceeds through the formation from the acetone cyanohydrin and amines of 2-amino-2-cyanopropane derivatives reacting further with the carbonyl compounds.
Bis(dialkylamino)cyanoboranes: highly efficient reagents for the Strecker-type aminative cyanation of aldehydes and ketonesElectronic supplementary information (ESI) available: detailed experimental procedures. See http://www.rsc.org/suppdata/cc/b2/b203645b/
作者:Michinori Suginome、Akihiko Yamamoto、Yoshihiko Ito
DOI:10.1039/b203645b
日期:2002.6.19
α-Dialkylamino nitriles are formed in excellent yields in the reactions of bis(dialkylamino)cyanoboranes with a wide array of carbonyl compounds.