Trichlorosilane-imine complexes. A new method for the reduction of imines to amines
RA Benkeser, DC Snyder
Index: Benkeser, Robert A.; Snyder, Dudley C. Journal of Organometallic Chemistry, 1982 , vol. 225, # 1 p. 107 - 115
Full Text: HTML
Citation Number: 31
Abstract
Abstract It has been found that trichlorosilane adds regio-specifically to the carbon—nitrogen double bond of imines under mild conditions to yield hydrolytically unstableN-trichlorosilyl intermediates. The latter can be hydrolyzed in situ by alcoholic base to give the corresponding amines in moderate to good yields. Variously substituted aldo and keto imines, both alkyl and aryl, were tested to demonstrate the scope of the reaction. The ...
Related Articles:
[Giannoccaro, Potenzo; Nobile, Cosimo Francesco; Mastrorilli, Pietro; Ravasio, Nicoletta Journal of Organometallic Chemistry, 1991 , vol. 419, # 1 p. 251 - 258]
[Khatri, Praveen K.; Jain, Suman L.; Sivakumar K.; Sain, Bir Organic and Biomolecular Chemistry, 2011 , vol. 9, # 9 p. 3370 - 3374]
[Huang, Jing-Mei; Zhang, Jue-Fei; Dong, Yi; Gong, Wen Journal of Organic Chemistry, 2011 , vol. 76, # 9 p. 3511 - 3514]
[Fiz; Usero; Casado International Journal of Chemical Kinetics, 1993 , vol. 25, # 5 p. 341 - 351]
[Bailey,P.S. et al. Journal of Organic Chemistry, 1968 , vol. 33, p. 2675 - 2680]