Practical Access to Amines by Platinum-Catalyzed Reduction of Carboxamides with Hydrosilanes: Synergy of Dual Si− H Groups Leads to High Efficiency and …

…, E Tsutsumi, Y Motoyama, H Nagashima

Index: Hanada, Shiori; Tsutsumi, Emi; Motoyama, Yukihiro; Nagashima, Hideo Journal of the American Chemical Society, 2009 , vol. 131, # 41 p. 15032 - 15040

Full Text: HTML

Citation Number: 120

Abstract

The synergetic effect of two Si− H groups leads to efficient reduction of carboxamides to amines by platinum catalysts under mild conditions. The rate of the reaction is dependent on the distance of two Si− H groups; 1, 1, 3, 3-tetramethyldisiloxane (TMDS) and 1, 2-bis (dimethylsilyl) benzene are found to be an effective reducing reagent. The reduction of amides having other reducible functional groups such as NO2, CO2R, CN, C C, Cl, and ...

Related Articles:

Asymmetric Sommelet–Hauser Rearrangement of N??Benzylic Ammonium Salts

[Tayama, Eiji; Kimura, Hiroshi Angewandte Chemie - International Edition, 2007 , vol. 46, # 46 p. 8869 - 8871]

OXIMES: I. The Synthesis of some substituted 2-Oximinoacetophenones

[Norman,J.J. et al. Canadian Journal of Chemistry, 1962 , vol. 40, p. 1547 - 1553]

Kinetics of photoreduction of benzophenones by amines. Deamination and dealkylation of amines

[Cohen,S.G.; Stein,N.M. Journal of the American Chemical Society, 1971 , vol. 93, p. 6542 - 6551]

More Articles...