Direct reduction of alcohols: highly chemoselective reducing system for secondary or tertiary alcohols using chlorodiphenylsilane with a catalytic amount of indium …
M Yasuda, Y Onishi, M Ueba, T Miyai…
Index: Yasuda; Onishi; Ueba; Miyai; Baba Journal of Organic Chemistry, 2001 , vol. 66, # 23 p. 7741 - 7744
Full Text: HTML
Citation Number: 139
Abstract
The direct reduction of alcohols using chlorodiphenylsilane as a hydride source in the presence of a catalytic amount of indium trichloride is described. Benzylic alcohols, secondary alcohols, and tertiary alcohols were effectively reduced to give the corresponding alkanes in high yields. A compound bearing both primary and secondary hydroxyl groups was reduced only at the secondary site to afford the primary alcohol after workup with ...
Related Articles:
[Chen, Hao; Wang, Jianmin; Hong, Xuechuan; Zhou, Hai-Bing; Dong, Chune Canadian Journal of Chemistry, 2012 , vol. 90, # 9 p. 758 - 761]
[Alonso, Francisco; Candela, Pablo; Gomez, Cecilia; Yus, Miguel Advanced Synthesis and Catalysis, 2003 , vol. 345, # 1-2 p. 275 - 279]
[Angewandte Chemie - International Edition, , vol. 52, # 5 p. 1481 - 1485]
[ChemSusChem, , vol. 6, # 12 p. 2236 - 2239]
[Tour, James M.; Cooper, Joel P.; Pendalwar, Shekhar L. Journal of Organic Chemistry, 1990 , vol. 55, # 11 p. 3452 - 3453]