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  • Lewis base-catalyzed conjugate reduction and reductive aldol reaction of alpha,beta-unsaturated ketones using trichlorosilane.

Lewis base-catalyzed conjugate reduction and reductive aldol reaction of alpha,beta-unsaturated ketones using trichlorosilane.

Chemical communications (Cambridge, England) (2008-09-20)
Masaharu Sugiura, Norimasa Sato, Shunsuke Kotani, Makoto Nakajima
ABSTRACT

Lewis bases such as Ph3P=O and HMPA catalyze the 1,4-reduction of alpha,beta-unsaturated ketones with trichlorosilane, and because the 1,2-reduction of aldehydes scarcely proceeded under the conditions, one-pot reductive aldol reactions with aldehydes were successfully achieved; preliminary studies using a chiral Lewis base revealed a high potential for enantioselective catalysis.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Triphenylphosphine oxide, 98%
Sigma-Aldrich
Hexamethylphosphoramide, 99%
Sigma-Aldrich
Hexamethylphosphoramide, absolute, over molecular sieve (H2O ≤0.03%), ≥98.0% (GC)
Sigma-Aldrich
Hexamethylphosphoramide, purum, ≥98.0% (GC)