Enantioselective hydrogenation of α-ketoamides over Pt/A12O3 modified by cinchona alkaloids
Pyruvamide and its N-alkylated derivatives have been synthesised and hydrogenated enantioselectively to the corresponding alcohols over an alumina-supported Pt catalyst chirally modified by adsorbed cinchonidine. Depending on the substrate structure and r
Wang,Mallat,Baiker
p. 2133 - 2140
(2007/10/03)
Tin(II) Amides: New Reagents for the Conversion of Esters to Amides
Mixed tin(II) amides are generated, in situ, via addition of aliphatic amines to Sn2.Condensation of these reagents with esters yields amides.
Wang, Wei-Bo,Roskamp, Eric J.
p. 6101 - 6103
(2007/10/02)
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