142075-86-3Relevant academic research and scientific papers
Highly Diastereoselective Hydrocyanation of β-Keto Sulfoxides: Synthesis of Enantiomerically Pure Cyanohydrin Derivatives
Ruano, Jose L. Garcia,Castro, Ana M. Martin,Rodriguez, Jesus H.
, p. 7235 - 7241 (2007/10/02)
The reactions of chiral β-keto sulfoxides, R1-CO-CHR2-SOTol (R1 = Me, n-Pr, i-Pr, t-Bu, Ph; R2 = H, Me) with Et2AlCN yield the corresponding sulfinyl cyanohydrins with high yields (85-96percent) and de (>96perce
1,3-Asymmetric Induction in the Reduction of α-Alkyl β-Ketosulfoxides with DIBAL/ZnBr2
Barros, David,Carreno, M. Carmen,Ruano, Jose L. Garcia,Maestro, M. Carmen
, p. 2733 - 2736 (2007/10/02)
The highly stereoselective reduction of chiral α-alkyl β-ketosulfoxides with DIBAL/ZnBr2 is governed by the configuration at the sulfur (1,3-induction) and not by that of the C-α (1,2-induction) as it has been previously reported.This fact considerably in
