Mass Spectrometric Screening of Chiral Catalysts by Monitoring the Back Reaction of Quasienantiomeric Products: Palladium-Catalyzed Allylic Substitution
作者:Constanze A. Müller、Andreas Pfaltz
DOI:10.1002/anie.200705081
日期:2008.4.21
FeCl<sub>3</sub>·6H<sub>2</sub>O Catalyzed Disproportionation of Allylic Alcohols and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol
been found to be an efficient catalyst for the disproportionation of allylicalcohols, which provides a convenient method for selective transformation of allylicalcohols to alkenes and α,β-unsaturated ketones. Furthermore, this catalytic system is also effective for highly selective allylicreduction of allylicalcohols, allylic ethers, and allylic acetates with benzyl alcohol under neutral and convenient