Oxidation of Aliphatic α,β-Unsaturated Aldimines to Amides Specifically by Oxone with AlCl3
摘要:
alpha,beta-Unsaturated aldimines were specifically oxidized to amides with Oxone in the presence of AlCl3 as a Lewis acid in CH2Cl2. No migration of aryl group occurred in the rearrangement reaction.
Danks, Timothy N.; Thomas, Susan E., Journal of the Chemical Society. Perkin transactions I, 1990, # 3, p. 761 - 765
作者:Danks, Timothy N.、Thomas, Susan E.
DOI:——
日期:——
The first example of asymmetric induction in an anionic amino-Cope rearrangement
作者:Steven M. Allin、Martin A.C. Button
DOI:10.1016/s0040-4039(98)00487-0
日期:1998.5
The anionic amino-Cope rearrangement of suitably functionalized acyclic 3-amino-1,5-diene substrates has been achieved and we report the first example of an asymmetric anionic amino-Cope rearrangement to yield an enantiomerically enriched product (75% e.e.). The absolute stereochemistry of the products has been verified and transition state models are proposed to rationalize the stereochemical outcome
Oxidation of Aliphatic <font>α,β</font>-Unsaturated Aldimines to Amides Specifically by Oxone with AlCl<sub>3</sub>
作者:Zhou Lu、Lijun Peng、Wentao Wu、Longmin Wu
DOI:10.1080/00397910802138892
日期:2008.6.27
alpha,beta-Unsaturated aldimines were specifically oxidized to amides with Oxone in the presence of AlCl3 as a Lewis acid in CH2Cl2. No migration of aryl group occurred in the rearrangement reaction.