作者:K.M. Bol、R.M.J. Liskamp
DOI:10.1016/s0040-4039(00)92397-9
日期:1991.9
A new approach to the synthesis of alkene dipeptide isosteres is reported which features the use of the [2,3]-Wittig-Still rearrangement, carried out in hexane. As an example the synthesis of the alkene dipeptide isostere of Gly-Ala as part of the tripeptide isostere Z-Phe-Gly-PSI[E-CH = CH]-(R, S)Ala-OH is described.