Novel methodology for the synthesis of trans-alkene dipeptide isosteres
作者:Youe Kong Shue、George M. Carrera、Michael D. Tufano、Alex M. Nadzan
DOI:10.1021/jo00006a027
日期:1991.3
Natural amino acids were converted to the corresponding allylic alcohols A, from which key precursors C were obtained via a three-step sequence [(a) Ac2O/Py or CbzOSu/Et3N/DMAP; (b) NMO/NaIO4/OsO4(cat.); (c) Ph3P = CR2CO2Bn]. The allylic alcohols D were further transformed to the desired pseudodipeptides I through the corresponding bromo derivatives E via a reductive deconjugation process.
SHUE, YOUE-KONG;CARRERA, GEORGE M. (JR);TUFANO, MICHAEL D.;NADZAN, ALEX M+, J. ORG. CHEM., 56,(1991) N, C. 2107-2111
作者:SHUE, YOUE-KONG、CARRERA, GEORGE M. (JR)、TUFANO, MICHAEL D.、NADZAN, ALEX M+
DOI:——
日期:——
SNUE, YOUE-KONG;CARRERA, GEORGE M. , JR.;NADZAN, ALEX M., TETRAHEDRON LETT., 28,(1987) N 28, 3225-3228
作者:SNUE, YOUE-KONG、CARRERA, GEORGE M. , JR.、NADZAN, ALEX M.