Studies directed towards the total synthesis of rhizoxin: Stereoselective synthesis of C-12 to C-18 segment
摘要:
Chiral carbinol 5, made by a titanocene mediated ring opening of epoxy alcohol 11, was converted via an intramolecular radical cyclisation into a 'butanolide template' which was then transformed to the C-12 to C-18 segment 2 of rhizoxin (1).
Studies directed towards the total synthesis of rhizoxin: Stereoselective synthesis of C-12 to C-18 segment
摘要:
Chiral carbinol 5, made by a titanocene mediated ring opening of epoxy alcohol 11, was converted via an intramolecular radical cyclisation into a 'butanolide template' which was then transformed to the C-12 to C-18 segment 2 of rhizoxin (1).
Studies directed towards the total synthesis of rhizoxin: Stereoselective synthesis of C-12 to C-18 segment
作者:AV Rama Rao、Manjunath N Bhanu、GVM Sharma
DOI:10.1016/s0040-4039(00)61659-3
日期:1993.1
Chiral carbinol 5, made by a titanocene mediated ring opening of epoxy alcohol 11, was converted via an intramolecular radical cyclisation into a 'butanolide template' which was then transformed to the C-12 to C-18 segment 2 of rhizoxin (1).