CHEMISTRY OF TAXOIDS - ONE-STEP FUNCTIONALIZATION OF THE POSITION-1, POSITION-2, POSITION-9, POSITION-10 FROM THE SELECTIVELY PROTECTED 5-O-CINNAMOYLTAXICINE-I
A. Almourabit et al., CHEMISTRY OF TAXOIDS - ONE-STEP FUNCTIONALIZATION OF THE POSITION-1, POSITION-2, POSITION-9, POSITION-10 FROM THE SELECTIVELY PROTECTED 5-O-CINNAMOYLTAXICINE-I, Tetrahedron letters, 37(51), 1996, pp. 9189-9192
A simple one-step oxidative functionalization of the positions 1, 2, 9
and 10 of 5-O-cinnamoyltaxicine I is described. The benzylidene and e
thylidene acetals were used as protective groups on the diols 1,2 and
9,10 respectively; their simultaneous direct conversion into 1-hydroxy
-2-benzoyloxy and 9-keto-10-acetoxy derivative was achieved by CrO3/Ac
OH or the Jones reagent Copyright (C) 1996 Published by Elsevier Scien
ce Ltd