Convenient syntheses of (2R,3S,4R)-3-(tert-butyldimethylsilanyloxy)-2,4-dimethyl-5-oxopentanoic acid methoxymethylamide from methacrolein.: Preparation of C1-C7 and C17-C24 fragments of (+)-discodermolide
被引:19
作者:
Day, BW
论文数: 0引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USAUniv Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
Day, BW
[1
]
Kangani, CO
论文数: 0引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USAUniv Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
Kangani, CO
[1
]
Avor, KS
论文数: 0引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USAUniv Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
Avor, KS
[1
]
机构:
[1] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
Two new highly stereoselective routes to (2R,3S,4R)-3-(tert-butyldimethylsilanyloxy)-2,4-dimethyl-5-oxopentanoic acid methoxymethylamide, an important intermediate in natural product synthesis, are described. Both schemes are considerably shorter and less expensive than methods previously reported. The title compound was then converted to direct precursors of C1-C7 and C17-24 fragments of the potent microtubule stabilizer (+)-discodermolide. (C) 2002 Elsevier Science Ltd. All rights reserved.