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Stereoselective synthesis of (+)-sordidin, the male-produced aggregation pheromone of the banana weevil Cosmopolites sordidus
被引:9
|作者:
Yadav, J. S.
[1
]
Reddy, K. Bhaskar
[1
]
Prasad, A. R.
[1
]
Rehman, H. Ur
[1
]
机构:
[1] Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
来源:
关键词:
banana weevil;
Jacobsen's resolution;
epoxide opening;
intramolecular acetalization;
D O I:
10.1016/j.tet.2007.12.051
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Stereoselective synthesis of (1S,3R,5R,7S)-(+)-sordidin, the natural male-produced aggregation pheromone of the banana weevil Cosmopolites sordidus (Germar) starting from 5-benzyloxy-(2E)-pentene-1-ol is described. The key transformations employed in the synthesis are Sharpless asymmetric epoxidation, Ueno - Stork cyclization, and Jacobsen kinetic resolution. (c) 2007 Published by Elsevier Ltd.
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页码:2063 / 2070
页数:8
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