期刊
TETRAHEDRON-ASYMMETRY
卷 23, 期 8, 页码 587-593出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2012.04.004
关键词
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资金
- DST, New Delhi, India [SR/S1/OC-08/2011]
- UGC (New Delhi)
An efficient enantioselective synthesis of the potent anticancer agent (+)-duryne was achieved by the use of a one-pot organocatalyzed hydroxylation/Ohira-Bestmann and Grubbs cross-metathesis/selective cis-Wittig reaction. This new approach is envisioned to facilitate the synthesis of every representative member of the family. (C) 2012 Elsevier Ltd. All rights reserved.
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