期刊
TETRAHEDRON LETTERS
卷 54, 期 41, 页码 5562-5566出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2013.07.125
关键词
Amaryllidaceous alkaloids; 7-Deoxypancratistatin; Epimer; Sharpless asymmetric dihydroxylation; Deoxygenation
资金
- CSIR, New Delhi, India
- NCL in-house projects [MLP 017226, MLP012726]
A highly stereocontrolled asymmetric total synthesis of epimer of (+)-7-deoxypancratistatin has been achieved from readily available starting materials via unified strategy employing Sharpless asymmetric dihydroxylation, ring closing metathesis, Overman rearrangement, hydrogenolysis and Bischler-Napieralski reaction in 15 purification steps with 15% overall yield. (C) 2013 Elsevier Ltd. All rights reserved.
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