期刊
TETRAHEDRON LETTERS
卷 50, 期 31, 页码 4506-4508出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.05.069
关键词
Indole; Alkaloid; Tetrahydro-beta-carboline; Spectroscopy; Asymmetric total synthesis
资金
- Japan Society for the Promotion of Science
Eudistomidin B, isolated from a marine tunicate, was originally assigned a tetrahydro-p-carboline structure with a 2-p-tolylethanamine residue. Asymmetric total synthesis of the reported structure of natural product, which features an intramolecular diastereoselective Pictet-Spengler cyclization, suggests that the reported structure of the natural product needs to be revised. (C) 2009 Elsevier Ltd. All rights reserved.
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