| Literature DB >> 22545759 |
Maria Matveenko1, Guangxin Liang, Erica M W Lauterwasser, Eva Zubía, Dirk Trauner.
Abstract
A concise asymmetric approach to the indeno-tetrahydropyridine core of the unusual alkaloid haouamine B allowed for an investigation of a biomimetic oxidative phenol coupling as a proposed biosynthetic step, and ultimately provided access to the published structure of the natural product. As a consequence of our synthetic studies, the structure of haouamine B has been revised.Entities:
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Year: 2012 PMID： 22545759 DOI： 10.1021/ja301326k
Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419