| Literature DB >> 16805542 |
Abstract
[reaction: see text] Starting from D-xylose, enantioselective syntheses of 1 and 2, the proposed structures for radicamines A and B, were accomplished. Both (1)H and (13)C NMR spectra of 1 and 2 were identical with those of the natural products, but the optical rotation measurements identified that 1 and 2 were actually the enantiomers of the natural radicamines A and B, respectively.Entities:
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Year: 2006 PMID: 16805542 DOI: 10.1021/ol0609210
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005