| Literature DB >> 10814478 |
Abstract
[reaction--see text] Each of four diastereomers of structure 2, corresponding to the lipophilic side chain of scyphostatin (1), were prepared. Careful analysis of their NMR spectral data and comparison with those of the natural product corroborates the recently reported (Org. Lett. 2000, 2, 505) stereochemical assignment. A strategy for the stereoselective synthesis of 2 has been achieved.Entities:
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Year: 2000 PMID: 10814478 DOI: 10.1021/ol0058386
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005