期刊
ORGANIC LETTERS
卷 2, 期 10, 页码 1481-1483出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol0058386
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资金
- NCI NIH HHS [CA-76497] Funding Source: Medline
[GRAPHICS] 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.
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