Tetrahedron Letters p. 491 - 494 (1996)
Update date:2022-08-03
Topics:
Dai, Jian-Ping
Sodeoka, Mikiko
Shibasaki, Masakatsu
Syntheses of the degradation product 3 of tautomycetin (1) and its diastereoisomers have been achieved. Comparison of the spectral data of these diastereoisomers with those of the degradation product of natural 1 indicates that tautomycetin has the 7R,9S,12S,13S,17S,18R stereochemistry.
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