
Journal of the American Chemical Society p. 854 - 860 (1988)
Update date:2022-07-29
Topics:
Ireland
Smith
An efficient synthesis of streptolic acid, a product obtained from cleavage of the antibiotic streptolydigin, is described. The approach is based on the use of D-( plus )-glucose for the source of absolute stereochemistry, and the transfer of asymmetry is
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Doi:10.1002/hlca.200890255
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