Journal of the American Chemical Society p. 4957 - 4964 (1986)
Update date:2022-07-31
Topics:
Cane, David E.
Liang, Tzyy-Chyau
Taylor, Paul B.
Chang, Conway
Yang, Chi-Ching
The stereochemical course of the chain-elongation steps of the biosynthesis of the macrolide antibiotic erythromycin has been investigated.Incorporation of <2-(2)H2,2-(13)C>propionate into erythromycins A and B by cultures of Streptomyces erythreus was fo
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(2004)Doi:10.1021/ja801925q
(2008)Doi:10.1016/S0022-328X(00)81003-7
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(1995)Doi:10.1135/cccc19811607
(1981)
