Chemical Synthesis and Structural Study of Lincomycin Sulfoxides and a Sulfone
Oxidation of lincomycin with dimethyldioxirane resulted in the sulfoxide-glycosides 3a and 3b, whose treatment with osmium tetraoxide and N-methylmorpholine-N-oxide afforded the same sulfone; 4. According to FAB-MS and CD investigations, the absolute configuration of the sulfur atom in 3a and 3b is...
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Published in | Journal of antibiotics Vol. 50; no. 10; pp. 866 - 873 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
TOKYO
JAPAN ANTIBIOTICS RESEARCH ASSOCIATION
1997
Japan Antibiotics Research Assoc Japan Antibiotics Research Association |
Subjects | |
Online Access | Get full text |
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Summary: | Oxidation of lincomycin with dimethyldioxirane resulted in the sulfoxide-glycosides 3a and 3b, whose treatment with osmium tetraoxide and N-methylmorpholine-N-oxide afforded the same sulfone; 4. According to FAB-MS and CD investigations, the absolute configuration of the sulfur atom in 3a and 3b is R and S, respectively. The new, unsaturated antibiotic analog (6) derived from clindamycin exists in the 4C1 conformation. The antibiotic activities of the synthesized compounds were also studied. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0021-8820 1881-1469 |
DOI: | 10.7164/antibiotics.50.866 |