A radical cyclization approach to the formal total syntheses of platencin
DSpace at IIT Bombay
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Title |
A radical cyclization approach to the formal total syntheses of platencin
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Creator |
PALANICHAMY, K
SUBRAHMANYAM, AV KALIAPPAN, KP |
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Subject |
ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS
FATTY-ACID BIOSYNTHESIS ACTIVATED DIMETHYL-SULFOXIDE C-ARYL GLYCOSIDES ANTIBACTERIAL PROPERTIES HYDROXYL GROUP STREPTOMYCES-PLATENSIS ENANTIOSELECTIVE ROUTE BIOLOGICAL EVALUATION ANTIBIOTIC PROPERTIES |
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Description |
Two different strategies leading to formal total syntheses of platencin are described. The first strategy involving Claisen rearrangement and radical cyclization provides a rapid access to the core structure of platencin, and also use minimum protective-group operations. The second strategy, a protecting group-free route, utilizes a 6-exo-trig radical cyclization and aldol condensation as key steps leading to the formal synthesis of platencin.
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Publisher |
ROYAL SOC CHEMISTRY
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Date |
2012-06-26T09:33:50Z
2012-06-26T09:33:50Z 2011 |
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Type |
Article
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Identifier |
ORGANIC & BIOMOLECULAR CHEMISTRY,9(22)7877-7886
1477-0520 http://dx.doi.org/10.1039/c1ob06155k http://dspace.library.iitb.ac.in/jspui/handle/100/14298 |
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Language |
English
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