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Synthesis of cladobotryal, CJ16,169, and CJ16,170
Journal article   Peer reviewed

Synthesis of cladobotryal, CJ16,169, and CJ16,170

Barry B Snider and Qinglin Che
Organic Letters, Vol.6(17), pp.2877-2880
08/01/2004
PMID: 15330637

Abstract

Lactones - chemical synthesis Cyclization Oxidation-Reduction Furans - chemistry Molecular Structure Furans - chemical synthesis Pyridones - chemistry Pyridones - chemical synthesis
Condensation of hydroxypyridone 7 with ethyl pyruvate and p-chlorothiophenol, reduction, and cyclization afforded 77% of lactone 6. Protection of the pyridone, acylation of the enolate with tigloyl chloride, and deprotection provided keto lactone 22. Reduction and dehydrative cyclization completed short and efficient syntheses of 2 and 3.

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