Dihalogenation of β-Keto Sulfides. Synthesis of α-Keto Methyl Esters and α-Keto S-Phenyl Thioesters

Autor:	Esmeralda A. Okino, Carlos R. O. Souto, Carlos C. Fortes
Rok vydání:	1991
Předmět:	chemistry.chemical_compound chemistry Organic Chemistry Acetone lipids (amino acids peptides and proteins) Methanol Sulfuryl chloride Solvolysis Medicinal chemistry
Zdroj:	Synthetic Communications. 21:2045-2052
ISSN:	1532-2432 0039-7911
DOI:	10.1080/00397919108019811
Popis:	α-Keto esters and α-Keto S-Phenyl Thioesters are synthesized from β-keto sulfides by dihalogenation with sulfuryl chloride followed by solvolysis with methanol and acetone/water respectively.
Databáze:	OpenAIRE
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