Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Phosphorus in Organic Synthesis. XII. Amino Acids and Peptides. XXII. Reaction of Penicillin Sulfoxides with Diethyl Phosphorocyanidate (DEPC)
二宮 邦博塩入 孝之山田 俊一
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1976 年 24 巻 11 号 p. 2711-2715

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Reaction of penicillin sulfoxides with diethyl phosphorocyanidate (DEPC) was investigated. Treatment of benzylpenicillin (S)-sulfoxide methyl ester (4a) with a slight excess of DEPC in N, N-dimethylacetamide gave the 3-cephem (5a), the 2-cephem (6a). and the 3-methylenecepham (7a) in 22, 4, and 4% yields, respectively. Increase of the quantity of DEPC to a three or five fold excess increased the yield of the 3-cephem (5a). Phenoxymethylpenicillin (S)-sulfoxide methyl ester (4b) also afforded the 3-cephem (5b) and the 3-methylenecepham (7b) under analogous reaction conditions as above, while phthalimidopenicillin (R)-sulfoxide methyl ester (8) furnished the 3-cephem (9) and the isothiazolones (10 and 11).
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© The Pharmaceutical Society of Japan
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