期刊
JOURNAL OF HETEROCYCLIC CHEMISTRY
卷 44, 期 1, 页码 231-232出版社
HETERO CORPORATION
DOI: 10.1002/jhet.5570440138
关键词
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Reactions of primary selenoamides with dimethyl acetylenedicarboxylate afforded 2-aryl-5-methoxycarbonylmethylene-4,5-dihydro-1,3-selenazol-4-ones in moderate to high yields. Reactions of the primary selenoamides with acetylenedicarboxylic acid gave 2-aryl-5-carboxymethylene-4-ethoxy-4,5-dihydro-1,3selenazol-4-ols in moderate yields.
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