THERMAL CYCLIZATION OF KETENE DITHIOACETALS - A CONVENIENT SYNTHETIC ROUTE TO SUBSTITUTED 2(1H)-QUINOLINONES AND 2(1H)-PYRIDONES

被引：0
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作者：
PAK, CS
CHOI, EB
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来源：
SYNTHESIS-STUTTGART | 1992年 / 12期
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中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Acyl(arylcarbamoyl)ketene dithioacetals 2 and acyl(1 -alkenylcarbamoyl)ketene dithioacetals 5 obtained from the corresponding beta-oxo amides 1, 4 were thermally cyclized to give various 3-acyl-4-alkyl-thio-2(l H)-quinolinones 3, and 3-acyl-4-alkylthio-5-aryl-2(l H)-pyridones 6, respectively, depending on the substituent of the amide group.
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页码：1291 / 1294
页数：4
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