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An Efficient Synthesis of [1,2,4]Triazolo[3,2-d][1,5]benzoxazepin-2-thiones, a Kind of Novel Tricyclic O,N-Heterocycles

An Efficient Synthesis of [1,2,4]Triazolo[3,2-d][1,5]benzoxazepin-2-thiones, a Kind of Novel Tricyclic O,N-Heterocycles
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摘要 A series of novel tricyclic O,N-heterocycles, [1,2,4]triazolo[3,2-d][1,5]benzoxazepin-2-thiones 7 were achieved via acid-induced ring closure of the geminal arylazo isothiocyanate compounds 5 which were derived from substituted chroman-4-ones, followed by feasible ring expansion with simultaneous insertion of the nitrogen atom into the carbon skeleton. The X-ray crystal structure of 7d was also described. A series of novel tricyclic O,N-heterocycles, [1,2,4]triazolo[3,2-d][1,5]benzoxazepin-2-thiones 7 were achieved via acid-induced ring closure of the geminal arylazo isothiocyanate compounds 5 which were derived from substituted chroman-4-ones, followed by feasible ring expansion with simultaneous insertion of the nitrogen atom into the carbon skeleton. The X-ray crystal structure of 7d was also described.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2004年第3期290-295,共6页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation of China (No. 20372015) and the Key Organic Synthesis Laboratory of Jiangsu Province (No. KJS01016).
关键词 geminal arylazo isothiocyanate ring closure REARRANGEMENT [1 2 4]triazolo[3 2-d][1 5]benzoxazepin-2-thiones geminal arylazo isothiocyanate, ring closure, rearrangement, [1,2,4]triazolo[3,2-d][1,5]benzoxazepin-2-thiones
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