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A practical synthesis of 2,3-dihydro-1,5-benzothiazepines
Green Chemistry ( IF 9.3 ) Pub Date : 2017-10-30 00:00:00 , DOI: 10.1039/c7gc02097j
Domenico C. M. Albanese 1, 2, 3, 4 , Nicoletta Gaggero 2, 3, 4, 5 , Meng Fei 2, 3, 4, 5
Affiliation  

2,3-Dihydro-1,5-benzothiazepines have been obtained through a domino process involving a Michael addition of 2-aminothiophenols to chalcones, followed by in situ cyclization. Up to 98% chemical yields have been obtained at room temperature under essentially neutral conditions by using hexafluoro-2-propanol as an efficient medium.

中文翻译:

实用合成2,3-二氢-1,5-苯并硫氮杂s

已经通过多米诺法获得了2,3-二氢-1,5-苯并硫氮杂s,该方法包括将2-氨基硫酚的迈克尔加成至查耳酮,然后进行原位环化。使用六氟-2-丙醇作为有效介质,在基本上中性的室温下,室温下可获得高达98%的化学收率。
更新日期:2017-11-09
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