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One pot preparation of α-dithioacetal/α-diselenoacetal amides via a dual-C–S/C–Se bond formation and C–C bond cleavage cascade of 3-oxo-butanamides†‡
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2018-06-13 00:00:00 , DOI: 10.1039/c8qo00435h
Jiao-xia Zou 1, 2, 3, 4 , Yong-qiang Wang 1, 2, 3, 4 , Long-tao Huang 1, 2, 3, 4 , Yi Jiang 1, 2, 3, 4 , Jin-hong Chen 1, 2, 3, 4 , Long-qing Zhu 1, 2, 3, 4 , Yu-hang Yang 1, 2, 3, 4 , Yi-yue Feng 1, 2, 3, 4 , Xue Peng 1, 2, 3, 4 , Zhen Wang 1, 2, 3, 4, 5
Affiliation  

A new and practical approach to α-dithioacetal/α-diselenoacetal amides has been developed, combining sequential functionalization of amides and a C–C bond cleavage strategy. In this reaction, various α-dithioacetal/α-diselenoacetal amides from 3-oxo-butanamides were prepared in one step with good regioselectivity and functional group tolerance.

中文翻译:

一锅制备α-二硫缩醛/α-diselenoacetal酰胺通过的3-氧代- butanamides双C-S / C-Se键的形成和C-C键断裂级联†往最

已经开发出一种新的实用的α-二硫缩醛/α-二硒缩醛酰胺方法,该方法结合了酰胺的顺序功能化和CC键裂解策略。在该反应中,一步制得了3-氧代丁酰胺中的各种α-二硫缩醛/α-二硒缩醛酰胺,具有良好的区域选择性和官能团耐受性。
更新日期:2018-06-13
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