区域选择性
化学
环加成
磺酰
部分
极性效应
乙炔
功能群
醋酸乙烯酯
砜
高分子化学
双键
选择性
正在离开组
有机化学
戒指(化学)
乙烯基聚合物
立体化学
钯
结构异构体
三键
群(周期表)
药物化学
作者
Amitabha Bose,Tanmaya Pathak
标识
DOI:10.1002/slct.202507305
摘要
ABSTRACT This study explores the effect of an additional electron‐withdrawing sulfonyl group on the regioselectivity of triazole formation using vinyl bissulfones, a new class of acetylene equivalent and leads to the synthesis of a wide range of sulfonylated triazoles. The selectivity was influenced by the positioning of the second electron withdrawing vinyl sulfone group, which enhances the electron deficient nature of the double bond and also acts as a leaving group. Internal vinyl bissulfones generated a complex mixture of products. However, terminal vinyl bissulfones, regioselectively produced two types of 1,4‐disubstituted 1,2,3‐triazoles functionalized either with a CH 2 SO 2 Ar moiety or the ArSO 2 group directly attached to the triazole ring depending on the nature of the starting material. These metal‐free reactions, executed in water, are a new addition to the eliminative azide‐olefinic cycloaddition category of reactions. The results suggest that modified vinyl bissulfones are inexpensive and readily available starting materials for the synthesis of two distinct varieties of 1,4‐disubstituted sulfonylated 1,2,3‐triazoles in a regioselective fashion via unconventional routes.
科研通智能强力驱动
Strongly Powered by AbleSci AI