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Iron(III)-Catalyzed Synthesis of 2-Alkyl Homoallyl Sulfonyl Amides: Antiproliferative Study and Reactivity Scope of Aza-Prins Cyclization
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2022-08-03 , DOI: 10.1021/acs.joc.2c01267
Rubén M Carballo 1 , José M Padrón 2 , Israel Fernández 3 , Daniel A Cruz 4 , Luana Grmuša 4 , Víctor S Martín 2 , Juan I Padrón 4
Affiliation  

A direct, catalytic, and complementary method to obtain 2-substituted homoallyl sulfonyl amides is described, starting from sulfonyl amides, aldehydes, and allyltrimethylsilane using iron(III) chloride as a sustainable catalyst. The scope of the process and the reactivity in aza-Prins cyclization is evaluated and supported by density functional theory (DFT) studies. Finally, an evaluation of the antiproliferative activity for this family of sulfonyl amides is also included.

中文翻译:

铁(III)-催化合成2-烷基高烯丙基磺酰胺:氮杂-普林斯环化的抗增殖研究和反应范围

描述了一种直接、催化和互补的方法来获得 2-取代的高烯丙基磺酰胺,从磺酰胺、醛和烯丙基三甲基硅烷开始,使用氯化铁 (III) 作为可持续催化剂。密度泛函理论 (DFT) 研究评估和支持了氮杂-普林斯环化过程的范围和反应性。最后,还包括对该磺酰酰胺家族的抗增殖活性的评估。
更新日期:2022-08-03
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