دورية أكاديمية

Light-promoted photocatalyst-free and redoxneutral hydrosulfonylation of unactivated alkenes using sulfinic acid.

التفاصيل البيبلوغرافية
العنوان: Light-promoted photocatalyst-free and redoxneutral hydrosulfonylation of unactivated alkenes using sulfinic acid.
المؤلفون: Yibo Song, Cheng Li, Xueyuan Hu, Hongdie Zhang, Yujian Mao, Xiachang Wang, Chen Wang, Lihong Hu, Jianming Yan
المصدر: Green Chemistry; 6/7/2024, Vol. 26 Issue 11, p6578-6583, 6p
مصطلحات موضوعية: SULFINIC acids, ALKENES, LIGHT absorption, NATURAL products, RADICALS (Chemistry), BRONSTED acids
مستخلص: A hydrosulfonylation reaction of unactivated alkenes with sulfinic acids was realized under light irradiation. This reaction features photocatalyst- and additive-free conditions. A diverse set of unactivated alkenes can be transformed into alkyl-substituted sulfones with good yields and anti-Markovnikov regioselectivity. The present protocol was amenable to gram-scale synthesis, as well as late-stage modification of drugs and natural products. Preliminary mechanistic studies on UV-visible light absorption suggested the key role of sulfinic acid as a light-absorbing species. DFT calculations also shed light on the mechanism of this reaction, which may involve a radical chain pathway. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:14639262
DOI:10.1039/d4gc00440j