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◆ Organic letters2026-09-11

Access to (E)-2-(Benzo[1,2]dithiol-3-ylidene)acetonitriles via a Three-Component Reaction of o-Nitro-/Halobenzaldehydes, Cyanoacetates, and Sulfur.

Zhiwei Xu, Thi Thanh Tam Nguyen, Martial Toffano, Chloée Bournaud, Giang Vo-Thanh, Pascal Retailleau, Thanh Binh Nguyen

原始摘要(英文原文)· Original abstract
We report a sustainable, transition-metal-free multicomponent reaction for the step-economical assembly of (E)-2-(benzo[1,2]dithiol-3-ylidene)acetonitriles. This straightforward protocol utilizes elemental sulfur as a practical sulfur source, alongside active acetonitriles and o-nitro/halobenzaldehydes. Operating under mild conditions, the methodology provides a highly efficient route to novel disulfa heterocycles, expanding the toolkit for synthetic and medicinal chemistry.
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Access to (E)-2-(Benzo[1,2]dithiol-3-ylidene)acetonitriles via a Three-Component Reaction of o-Nitro-/Halobenzaldehydes, Cyanoacetates, and Sulfur. — 科研速览 Science Skim