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Metal-Free Oxidative Spirocyclization of Alkynes with Sulfonylhydrazides Leading to 3‑Sulfonated Azaspiro[4,5]trienones

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NIAID Data Ecosystem2026-03-08 收录
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https://figshare.com/articles/dataset/Metal_Free_Oxidative_Spirocyclization_of_Alkynes_with_Sulfonylhydrazides_Leading_to_3_Sulfonated_Azaspiro_4_5_trienones/2166334
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A novel and direct oxidative spirocyclization of arylpropiolamides with sulfonylhydrazides leading to 3-sulfonated azaspiro­[4,5]­trienones has been developed under metal-free conditions. The reaction is performed in a tandem manner constituted by the sequential sulfonylation of alkynes, ipso-carbocyclization, dearomatization, hydration, and oxidation processes, providing a convenient and efficient approach to various sulfonated azaspiro­[4,5] trienones of biological importance.
创建时间:
2016-02-13
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