Sequential molecular conjugation using thiophene S,S-dioxides bearing a clickable functional group

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Abstract

Electron-deficient thiophene dioxides have been found to react rapidly with a bicyclo[6.1.0]non-4-yne derivative to afford benzocyclooctenes in excellent yields. Thiophene dioxides bearing a clickable functional group served as efficient bisreactive platform molecules that enabled sequential molecular conjugation in a simple operation.

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Meguro, T., Yoshida, S., & Hosoya, T. (2017). Sequential molecular conjugation using thiophene S,S-dioxides bearing a clickable functional group. Chemistry Letters, 46(8), 1137–1140. https://doi.org/10.1246/cl.170426

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