Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications

There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene via 1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes via 1,2-difunctionalization in a desired manner is not as easy as it might be...

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Veröffentlicht in:Science China. Chemistry 2024-03, Vol.67 (3), p.936-944
Hauptverfasser: Yang, Bo, Li, Kangkui, Wang, Yongdong, Zhu, Shifa
Format: Artikel
Sprache:eng
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Zusammenfassung:There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene via 1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes via 1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio- and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous ( E )- β -bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes.
ISSN:1674-7291
1869-1870
DOI:10.1007/s11426-023-1871-y