Nickel-catalyzed reductive 1,3-diene formation from the cross-coupling of vinyl bromides.

Org Biomol Chem

Center for Supramolecular Chemistry and Catalysis and Department of Chemistry, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China.

Published: June 2021

Facile construction of 1,3-dienes building upon cross-electrophile coupling of two open-chain vinyl halides is disclosed in this work, showing moderate chemoselectivities between the terminal bromoalkenes and internal vinyl bromides. The present method is mild and tolerates a range of functional groups and can be applied to the total synthesis of a tobacco fragrance solanone.

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Source
http://dx.doi.org/10.1039/d1ob00791bDOI Listing

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