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Regioselective allene hydroarylation via one-pot allene hydrosilylation/Pd-catalyzed cross-coupling.


ABSTRACT: Advances in hydroarylation have been achieved by the development of a one-pot regioselective allene hydrosilylation/Pd(0)-catalyzed cross-coupling protocol. The regioselectivity is primarily governed by N-heterocyclic carbene (NHC) ligand identity in the hydrosilylation step and is preserved in the subsequent cross-coupling reaction. This methodology affords streamlined access to functionalized 1,1-disubstituted alkenes with excellent regiocontrol.

SUBMITTER: Miller ZD 

PROVIDER: S-EPMC4201326 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

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Regioselective allene hydroarylation via one-pot allene hydrosilylation/Pd-catalyzed cross-coupling.

Miller Zachary D ZD   Montgomery John J  

Organic letters 20141002 20


Advances in hydroarylation have been achieved by the development of a one-pot regioselective allene hydrosilylation/Pd(0)-catalyzed cross-coupling protocol. The regioselectivity is primarily governed by N-heterocyclic carbene (NHC) ligand identity in the hydrosilylation step and is preserved in the subsequent cross-coupling reaction. This methodology affords streamlined access to functionalized 1,1-disubstituted alkenes with excellent regiocontrol. ...[more]

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