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Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents.


ABSTRACT: A stereoconvergent method for the catalytic asymmetric Negishi cross-coupling of racemic secondary propargylic halides with arylzinc reagents has been developed. Neither family of compounds has previously been shown to be a suitable partner in such coupling processes. From a practical point of view, it is noteworthy that the catalyst components (NiCl2.glyme and pybox ligand 1) are commercially available.

SUBMITTER: Smith SW 

PROVIDER: S-EPMC2626171 | biostudies-literature | 2008 Sep

REPOSITORIES: biostudies-literature

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Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents.

Smith Sean W SW   Fu Gregory C GC  

Journal of the American Chemical Society 20080903 38


A stereoconvergent method for the catalytic asymmetric Negishi cross-coupling of racemic secondary propargylic halides with arylzinc reagents has been developed. Neither family of compounds has previously been shown to be a suitable partner in such coupling processes. From a practical point of view, it is noteworthy that the catalyst components (NiCl2.glyme and pybox ligand 1) are commercially available. ...[more]

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