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Highly selective reactions of unbiased alkenyl halides and alkylzinc halides: Negishi-Plus couplings.

ABSTRACT: High yielding stereo- and chemoselective Pd-catalyzed cross-couplings in THF at room temperature of alkenyl iodides and bromides with primary and secondary alkyl zinc iodides have been developed with the aid of N-methyimidazole as the key additive.

SUBMITTER: Krasovskiy A

PROVIDER: S-EPMC3365517 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Highly selective reactions of unbiased alkenyl halides and alkylzinc halides: Negishi-Plus couplings.

Krasovskiy Arkady A Lipshutz Bruce H BH

Organic letters 20110708 15

High yielding stereo- and chemoselective Pd-catalyzed cross-couplings in THF at room temperature of alkenyl iodides and bromides with primary and secondary alkyl zinc iodides have been developed with the aid of N-methyimidazole as the key additive. ...[more]

PMID: 21739947

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