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Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling.

Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Research Abstract Details 

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  • Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Abstract Text:

    estelle Estelle ,qian huQian Hu,ei-ichi negishiEi-ichi Negishi,

    Iteration of a Pd-catalyzed reaction of alkynyl- and oligoynylzincs with (E)-ICH=CHCl followed by metalation-termination with electrophiles(E) has provided a linear route to conjugated tri- and tetraynes, and Pd-catalyzed monoalkynylation of 1,1-dibromoenynes accompanied by dehydrobromination has provided a convergent route to conjugated tri- , tetra- , and pentaynes. Both display unprecedented high efficiency and selectivity. [reaction: see text]

    Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Publishing Authors By Initials

    e E ,q huQ Hu,e negishiE Negishi,

    For similar inorganic chemicals: elements: metals, heavy: palladium research abstracts see: inorganic chemicals: elements: metals, heavy: palladium research

    PUBMED ID PMID:

    MEDLINE DATE:

    Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Organic letters

    VOLUME: 8

    Page Numbers: 5773-6

    Journal Abbreviation: Org. Lett.

    ISSN: 1523-7060

    DAY: 7

    MONTH: Dec

    YEAR: 2006

    Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100890393

    Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Keywords Mesh Terms:

    KEYWORDS: Palladium

    MESH TERMS: chemistry

    Chemical & Substance for Abstract: Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling. Information

    Substance Name: Palladium

    Registry Number: 7440-05-3

    Grant and Affiliation Information for Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling.

    AFFILIATION: Herbert C. Brown Laboratories of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: GM 36792

    ACRONYM: GM

    MEDLINETA: Org Lett

    REFSOURCE:

    DATABASENAME:

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    Highly efficient and selective synthesis of conjugated triynes and higher oligoynes of biological and materials chemical interest via palladium-catalyzed alkynyl-alkenyl coupling Related Publications

     

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