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Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle.

Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Research Abstract Details 

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  • Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Abstract Text:

    yonghong ganYonghong Gan,thomas a spencerThomas A Spencer,

    Photoactivatable analogues 4-6 of cholesterol (1), having their cross-linking site in the ring D sterol region, have been synthesized starting from bromotetralone 14 via enantioselective Robinson annulation to enone 13 and Suzuki carbonylative coupling to the appropriate phenylboronic acid. Each of 4-6 was shown to substitute successfully for 1 in an assay of apo A-I-induced cellular cholesterol efflux, indicating that these analogues equilibrated with 1 in all major cellular pools.

    Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Publishing Authors By Initials

    y ganY Gan,ta spencerTA Spencer,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: The Journal of organic chemistry

    VOLUME: 71

    Page Numbers: 5870-5

    Journal Abbreviation:

    ISSN: 0022-3263

    DAY: 4

    MONTH: Aug

    YEAR: 2006

    Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 2985193

    Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle. Keywords Mesh Terms:

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    Grant and Affiliation Information for Cholesterol surrogates incorporating a benzophenone as part of the sterol tetracycle.

    AFFILIATION: Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Org Chem

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