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    Highly Enantioselective Rhodium-Catalyzed Transfer Hydrogenation of Tetrasubstituted Olefins: Application toward the Synthesis of GPR40 Agonist MK-2305

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    A highly efficient enantioselective synthesis for the potent G-protein-coupled receptor 40 agonist MK-2305 was developed. The key tetrasubstituted olefin was prepared via a stereoselective Mukaiyama aldol reaction/elimination sequence. The highly enantioselective rhodium-catalyzed transfer hydrogenation of the tetrasubstituted olefin afforded the target compound MK-2305 in excellent optical and chemical purity. The key asymmetric transfer hydrogenation proceeds in excellent yields and enantioselectivities for a variety of substrates. The superior reactivity of the tethered catalysts was revealed by NMR studies

    Highly Enantioselective Rhodium-Catalyzed Transfer Hydrogenation of Tetrasubstituted Olefins: Application toward the Synthesis of GPR40 Agonist MK-2305

    No full text
    A highly efficient enantioselective synthesis for the potent G-protein-coupled receptor 40 agonist MK-2305 was developed. The key tetrasubstituted olefin was prepared via a stereoselective Mukaiyama aldol reaction/elimination sequence. The highly enantioselective rhodium-catalyzed transfer hydrogenation of the tetrasubstituted olefin afforded the target compound MK-2305 in excellent optical and chemical purity. The key asymmetric transfer hydrogenation proceeds in excellent yields and enantioselectivities for a variety of substrates. The superior reactivity of the tethered catalysts was revealed by NMR studies

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    BIT 2305 HCI---mutur

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    SMA 2305 Complex Analysis

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    HBA 2305-Bankruptcy-BCom-Y3S2 -Supp. (2)

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    HBA 2305-Bankruptcy-BCom-Y3S2 -Supp. (2

    HBA 2305-Bankruptcy-BCom-Y3S2 -Supp.

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    HBA 2305-Bankruptcy-BCom-Y3S2 -Supp

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    A photograph print showing Chesapeake & Ohio (C&O) 2305, 2-8-2 (class K-3-a), Stephens, KY

    HBA 2305-Bankruptcy-BCom Y3S2 -Main

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    HBA 2305-Bankruptcy-BCom Y3S2 -Mai
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