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    1

    Diastereoselective Synthesis of Functionalized Angularly Fused Tricycles via an Organocascade Quadruple Reaction Involving Vinylogous 1,6/1,4/1,2/1,2-Addition Sequence

    This full text is not authorized to be published.

    • / Department of Chemistry /104/ Master
    • Author: Chang, Fu-Jie Advisor: Chen, Kwun-Min
    • An efficient three components organocascade quadruple reaction has been developed and successfull...
    • Clicks: 160Downloads: 0

    2

    Synthesis of Tricyclic chromanone Skeletons via Organocascade 1,6/Acetalization/Oxa-Michael Addition Sequence

    This full text is not authorized to be published.

    • / Department of Chemistry /105/ Master
    • Author: Kao, Chin-Wei Advisor: Chen, Kwun-Min
    • In this paper, organocascade triple reaction that catalyzed by small organic molecules have been ...
    • Clicks: 434Downloads: 0

    3

    Asymmetric Synthesis of 2,4,5,6-Tetrasubstituted Tetrahydropyrans via Domino 1,6-Addition /1,4-Oxa Michael Addition Sequence
    • / Department of Chemistry /109/ Master
    • Author: Liu, Fang-Nian Advisor: Chen, Kwun-Min
    • The use of organic catalyzed asymmetric domino reaction has become the current research trend, wh...
    • Clicks: 206Downloads: 9

    4

    Asymmetric Synthesis of Bicyclo[3.3.1]nonan-9-one Skeletons via Organocascade 1,6/1,4-Addition Sequence
    • / Department of Chemistry /104/ Master
    • Author: Wang, De-Chih Advisor: Chen, Kwun-Min
    • Organocascade reaction that catalyzed by organic small molecules is an efficient strategy for org...
    • Clicks: 172Downloads: 1

    5

    Organocatalytic Synthesis of Tricyclic Chroman Scaffold via 1,6-/Acetalization/1,4- Reaction Sequence

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    • / Department of Chemistry /106/ Master
    • Author: Chao, Tzu-Ching Advisor: Chen, Kwun-Min
    • An organic base catalyzed 1,6-/acetalization/1,4- cascade reaction between 1-(2'-hydroxyphenyl)bu...
    • Clicks: 348Downloads: 0

    6

    Highly Diastereoselective Synthesis of 2,3,4,5-Tetrasubstituted Pyrrolidines via Organocatalytic [3+2] Cycloaddition
    • / Department of Chemistry /108/ Master
    • Author: Yang, Chih-Ling Advisor: Chen, Kwun-Min
    • In the early synthesis of pyrrolidine, the reaction conditions were quite severe. However, in the...
    • Clicks: 340Downloads: 1

    7

    1.Divergent Synthesis of Coumarin Derivatives via Basecontrolled 1,6-Addition/Aldol and 1,6-Addition/Michael Cascades 2.Synthesis of Unprecedented Indeno[1,2-c]furan from αarylidene-1,3-indandione via Intramolecular Wittig Reaction

    This full text is not authorized to be published.

    • / Department of Chemistry /107/ Master
    • Author: Tseng, Ping-Yao Advisor: Lin, Wen-Wei
    • Part I : Herein, we demonstrated two vinylogous cascade reactions where in the chemoselectivity ...
    • Clicks: 219Downloads: 0

    8

    I. Base-controlled Catalytic Regioselective Aza-1,4/Formal Aza-1,6-addition Cascade Reaction for the Synthesis of Tetrahydroquinoline. II. Synthesis of Spiropentadiene Pyrazolones and 1H-Oxepino[2,3-c]pyrazoles from α,β,γ,δ-unsaturated Pyrazolones via Intramolecular Wittig Reaction

    This full text is not authorized to be published.

    • / Department of Chemistry /109/ Master
    • Author: Lin, Yi-Fang Advisor: Lin, Wen-Wei
    • I. We developed a strategy for the regioselective synthesis of two different skeletons of tetrahy...
    • Clicks: 251Downloads: 0

    9

    I. An Intramolecular Wittig Approach toward Heteroarenes : Synthesis of Isoxazoles and Chromenone-oximes. II. Base-controlled Regioselective Aza-1,4 / Aza-1,6-addition Cascade Reaction for Synthesis of Tetrahydroquinoline Derivatives

    This full text is not authorized to be published.

    10

    I. Chemoselective Synthesis of Substituted Isoxazole and Chromenone-oxime Derivatives via Intramolecular Wittig Reaction II. Diversity-Oriented Synthesis of Spiropentadiene Pyrazolones and 1H-Oxepino[2,3-c]pyrazoles via Phospha-1,6-Addition/O-Acylation/δ-C-Acylation/Cyclization/Wittig Strategy

    This full text is not authorized to be published.