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    Results 221-230 of 307.

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    221Production of potent antidiabetic compounds from shrimp head powder via Paenibacillus conversion

    Van Bon Nguyen; San-Lang Wang2019
    [Graduate Institute & Department of Chemistry] Journal Article
    Process Biochemistry 76, p.18-24
    marine chitinous materials, Molecules 23 (2018) 1124. V.B. Nguyen, S.L. Wang, N.T. Nhan, T.H. Nguyen, N.P.D. Nguyen, D.H. Nghi, N.M. Cuong, New

    222A semiempirical study of C24N4 and its boron-nitrogen analogs

    王伯昌; Wang, Bo-cheng; 1996
    [Graduate Institute & Department of Chemistry] Journal Article
    International journal of quantum chemistry 57(3), pp.465-470
    (EF) with a mixamum step size of 0.1000. To carry out the calculatiuns on the fullerene-sized molecules, the SGI workstation and the MOPAC package

    223Preparation, electrochemical and spectral properties of N-methylated pyridylethynyl porphyrins

    王文竹2004-01-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Dalton Transaction 2004, pp.456
    the entire molecules of Zn2 and Zn6 are reduced for their first and second reductions. This is also different from what have been reported

    224Pyridine-Catalyzed Double C–N Coupling Reaction of an Isocyanate with Two Benzynes

    Lee, Yi-Hsien; Chen, Yen-Chung; 2012-01
    [Graduate Institute & Department of Chemistry] Journal Article
    European Journal of Organic Chemistry 2012(2), pp.247–250
    of H2O and two benzyne molecules. Reactions carried out in CH3CN at 70 °C were optimal; neither increased nor de- creased temperatures improved

    225Synthesis and stability study of isocyano aryl boronate esters and their synthetic applications

    Hao-Ping Fang; Chia-Chieh Fu; 2016-03-17
    [Graduate Institute & Department of Chemistry] Journal Article
    RSC Advances 6, pp.30362-30371
    Boronic acid-containing molecules are used in a wide range of organic reactions, including Suzuki–Miyaura coupling,4 Chan–Lam coupling,5 Liebeskind

    226Synthesis and stability study of isocyano aryl boronate esters and their synthetic applications

    Fang, Hao-Ping; Fu, Chia-Chieh; 2016-03-17
    [Graduate Institute & Department of Chemistry] Journal Article
    RSC Advances 6(36), p.30362-30371
    molecules are used in a wide range of organic reactions, including Suzuki–Miyaura coupling,4 Chan–Lam coupling,5 Liebeskind–Srogl coupling,6

    227Synthesis, structure and magnetic properties of mononuclear [Mn(2,2′-bipyrimidine)2(H2O)2][ClO4]2 and polynuclear [Mn(2,2′-bipyrimidine)(NO3)2] complexes

    Hong, D. M.; 魏和祥; 1996-07
    [Graduate Institute & Department of Chemistry] Journal Article
    Polyhedron 15(14), pp.2335-2340
    followed by full-matrix least-squares refinement. The ORTEP plots of the molecules are shown in Figs 1 (1) end 2 (2 with a manganese environment

    228Ab Initio Study of the Reaction Mechanisms of NiO and NiS with H2

    黃德彥; Hwang, Der-yan; 2002-01-24
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of physical chemistry A 106(3), pp.520-528
    orbital of H2 to the empty 3ó orbital of NiO and does not depend on the planarity of tho mutual orientation of the twa molecules. On the other hand

    2293-Deoxy-3-thia-1.alpha.,25-dihydroxyvitamin D3 and its 1.beta.-epimer: synthesis and biological evaluation

    李世元; Lee, Adam Shih-yuan; 1992
    [Graduate Institute & Department of Chemistry] Journal Article
    The Journal of organic chemistry 57(14), pp.3846-3854
    =  ; Y = OH analogues5*1 have emerged as desirable target molecules for synthesis and biological evaluation. The purpose of this paper is to report

    230Nanomaterial Enhanced Gene Expression in Yeast Cells

    簡素芳; Chien, Su-fang; 2008-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of Nanomaterials 2008, pp.391497(9pages)
    . This is the location in the cell where DNA molecules are copied for translation into proteins or are multiplied for cell division. Xu et al. [4] studied the real-time


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