Search Results - "MAITI, Arup"

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  1. 1

    Asymmetric total syntheses of panaxytriol and panaxydol, potent antitumor agents from Panax ginseng by Yadav, J.S, Maiti, Arup

    Published in Tetrahedron (10-06-2002)
    “…A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d-arabinose using base induced double elimination of 4,5- O-isopropylidene propargyl chloride…”
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  2. 2

    Zapotin Prevents Mouse Skin Tumorigenesis During the Stages of Initiation and Promotion by CUENDET, Muriel, OTEHAM, Carol P, MAITI, Arup, CRAIG, Bruce A, CUSHMAN, Mark, MOON, Richard C, PEZZUTO, John M

    Published in Anticancer research (01-11-2008)
    “…Background: Zapotin, a flavonoid associated with Casimiroa edulis, was isolated as part of a program to discover natural inhibitors of carcinogenesis. Zapote…”
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  3. 3
  4. 4

    Synthesis and Biological Evaluation of (±)-Abyssinone II and Its Analogues as Aromatase Inhibitors for Chemoprevention of Breast Cancer by Maiti, Arup, Cuendet, Muriel, Croy, Vicki L, Endringer, Denise C, Pezzuto, John M, Cushman, Mark

    Published in Journal of medicinal chemistry (14-06-2007)
    “…An efficient and economical synthesis of the naturally occurring aromatase inhibitor abyssinone II was performed. The synthesis features an optimized aromatic…”
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  5. 5

    Synthesis of Casimiroin and Optimization of Its Quinone Reductase 2 and Aromatase Inhibitory Activities by Maiti, Arup, Reddy, P. V. Narasimha, Sturdy, Megan, Marler, Laura, Pegan, Scott D, Mesecar, Andrew D, Pezzuto, John M, Cushman, Mark

    Published in Journal of medicinal chemistry (09-04-2009)
    “…An efficient method has been developed to synthesize casimiroin (1), a component of the edible fruit of Casimiroa edulis, on a multigram scale in good overall…”
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  6. 6
  7. 7

    Synthesis and Cancer Chemopreventive Activity of Zapotin, a Natural Product from Casimiroa edulis by Maiti, Arup, Cuendet, Muriel, Kondratyuk, Tamara, Croy, Vicki L., Pezzuto, John M., Cushman, Mark

    Published in Journal of medicinal chemistry (25-01-2007)
    “…An efficient method has been developed to synthesize zapotin (5,6,2‘,6‘-tetramethoxyflavone), a component of the edible fruit Casimiroa edulis, on a multigram…”
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  8. 8

    From Dimerization, to Cycloaddition, to Atom Transfer Cyclization:  The Further Chemistry of TMM Diradicals by Maiti, Arup, Gerken, James B, Masjedizadeh, Mohammad R, Mimieux, Yvette S, Little, R. Daniel

    Published in Journal of organic chemistry (10-12-2004)
    “…We describe [a] the first examples of intramolecular cycloaddition of a TMM diyl to a remotely tethered aldehyde, [b] the effect of a Lewis acid upon the…”
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  9. 9

    A highly efficient and practical method for the synthesis of chiral polyhydroxy diacetylenic alcohols by Yadav, J.S, Maiti, Arup

    Published in Tetrahedron letters (04-06-2001)
    “…An efficient protocol for the synthesis of chiral polyhydroxy diacetylenic alcohols from chiral 4,5- O-isopropylidene propargyl chlorides using strong bases is…”
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  10. 10

    Asymmetric Synthesis of (+)-allo-Quercitol and (+)-talo-Quercitol via Free Radical Cycloisomerization of an Enantiomerically Pure Alkyne-Tethered Aldehyde Derived from a Carbohydrate by YADAV, J. S., MAITI, Arup, SANKAR, A. Ravi, KUNWAR, A. C.

    Published in Journal of organic chemistry (14-12-2001)
    “…We describe for the first time the free radical cyclization of enantiomerically pure alkyne-tethered aldehydes obtained from a carbohydrate (6, 7). The…”
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  11. 11

    Asymmetric Synthesis of (+)-a llo-Quercitol and (+)-t alo-Quercitol via Free Radical Cycloisomerization of an Enantiomerically Pure Alkyne-Tethered Aldehyde Derived from a Carbohydrate by Yadav, J. S, Maiti, Arup, Sankar, A. Ravi, Kunwar, A. C

    Published in Journal of organic chemistry (14-12-2001)
    “…We describe for the first time the free radical cyclization of enantiomerically pure alkyne-tethered aldehydes obtained from a carbohydrate (6, 7). The…”
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    Journal Article
  12. 12

    ONE-POT OXIDATION AND WITTIG OLEFINATION OF ALCOHOLS USING O-IODOXYBENZOIC ACID AND STABLE WITTIG YLIDE by Maiti, Arup, Yadav, J. S.

    Published in Synthetic communications (01-01-2001)
    “…Benylic, allylic, and propargylic alcohols, as well as diols, can be oxidized with o-iodoxybenzoic acid (IBX) in the presence of stabilized Wittig ylide [1] to…”
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