Search Results - "GOINS, D. K"

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  1. 1

    Antigiardial Activity of Isoflavones from Dalbergia frutescens Bark by Khan, I. A, Avery, M. A, Burandt, C. L, Goins, D. K, Mikell, J. R, Nash, T. E, Azadegan, A, Walker, L. A

    “…Several isoflavones [formononetin (1), castanin (5), odoratin (6), glycitein (7), pseudobaptogenin (8), fujikinetin (9), and cuneatin (10)] were isolated from…”
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    Journal Article
  2. 2

    Structure−Activity Relationships of the Antimalarial Agent Artemisinin. 4. Effect of Substitution at C-3 by Avery, Mitchell A, Mehrotra, Sanjiv, Bonk, Jason D, Vroman, Jeffrey A, Goins, D. Keith, Miller, Robert

    Published in Journal of medicinal chemistry (19-07-1996)
    “…Novel antimalarial artemisinin analogs, 3-alkylartemisinins as well as 3-(arylalkyl)- and 3-(carboxyalkyl)artemisinins, were prepared via the synthetic…”
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    Journal Article
  3. 3

    A New Quassinoid from Castela texana by Dou, Jinhui, McChesney, James D, Sindelar, Robert D, Goins, D. Keith, Walker, Larry A

    “…A new quassinoid, 11-O-trans-p-coumaroyl amarolide (1) was isolated from Castela texana, and the structure was elucidated by spectroscopic analysis. Compound 1…”
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  4. 4

    Structure−Activity Relationships of the Antimalarial Agent Artemisinin. 3. Total Synthesis of (+)-13-Carbaartemisinin and Related Tetra- and Tricyclic Structures by Avery, Mitchell A, Fan, Pingchen, Karle, Jean M, Bonk, Jason D, Miller, Robert, Goins, D. Keith

    Published in Journal of medicinal chemistry (26-04-1996)
    “…Provided by total synthesis, endoperoxides 18, 20, and 22 underwent intramolecular oxymercuration−demercuration leading respectively to formation of an…”
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    Synthesis and biological activity of new potential antimalarial: 1H-pyrazolo[3,4-b]pyridine derivatives by Dias, L R, Freitas, A C, Barreiro, E J, Goins, D K, Nanayakkara, D, McChesney, J D, Dias, R S

    Published in Bollettino chimico farmaceutico (01-01-2000)
    “…The appearance of drug resistant Plasmodium falciparum malaria necessitates the search for novel antimalarial agents. Using the classical ring-bioisosterism…”
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