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2 edition of constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives found in the catalog.

constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives

Samuel Cox Hooker

constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives

memorial volume to Samuel C. Hooker, 1864-1935

by Samuel Cox Hooker

  • 79 Want to read
  • 18 Currently reading

Published by Mack Printing Company in Easton, Pa .
Written in English

    Subjects:
  • Naphthoquinone.,
  • Lapachol.,
  • Lomatiol.

  • Edition Notes

    Collected works of Dr. Hooker and collaborators on the subject of lapachol chemistry reprinted from the American Chemical Journal (1889), the Journal of the Chemical Society (1892-1896) and the Journal of the American Chemical Society (1936) with an obituary sketch of Dr. Hooker, by C. A. Browne, from the Journal of the Chemical Society (1936) cf. Pref.

    Other titlesHydroxynaphthoquinone derivatives.
    Statementedited by Louis F. Fieser.
    ContributionsFieser, Louis Frederick, 1899-, Browne, Charles Albert, 1870-1947.
    Classifications
    LC ClassificationsQD341.K2 H78
    The Physical Object
    Paginationvi, 135 p.
    Number of Pages135
    ID Numbers
    Open LibraryOL14142571M
    LC Control Number37003633


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Constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives by Samuel Cox Hooker Download PDF EPUB FB2

Get this from a library. The constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives; memorial volume to Samuel C. Hooker. [Samuel Cox Hooker; Louis F Fieser; Charles Albert Browne]   Samuel Cox Hooker (* April in Brenchley, Kent; † Oktober in Brooklyn) war ein englischer Chemiker in den USA.

Seine Eltern waren der Architekt John Marshall Hooker und Ellen, geb. Cox. Ab studierte er an der zu der Zeit wiedereröffneten Normal School of Science and Royal School of Mines (heute Royal College of Science) und ab in München bei Bamberger, wo er   The constitution and properties of lapachol, lomatiol, and other hydroxynapthoquinone derivatives;: Memorial volume to Samuel C.

Hooker, ; Mack Printing Company, Literatur C. Browne: Journal of the Chemical Society,S. (Online) The constitution and properties of lapachol, lomatiol, and other hydroxynaphthoquinone derivatives; Edgar Fahs Smith,?: A history of the American Chemical Society, seventy-five eventful years: The life and chemical services of Frederick Accum: Magic squares and cubes: Methods of honey testing for bee Investigation of the action of lapachol and -lapachone (2), as well as other naphthoquinone derivatives, against the epimastigote form of T.

cruzi began in with a series of efforts by the Conclusions: The naphthotriazolyloxoquinoline derivatives were obtained in good to moderate yields, and one of them, 12c, exhibited strong and selective antitumor :// Antileishmanial activity of lapachol 1 Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol.Antileishmanial Activity of Lapachol Analogues /_Antileishmanial_activity_of_lapachol_analogues.

Zusammenfassung. Die vorliegende Übersicht stellt zum Teil die Erweiterung eines vor nur wenigen Jahren erschienenen Referates über dasselbe Gebiet dar ().Seit damals ist aber eine erfreulich große Anzahl wertvoller Arbeiten über verschiedene Aspekte der Biochemie der Chinone erschienen, so daß auf manchen Teilgebieten eine völlige Neugruppierung des Stoffes erforderlich :// Hooker SC () Lomatiol, Part II, Its occurrence, constitution, relation to, and conversion into lapachol, Also a synthesis of lapachol.

J Am Chem Soc – CrossRef Google Scholar Howells RE, Peters W, Fullard J () The chemotherapy of rodent :// Gabe Podcast Sakthi Monk Media Gentleman and Lady's Book of Politeness and Propriety of Deportment, The by CELNART, Élisabeth Olivier I LOVE PACA Podcast Mr.J Featured software All software latest This Just In Old School Emulation MS-DOS Games Historical Software Classic PC Games Software The incorporation of the amino functional group at the 2-position of 1,4-naphthoquinone has led to the generation of enhanced biological and physiochemical properties and also the constitution of CELLULAR OXIDATION SYSTEMS CELLULAR OXIDATION SYSTEMS E.

Guzman Barron SYSTEMS E. GUZMAN Lasker Foundation for Medical Research and Department of Chicago of Medicine, the 7 â niversit?l Combustion of foodstuffs through oxygen was Lavoisierâ s () conception of respiration.

It is still ours, and for this reason t-he term Experiments since Chapter 27 Aromatic Compounds with Condensed Nuclei: Naphthalene and Related Compounds* N.

CAMPBELL 1. The naphthalene nucleus (a) Constitution Naphthalene, C~oHs, was first isolated from coal tar, still the main source of the hydrocarbon, by Garden in and its composition was determined by Michael Faraday in This banner text can have markup.

web; books; video; audio; software; images; Toggle Request PDF | Synthesis of 2,3-Disubstituted 1,4-Naphthoquinones via Metal-Free C(sp2)-H Functionalization Followed by Suzuki Cross-Coupling Reactions | A   Irradiation of a warm aqueous solution of lawsone gives a 40 per cent yield of 3-bi-2, 2' -cO- naphthoquinone which, by several direct procedures, may be converted into the cCj^C'- (70 per cent), the d3,p~ (85 per cent), or the &/3 1 - (86 per cent) anhydrides II.

The Chemistry of Lapachol (i) and Lomatiol Full text of "Textile chemicals [electronic resource]: environmental data and facts" See other formats Full text of "Oxidation-reduction potentials in bacteriology and biochemistry" See other formats A CHRONOLOGICAL LISTINGOF SELECTED BOOK TITLES1'0ILLIJSTKATE THE WELL-ENTRENCHED USAGE OF "SECONDARY METABOLISM" AND RELATED TEnMSU Author(s) Title Lehrbuch der Pflanzenphysiologie, Vol.

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