Results 81 to 90 of about 2,769 (197)

Ueber Acridon [PDF]

open access: yesJustus Liebigs Annalen der Chemie, 1893
C. Graebe, K. Lagodzinski
openaire   +1 more source

Some synthetical experiments on organic bases [PDF]

open access: yes, 1934
SOME SYNTHETICAL EXPERIMENTS ON ORGANIC BASES: The Thesis now presented is an account of some work undertaken by the Author with the primary object of preparing bases suitable for test as anti-malarials but deals in some detail with some important ...
Nisbet, Hugh Bryan
core  

Synthesis and spectral studies of methyl heterocylic systems [PDF]

open access: yes, 1979
2-Carboxy-2?-methyldiphenyl sulfide was prepared by the Ullmann reaction and cyclodehydrated by sulfuric acid to afford 4-methylthioxanthone. 1-Methylthioxanthone was separated from the reaction mixture obtained upon cyclodehydration of 2-carboxy-3f ...
Doyle, Paul P.
core   +1 more source

Acridone Derivatives from Atalantia monophyla Inhibited Cancer Cell Proliferation through ERK Pathway. [PDF]

open access: yesMolecules, 2022
Gao WY   +8 more
europepmc   +1 more source

Xanthone-1,2,4-triazine and Acridone-1,2,4-triazine Conjugates: Synthesis and Anticancer Activity. [PDF]

open access: yesPharmaceuticals (Basel), 2023
Santra S   +11 more
europepmc   +1 more source

Ueber Phenylantranilsäure und Acridon [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1892
C. Graebe, K. Lagodzinski
openaire   +1 more source

The nucleophillic substitution of various chloroanthraquinones of their possible rearrangement via aryne intermediates [PDF]

open access: yes, 1977
The work in this thesis deals mainly with nucleophilic substitution of chloroanthraquinones as a route to various starting materials which might rearrange, via aryne intermediates to afford fused-ring heterocy1ic carboxylic acids.
Ruediger, Edward H.
core   +1 more source

Synthèse régiospécifique de quinones hétérocycliques azotées [PDF]

open access: yes, 1994
"Au cours des dernières années, les systèmes quinoniques hétérocycliques ont connu un essor fulgurant en raison du potentiel pharmacologique important déployé par certaines de ces substances naturelles. Devant l'intérêt accru suscité par ces composés, il
Mongrain, Colette
core  

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