Results 171 to 180 of about 4,972 (216)
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The Journal of Organic Chemistry, 2000
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Dajie Li, Baoping Zhao, Edmond J. LaVoie
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Dajie Li, Baoping Zhao, Edmond J. LaVoie
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ChemInform, 2015
AbstractThe title phenanthridines are obtained by aza Diels—Alder reactions and dehydrogenation aromatization reactions of in situ generated benzyne with N‐benzylideneanilines.
Wang Xueli+5 more
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AbstractThe title phenanthridines are obtained by aza Diels—Alder reactions and dehydrogenation aromatization reactions of in situ generated benzyne with N‐benzylideneanilines.
Wang Xueli+5 more
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Synthesis of phenanthridine derivatives
Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 1966Hydrogenated derivatives of 9-arylphenanthridine are formed when 1-cyclohexenyl ethyl ether is reacted with Schiff bases in the presence of BF3.
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A New Synthesis of Phenanthridine Derivatives
HETEROCYCLES, 1983AbstractDie Homophthalimide (I) werden mit Methylvinylketon (II) zu den Verbindungen (III) umgesetzt, die zu den isomeren Hexahydrophenanthridinonen (V) und (VI) cyclisiert werden.
Hideo Iida+4 more
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Studies in the phenanthridine series—III
Tetrahedron, 1971Abstract Kinetic data are reported for the quaternisation of several alkylphenanthridines and for the reactions of some 6-chlorophenanthridines with various nucleophiles. The enhanced (and anomalous) reactivity shown by 6-chloro-1,10-dimethylphenanthridine is explained in terms of relief of steric strain. NMR data and p K a , values are reported.
G.L. Turner, B.R.T. Keene
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ChemInform Abstract: Synthesis of Phenanthridine Derivatives via Photolysis.
ChemInform, 2011An improved photochemical method for producing the prolifically bioactive phenanthridine system is reported. A wide variety of derivatives were obtained in two steps in yields ranging from 31 to 95%.
Stefan Bräse+3 more
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Journal of Organic Chemistry, 2018
Simple treatment of 2-cyanobiaryls with methyllithium, ethylmagnesium bromide, butyllithium, phenyllithium, p-methylphenyllithium, etc., followed by the reaction with water and then with molecular iodine at 60 °C provided efficiently 6-methyl-, 6-ethyl-,
Atsushi Kishi, K. Moriyama, H. Togo
semanticscholar +1 more source
Simple treatment of 2-cyanobiaryls with methyllithium, ethylmagnesium bromide, butyllithium, phenyllithium, p-methylphenyllithium, etc., followed by the reaction with water and then with molecular iodine at 60 °C provided efficiently 6-methyl-, 6-ethyl-,
Atsushi Kishi, K. Moriyama, H. Togo
semanticscholar +1 more source
The chemotherapy of phenanthridine compounds
Journal of the Society of Chemical Industry, 1947AbstractAn account is given of the preparation of various phenanthridine compounds and of their use in chemotherapy. Several of the compounds are curative of bovine trypanosomiasis, an African disease transmitted by the tsetse fly, and promise to be of great value in the African colonics.
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Journal of Organic Chemistry, 2018
A room-temperature metal-free method for generating highly unstable methyl radical was realized from the combination of PhI(OAc)2 and 2-nitropropane, which provides an efficient approach to methylated phenanthridines and isoquinolines.
Shi‐Chao Lu+5 more
semanticscholar +1 more source
A room-temperature metal-free method for generating highly unstable methyl radical was realized from the combination of PhI(OAc)2 and 2-nitropropane, which provides an efficient approach to methylated phenanthridines and isoquinolines.
Shi‐Chao Lu+5 more
semanticscholar +1 more source
ChemInform, 2012
Abstract The zwitterions generated from phenanthiridine and dialkyl acetylenedicarboxylates (DAADs) react with a variety of arylidenemalononitriles, affording substituted pyrido[1,2-f]phenanthridines.
Mahdi Hatamipour, Hossein Mehrabi
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Abstract The zwitterions generated from phenanthiridine and dialkyl acetylenedicarboxylates (DAADs) react with a variety of arylidenemalononitriles, affording substituted pyrido[1,2-f]phenanthridines.
Mahdi Hatamipour, Hossein Mehrabi
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