Results 231 to 240 of about 16,503 (251)
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ChemInform Abstract: Remote Activation of the Nucleophilicity of Isatin.
ChemInform, 2014AbstractMichael addition of the isatin imine (I) to aliphatic 1,4‐ketoesters requires a much longer reaction time than the one to aromatic 1,4‐ketoesters.
Margus Lopp +4 more
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Anodic Methoxylation of Isatin
Zeitschrift für Naturforschung B, 1998Abstract Anodic metoxylation of isatin was investigated. The product formed contained a unique 3a.7a-dihydroindole ring system. 3a,7a-Dihydro-(Z)-3a,7a-dimetoxyisatin was isolated and characterized with a variety of spectroscopic methods.
Zygmunt Kazimierczuk +3 more
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Isomerism of isatin-?-aroylhydrazones
Chemistry of Heterocyclic Compounds, 1971The reaction of isatin O-methyl ether with hydrazides of aromatic acids gives the cis and trans forms of α-aroylhydrazones.
P. S. Pel'kis, V. S. Dmitrukha
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Reaction of Isatin with Thiocarbohydrazide: A Correction
Archiv der Pharmazie, 1991AbstractHeterocycles containing the indole ring system include some novel pharmacologically active compounds1–3). Isatin and its N‐acetylisatin are extremely versatile intermediates in the construction of a variety of heterocyclic systems when reacted with thiosemicarbazide derivatives.
M. A. Badawy, Sayed A. Abdel-Hady
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Russian Journal of Organic Chemistry, 2009
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.
A. A. Avetisyan, E. G. Mesropyan
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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.
A. A. Avetisyan, E. G. Mesropyan
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Substituierte Isatin‐phenylimine
Archiv der Pharmazie, 1975Abstract5‐Brom‐ und 5‐Nitro‐isatin kondensieren mit substituierten Anilinen zu Isatin‐3‐(phenyl)‐iminen. 5‐Brom‐isatin‐3‐(phenyl und naphthyl)‐imin werden auch durch Bromieren von Isatin‐3‐(phenyl und naphthyl)‐imin erhalten. Bei Einsatz von o‐Phenylendiamin erfolgt Ringschluß zu 5‐Brom‐bzw.
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430. The structure of isatin and substituted isatins
Journal of the Chemical Society (Resumed), 1956D. G. O'sullivan, P. W. Sadler
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Alkoxyaryloxyketones and their Condensation with Isatins
Journal of the American Chemical Society, 1948Paul K. Calaway, R. L. Sublett
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Asymmetric Addition to Isatins [PDF]
Synfacts, 2010 Tamio Hayashi, R. Shintani, K. Takatsu
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