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Chemischer Informationsdienst, 1982
AbstractTetrahydrobenzazepinon (VI) wird durch die angegebene Reaktionsfolge aus Dihydroisocumarin (I) hergestellt.
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AbstractTetrahydrobenzazepinon (VI) wird durch die angegebene Reaktionsfolge aus Dihydroisocumarin (I) hergestellt.
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Benzazepin‐Derivate aus 2‐Äthoxy‐indol
Chemische Berichte, 1966AbstractBei der Reaktion von 2‐Äthoxy‐indol mit Acetylendicarbonsäure‐dimethylester wird neben 1 und 2 das Benzazepin‐Derivat 3 gebildet. Ausgehend von 2‐Äthoxy‐1‐methyl‐indol entsteht 4 als einziges faßbares Produkt.
Hans Plieninger, Dieter Wild
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1974
Publisher Summary This chapter discusses 1-, 2-, and 3-Benzazepines. Ring closure with the formation of a carbon-nitrogen bond, of the types A-E shown in the chapter, has been used to synthesize derivatives of 1-, 2-, and 3-benzazepines, with aminocarboxylic acids, amino halides, dihalides, dinitriles, dicarboxylic acids, and carboxylic acid diamides
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Publisher Summary This chapter discusses 1-, 2-, and 3-Benzazepines. Ring closure with the formation of a carbon-nitrogen bond, of the types A-E shown in the chapter, has been used to synthesize derivatives of 1-, 2-, and 3-benzazepines, with aminocarboxylic acids, amino halides, dihalides, dinitriles, dicarboxylic acids, and carboxylic acid diamides
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International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology, 1990
Walte Burger +2 more
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Walte Burger +2 more
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Gold-Catalyzed Synthesis of Benzazepines
Synfacts, 2009J. Pérez-Castells +2 more
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