Results 201 to 210 of about 5,260 (223)
Some of the next articles are maybe not open access.
Conversion of tetrahydroisoquinolinium salts into benzazepines
The Journal of Organic Chemistry, 1984Conversion de methyl-2 nitro-4' benzyl-2 tetrahydro-1,2,3,4 isoquinoleiniums en methyl-3 nitro-4' phenyl-2 tetrahydro-2,3,4,5 benzoazepines-3 par action du t-butanolate de potassium dans le t-butanol.
Stephen Smith +2 more
openaire +1 more source
A New Synthesis of 2-Benzazepines
Synthesis, 2002AlCl 3 -mediated intramolecular cyclization of N,N-bis(1H-1,2,3-benzotriazol-1-ylmethyl)-3-phenyl-1-propanamine (5) gave 2-benzotriazolylmethyl-2,3,4,5-tetrahydro-1H-2-benzazepine (6). Subsequent nuclcophilic substitution of the benzotriazolyl group in 6 with Grignard reagents, triethyl phosphite and sodium borohydride afforded 2,3,4,5-tetrahydro-1H-2 ...
Alan R. Katritzky +3 more
openaire +1 more source
Chemischer Informationsdienst, 1986
AbstractTreatment of laevulinic acid (I) with the anilines (II) and its salts (III) yields the benzazepinones (IV).
J. H. BOWIE +7 more
openaire +1 more source
AbstractTreatment of laevulinic acid (I) with the anilines (II) and its salts (III) yields the benzazepinones (IV).
J. H. BOWIE +7 more
openaire +1 more source
Chemischer Informationsdienst, 1982
AbstractTetrahydrobenzazepinon (VI) wird durch die angegebene Reaktionsfolge aus Dihydroisocumarin (I) hergestellt.
openaire +1 more source
AbstractTetrahydrobenzazepinon (VI) wird durch die angegebene Reaktionsfolge aus Dihydroisocumarin (I) hergestellt.
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source
International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology, 1990
Walte Burger +2 more
openaire +1 more source
Walte Burger +2 more
openaire +1 more source
Gold-Catalyzed Synthesis of Benzazepines
Synfacts, 2009J. Pérez-Castells +2 more
openaire +1 more source

