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The Synthesis of Benzazepines via Sequential [3 + 2]-Annulation and [3,3]-Sigmatropic Rearrangement.
Organic LettersA novel annulation reaction of prop-2-ynylsulfonium salts with sulfur ylides and nitrosobenzenes has been developed, affording various benzazepines in moderate to good yields.
Fang Luo+8 more
semanticscholar +1 more source
Organic Letters
Herein, we report a simple method for the synthesis of 3-benzazepine derivatives via a cobalt-catalyzed, picolinamide-directed α-amidoacrylate C(sp2)-H bond functionalization approach.
Aleksandrs Cizikovs+2 more
semanticscholar +1 more source
Herein, we report a simple method for the synthesis of 3-benzazepine derivatives via a cobalt-catalyzed, picolinamide-directed α-amidoacrylate C(sp2)-H bond functionalization approach.
Aleksandrs Cizikovs+2 more
semanticscholar +1 more source
Organic Letters, 2019
Phosphine-catalyzed divergent [4+3] domino annulations of fluorinated imidoyl chlorides with MBH carbonates were developed. Two classes of perfluoroalkylated benzazepines were obtained in moderate to good yields via an interesting dearomatization ...
Jun-Hua Chen, Zhongmo Yin, You Huang
semanticscholar +1 more source
Phosphine-catalyzed divergent [4+3] domino annulations of fluorinated imidoyl chlorides with MBH carbonates were developed. Two classes of perfluoroalkylated benzazepines were obtained in moderate to good yields via an interesting dearomatization ...
Jun-Hua Chen, Zhongmo Yin, You Huang
semanticscholar +1 more source
1-Benzazepines. The Synthesis and Reactivity of 2-Chloro-1,5-Dimethyl-1h-1-Benzazepines
Australian Journal of Chemistry, 1986Treatment of laevulinic acid with N- methylaniline yields 1,5-dimethyl- 1H-1-benzazepin-2(3H)-one and 5-methyl-5-[4-( methylamino )phenyl]-1- phenylpyrrolidin-2-one. The structure of the latter is confirmed by a single-crystal X-ray study. The yield of benzazepinone is increased if either m- methoxy-N-methylaniline or m-methyl-N- methylaniline is ...
S. Mitkas+7 more
openaire +3 more sources
Journal of Medicinal Chemistry, 1983
A series of 5H-pyrimido[5,4-d][2]benzazepines has been synthesized, starting from the corresponding 2-benzazepin-5-ones, and evaluated as potential anxiolytic agents. Selected compounds from this series show a pharmacological profile of action different than that of diazepam. They are more potent than diazepam in the anti-pentylenetetrazole test and in
J. Sepinwall+9 more
openaire +3 more sources
A series of 5H-pyrimido[5,4-d][2]benzazepines has been synthesized, starting from the corresponding 2-benzazepin-5-ones, and evaluated as potential anxiolytic agents. Selected compounds from this series show a pharmacological profile of action different than that of diazepam. They are more potent than diazepam in the anti-pentylenetetrazole test and in
J. Sepinwall+9 more
openaire +3 more sources
Synthesis of Ring-Fused 1-Benzazepines via [1,5]-Hydride Shift/7-Endo Cyclization Sequences.
Organic Letters, 2017Synthesis of 1-benzazepines has been achieved via a [1,5]-hydride shift/7-endo cyclization sequence. The focus of this research is a direct transformation of 2-(aryl)cyclopropane 1,1-diester derivatives into 1-benzazepines using a cyclopropane moiety as ...
Chang Won Suh, Su Jin Kwon, D. Kim
semanticscholar +1 more source
ChemInform, 1987
AbstractThe benzazepines (II), prepared from the acetylenes (I), are transformed into the isomeric esters (VI) and (VII) by consecutive bromination, dehydrobromination, and palladium‐catalyzed alkoxycarbonylation.
L. Todaro+4 more
openaire +2 more sources
AbstractThe benzazepines (II), prepared from the acetylenes (I), are transformed into the isomeric esters (VI) and (VII) by consecutive bromination, dehydrobromination, and palladium‐catalyzed alkoxycarbonylation.
L. Todaro+4 more
openaire +2 more sources
Journal of Organic Chemistry
A cascade reaction of Pd(II)/dppben-catalyzed [3 + 2] cycloaddition of N-aryl nitrones with allenoates and sequential reduction has been developed for the synthesis of functionalized benzazepines bearing three contiguous carbon stereocenters in moderate ...
Su-Ge Xin+6 more
semanticscholar +1 more source
A cascade reaction of Pd(II)/dppben-catalyzed [3 + 2] cycloaddition of N-aryl nitrones with allenoates and sequential reduction has been developed for the synthesis of functionalized benzazepines bearing three contiguous carbon stereocenters in moderate ...
Su-Ge Xin+6 more
semanticscholar +1 more source
Synthesis and Biological Evaluation of Benzazepine Oxazolidinone Antibacterials.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Betty H. Yagi+8 more
openaire +4 more sources
Synthesis of Spiro[benzazepine-2,4‘-piperidine]
The Journal of Organic Chemistry, 1998AbstractChemInform 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.
D. Gomez Pardo+4 more
openaire +3 more sources