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ChemInform Abstract: Dihydro‐1,4‐benzodiazepinones and ‐thiones
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. WALSER, R. I. FRYER
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Variable temperature n.m.r. behaviour of 1,5‐benzodiazepinones and 1,5‐benzodiazepinthiones
AbstractThe n.m.r. variable temperature behaviour of the 7‐membered ring in 1,3‐dihydro‐2H‐1,5‐benzodiazepin‐2‐one derivatives and in the corresponding 2‐thiones has been investigated. The results indicate that the ring inversion barrier is higher in the thiones and dependent on substituents bonded at N‐1.
R. BENASSI +4 more
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A robust and scalable formal [4 + 3] annulation reaction for the synthesis of optically pure 1,4-benzodiazepinones and 1,4-benzoxazepinones has been established by a combined catalytic system consisting of a chiral NHC, a chiral Ir/phosphine-olefin ...
Yang-Yang Li, Zi-Jing Zhang, Jin Song
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Vinyl-substituted 1,4-benzodiazepinones were obtained in good yields (10 examples, 61-82% yield) via the reaction between N-allenyl anthranyl amides and aryl iodides under Pd(0) catalysis.
Micol Rigamonti +2 more
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Opioid analgesics/benzodiazepinones/tetrahydrocannabinol overdose
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Soluble polymer-supported synthesis of benzodiazepinones
Bioorganic & Medicinal Chemistry Letters, 2002Soluble polymer-supported synthetic method provides a highly efficient route for the construction of biologically important 1,5-benzodiazepin-2-ones. A library of N-substituted benzodiazepinones can be readily assembled utilizing S(N)Ar reaction, reduction of nitro group and one-pot cyclization following N-alkylation as the key step in the synthesis ...
Cheng Yi, Wu, Chung Ming, Sun
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On substituent effect on the benzodiazepinone system
Computational and Theoretical Chemistry, 2012Abstract Tautomerism, aromaticity, and electron density at ring critical points of substituted benzodiazepinones, composed of condensed 6- and 7-membered rings (7-substituted 1,3-dihydro-benzo[e][1,4]diazepin-2-ones), were studied at the B3LYP/6-31G ∗∗ level. We found that in the gas phase and in water, the N1H tautomers are more stable than the N4H
Grażyna Karpińska +2 more
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