Results 91 to 100 of about 607 (146)

The synthesis and energy barriers to ring inversion of triazolo[4,3-d][1,4]benzodiazepinones

, 1976
M.S. Puar, P.C. Wade, B.R. Vogt
core   +1 more source

ChemInform Abstract: Studies Related to Alkylations of Enolate Anions of 1,4- Benzodiazepinones.

, 2010
R. I. FRYER, R. B. UPASANI, J. C. PINTO
core   +1 more source

Stereoselective [4+3]-Cycloaddition of 2-Amino-β-nitrostyrenes with Azaoxyallyl Cations to Access Functionalized 1,4-Benzodiazepin-3-ones. [PDF]

Molecules
Kim Y, Kim SG.
europepmc   +1 more source

1,3-Dipolar Cycloaddition−Decarboxylation Reactions of an Azomethine Ylide with Isatoic Anhydrides: Formation of Novel Benzodiazepinones

, 2011
Nadia Spiccia, Jose Basutto, Jonathan M. White, Pawel Jokisz, Andrew B. Holmes, John H. Ryan, Adam G. Meyer, Leon S.-M. Wong   +7 more
core   +1 more source

ChemInform Abstract: Synthesis and Biological Activity of N‐Substituted 2,3,4,5‐Tetrahydro‐1H‐1,5‐benzodiazepinones‐2.

, 1986
B. A. PUODZHYUNAITE, YU. M. RABOTNIKOV, Z. A. TALAIKITE, R. A. YANCHENE, A. S. ZAKS, E. A. USACHEV   +5 more
core   +1 more source

Asymmetric Ir-catalyzed hydrogenation of 1,5-benzodiazepinones using mixtures of ligands

, 2017
S. E. Lyubimov, V. A. Davankov, D. V. Ozolin   +2 more
core   +1 more source

Klebsiella oxytoca inhibits Salmonella infection through multiple microbiota-context-dependent mechanisms. [PDF]

Nat Microbiol
Osbelt L, Almási ÉDH, Wende M, Kienesberger S, Voltz A, Lesker TR, Muthukumarasamy U, Knischewski N, Nordmann E, Bielecka AA, Giralt-Zúñiga M, Kaganovitch E, Kühne C, Baier C, Pietsch M, Müsken M, Greweling-Pils MC, Breinbauer R, Flieger A, Schlüter D, Müller R, Erhardt M, Zechner EL, Strowig T.   +23 more
europepmc   +1 more source

Iridium Catalyzed Asymmetric Hydrogenation of Cyclic Imines of Benzodiazepinones and Benzodiazepines

Organic Letters, 2012
Highly enantioselective Ir-catalyzed hydrogenation of seven-membered cyclic imines of benzodiazepinones and benzodiazepines was achieved with up to 96% ee. This method provides a direct access to synthesize a range of chiral cyclic amines existing in numerous important natural products and clinical drugs.
Kai Gao, Chang-Bin Yu, Qing-An Chen
exaly   +4 more sources

First Highly Enantioselective Synthesis of Benzodiazepinones by Catalytic Hydrogenation

Advanced Synthesis and Catalysis, 2010
AbstractThe first catalytic enantioselective synthesis of benzodiazepinones employing an efficient hydrogenation protocol has been developed. The corresponding products are obtained in good yields, with excellent enantioselectivities and broad functional group tolerance.
Magnus Rueping, Estibaliz Merino, René M Koenigs   +2 more
exaly   +3 more sources

Some of the next articles are maybe not open access.

Related searches:

A new route to 1H-1,5-benzodiazepinones

Journal of the Chemical Society Chemical Communications, 1981
Dimethyl allene-1,3-dicarboxylates react with o-phenylenediamine to give 1H-1, 5-benzodiazepinones and not benzimidazoles; the transient enamine intermediate shows preference for a 7-exo-trig ring closure.
Feodor Scheinmann
exaly   +3 more sources