Results 31 to 40 of about 76 (75)
P-5227: an active dibenzoxepine antipsychotic.
A A, Sugerman, F J, Lichtigfeld
openaire +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Recent Advances on the Development of Synthetic Strategies to Access Dibenzoxepine Derivatives
Synthesis, 2022AbstractDibenzoxepines have gained privileged status in medicinal chemistry and drug discovery due to their appearance in various natural products and life-saving drug molecules. Dibenzoxepine-based molecules, such as artocarpols, asenapine, and pacharin, possess a wide range of biological activities including anti-inflammatory, antidepressant ...
Surisetti Suresh +2 more
openaire +1 more source
Synthesis of antimicrotubule dibenzoxepines
Tetrahedron Letters, 2010Abstract New dibenzoxepines 5a–i bearing various substituents on B- and C-rings were synthesized in a straightforward manner using a Suzuki–Miyaura coupling, a Grignard addition, and a cyclodehydration as key steps. The antimicrotubule activity of all analogues was evaluated and compared to reference compounds.
Colombel, V. +6 more
openaire +2 more sources
Dibenzoxepines as treatments for neurodegenerative diseases
Pure and Applied Chemistry, 1999Abstract
Kaspar Zimmermann +2 more
openaire +1 more source
Organic & Biomolecular Chemistry, 2021
DAST-mediated intramolecular Friedel–Crafts cyclization is developed for the synthesis of novel spirooxindoles fused with dibenzoxepine moieties.
Ramesh Samikannu +10 more
openaire +2 more sources
DAST-mediated intramolecular Friedel–Crafts cyclization is developed for the synthesis of novel spirooxindoles fused with dibenzoxepine moieties.
Ramesh Samikannu +10 more
openaire +2 more sources
Applied Organometallic Chemistry, 2021
AbstractFrom the past decade so far, the synthesis of seven‐membered oxacycles especially natural monocyclic oxepines and their annulated derivatives has received considerable attention. Due to the importance of these valuable scaffolds in natural products, pharmaceuticals, and prospective drugs, as well as their strong potential for use in the ...
Fatemeh Rafiee, Samira Hasani
openaire +1 more source
AbstractFrom the past decade so far, the synthesis of seven‐membered oxacycles especially natural monocyclic oxepines and their annulated derivatives has received considerable attention. Due to the importance of these valuable scaffolds in natural products, pharmaceuticals, and prospective drugs, as well as their strong potential for use in the ...
Fatemeh Rafiee, Samira Hasani
openaire +1 more source
A Synthetic Route to (±)-Clavizepine through a Dibenzoxepine Intermediate
The Journal of Organic Chemistry, 1996A new synthesis of (±)-clavizepine (1a), based on the dibenzoxepinediol 10 as main intermediate is described. The key step is the contraction of the oxepine ring to give the xanthene-9-carboxyaldehyde 11, on which the nitrogenated ring can be readily assembled.
M. C. de la Fuente +2 more
openaire +1 more source
The synthesis of pacharin: a dibenzoxepine from the heartwood of Bauhinia racemosa Lamk.
Journal of the Chemical Society, Perkin Transactions 1, 1990The synthesis of the novel dibenzoxepine derivative pacharin (13)(8-methoxy-7-methyldibenz[b,f]-oxepine-1,6-diol), a constituent of the heartwood of Bauhinia racemosa Lamk., is described The route depended on the formation of the diphenyl ether (8) which was converted by standard synthetic steps into the bisphosphonium salt (11).
Mark F. Comber, Melvyn V. Sargent
openaire +1 more source
Total synthesis of cularine alkaloids via dibenzoxepines as key intermediates
Tetrahedron, 1995Abstract The total synthesis of several cularine alkaloids (cularine, oxocularine, dioxocularine and 4-hydroxycularine) via 10,11-dihydrodibenz(b,f)oxepin-10-ones as key intermediates is reported.
Alberto Garcia +2 more
openaire +1 more source
ChemInform Abstract: A Synthetic Route to (.+‐.)‐Clavizepine Through a Dibenzoxepine Intermediate.
ChemInform, 1997AbstractChemInform 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.
M. C. DE LA FUENTE +2 more
openaire +1 more source

