Results 131 to 140 of about 487 (160)
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A Novel Heterocyclic System: Benzo[b]furo[4,3,2‐ef][1]benzoxepin.

ChemInform, 2005
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A. N. Yamskov   +2 more
openaire   +1 more source

La(OTf)3‐Mediated [3+3]‐Annulation of Benzoxepines and Aminocrotonates: Easy Access to Bridged Bicyclic Benzoxepine Heterocycles†

European Journal of Organic Chemistry
AbstractA new and effective method for making bridged bicyclic benzoxepine derivatives were devised through the intermolecular [3+3]‐annulation of benzoxepine‐3‐carboxylates with aminocrotonates in the presence of La(OTf)3. The compounds were formed through reactions involving the benzoxepine moiety's C‐3 and C‐5 carbons to produce C−C and C−N bonds ...
Sai Teja Kolla   +3 more
openaire   +1 more source

ChemInform Abstract: An Efficient Approach for the Construction of Benzazepine and Benzoxepine Derivatives.

ChemInform, 2013
AbstractThe reaction of 2‐(2‐ethynylphenyl)‐1‐tosylaziridines with various sulfonyl azides affords the corresponding benzazepines with different substitution on the aromatic ring and tolerates various sulfonyl groups [cf.
Shaoyu Li, Shaowu Zou, Jie Wu
openaire   +1 more source

Chemo- and stereoselective synthesis of benzocycloheptene and 1-benzoxepin derivatives as α-sympathomimetic and anorexigenic agents

Bioorganic & Medicinal Chemistry Letters, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Vishnu K, Tandon   +5 more
openaire   +2 more sources

Benzoxepin derivatives: design, synthesis, and pharmacological evaluation with sedative–hypnotic effect

Medicinal Chemistry Research, 2011
A series of novel benzoxepin-derived compounds were synthesized and evaluated for their sedative–hypnotic effect using Phenobarbital-induced sleep test in mice. Compound 6 in which the Phenobarbital moiety was incorporated into the benzoxepin nucleus was the most active one.
Nagwa M. Abdel Gawad   +3 more
openaire   +1 more source

[Pseudotumoral uterine reaction in the rat treated with a benzofuro-benzoxepin].

Comptes rendus des seances de l'Academie des sciences. Serie D, Sciences naturelles, 1981
When orally administered, 5-(3-diméthylamino propyliden)-benzofuro [2,3-c] benzoxepin-1, which antagonizes several biogenic amines, is slightly sedative and has also endocrinological properties in the Rat, induces the appearance of localized lesions of uterine stroma in 2 to 16% of the animals. The cytological picture could suggest a tumorogenesis.
G, Barchewitz   +3 more
openaire   +1 more source

3‐Benzoxepin

Angewandte Chemie, 1961
K. Dimroth, G. Pohl
openaire   +1 more source

A Brief Overview on Chemistry and Biology of Benzoxepine

Letters in Drug Design & Discovery, 2017
Naveen Kuntala   +3 more
openaire   +1 more source

1,6-Oxido [10]annulene and 1-Benzoxepin

Journal of the American Chemical Society, 1964
Franz. Sondheimer, Arnon. Shani
openaire   +1 more source

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