نتایج جستجو برای: chromenes

تعداد نتایج: 289  

Journal: :Chemical Society reviews 2012
Manuel Natali Silvia Giordani

This critical review focuses on the development of photochromic compounds as sensors for cations, anions, and biologically important molecules. The review commences with a brief description of photochromism and the strategies to exploit photochromic molecular switches' properties for sensing application. This is followed by a summary of photoswitchable receptors emerged to date and classified a...

2012
Johannes Reisch Ranjith W. Dharmaratne

2-Dimethyl-2H-Chromenes, Coumarin Derivatives, Phase-Transfer Catalysis 2,2-Dimethyl-5H-pyrano(3,2-c)-l-benzopyrano-5-one(2) and 4H-2,3-dihydro-3-methyl-2methylene-furan-l-benzopyran-4-one (3), two new coumarin derivatives were synthesised from 4-hydroxycoumarin by treating with 3-chloro-3-methylbut-l-yne and 3-chlorobut-l-yne respectively, both reactions progressing via the phase-transfer cata...

2017
Weian Zhang Ziyuan Zhao Zhi Wang Chao Guo Chunyu Wang Rui Zhao Lei Wang Sandrine Bouquillon

Synthesis of indolyl 4H-chromenes via a three-component reaction catalyzed by lipase in ionic liquidsis reported here for the first time. High yields (77–98%) were obtained when Mucor miehei lipase was used as the catalyst in [EMIM][BF4]. Furthermore, [EMIM][BF4] exhibited good reusability in this enzymatic reaction. This study affords a new example of lipase catalytic promiscuity and broadens ...

Journal: :Bulletin of the Chemical Society of Japan 1984

حیدری کشل, سعید , خوش زبان, احد , دیوسالار, کورس , رجبعلیان, سعید , صفوی, ملیحه سادات , فرومدی, علیرضا , محققی, محمدعلی , محمودی, مجید ,

Background: 4-Aryl-4H-chromenes are novel anticancer agents which induce apoptosis in cancer cells. These compounds were found to induce apoptosis by targeting the tubulin/microtubule system in cell proliferation process. The aim of this study was to report cyototoxic and apoptosis inducing activities of a new series of synthesized 4-aryl-4H-chromenes compounds. Methods: The in vitro cytotoxic...

2010
M. Vosooghi S. Rajabalian M. Sorkhi M. Badinloo M. Nakhjiri A.S. Negahbani A. Asadipour M. Mahdavi A. Shafiee A. Foroumadi

A series of 2-amino-4-aryl-3-cyano-7- (dimethylamino)-4H-chromenes was synthesized by condensation of 3- (dimethylamino) phenol, an aromatic aldehyde and malonitrile in ethanol containing piperidine. The assignments of the structure of all synthesized compounds were based on spectral data (IR, Mass and(1)H NMR). The cytotoxic activities of the synthesized compounds against six human tumor cell ...

Journal: :Catalysts 2022

An organocatalytic [4 + 2] cascade annulation of salicylaldehydes and 1,3-bisarylsulfonylpropenes has been developed. This protocol enables the efficient straightforward synthesis a new series 3-sulfonyl-2-sulfonylmethyl-2H-chromenes that are useful for exploring pharmacologically valued compounds. Further reductive modifications result in 3-desulfonylated chromene or chromane derivatives. can ...

Journal: :research in pharmaceutical sciences 0
m vosooghi s rajabalian m sorkhi m badinloo m nakhjiri as negahbani

a series of 2-amino-4-aryl-3-cyano-7-(dimethylamino)-4 h -chromenes was synthesized by condensation of 3-(dimethylamino)phenol, an aromatic aldehyde and malonitrile in ethanol containing piperidine. the assignments of the structure of all synthesized compounds were based on spectral data (ir, mass and 1 h nmr). the cytotoxic activities of the synthesized compounds against six human tumor cell l...

Journal: :Organic & biomolecular chemistry 2015
V Kameswara Rao Pinku Kaswan Keykavous Parang Anil Kumar

In(OTf)3 catalyzed microwave-assisted alkenylation of methoxyphenols was investigated. Exclusive formation of either indenes or chromenes was observed depending on the position of the methoxy group on phenol. The structures of 1H-inden-4-ol derivatives (4a-e) and 4H-chromene derivatives (5a-j) were established by NMR ((1)H & (13)C) and high-resolution mass spectra, which were further supported ...

Journal: :Bioorganic & medicinal chemistry letters 2012
Narender Reddy Emmadi Krishnaiah Atmakur Ganesh Kumar Chityal Sujitha Pombala Jagadeesh Babu Nanubolu

A series of fluorinated tetrahydropyrano[3,2-c]chromenes and dihydropyrano[3,2-b]pyran derivatives have been synthesized and their in vitro cytotoxic activities have been determined in cervical cancer cell line (HeLa), human breast adenocarcinoma cell line (MDA-MB-231 and MCF-7) and human alveolar adenocarcinoma cell line (A549). Compounds 4g, 4k, 4p showed a very potent activity against MDA-MB...

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