نتایج جستجو برای: heterocyclic compounds

تعداد نتایج: 232222  

Journal: :Organic letters 2015
Santhivardhana Reddy Yetra Santigopal Mondal Eringathodi Suresh Akkattu T Biju

The N-heterocyclic carbene (NHC)-organocatalyzed enantioselective annulation reaction of pyrazolones with α,β-unsaturated aldehydes proceeding via the chiral α,β-unsaturated acyl azolium intermediates under oxidative conditions is presented. The reaction afforded dihydropyranone-fused pyrazoles in moderate to good yields and good er values under operationally simple and base-free conditions.

Journal: :Acta pharmaceutica 2010
Hayam H Sayed Hebat-Allah S Abbas Eman M H Morsi Abd El-Galil E Amr Nayera A M Abdelwahad

3-Amino-5-(4-chlorophenylamino)-4-cyanofuran-2-carboxamide (2) was used as the key molecule for preparation of various furopyrimidines 3-9 and formation of spiro-cycloalkane furopyrimidines 10, 11. Also, poly fused heterocyclic compounds 13-17 were prepared from compound 2. The synthesized compounds were screened for their antimicrobial activity.

Journal: :iranian journal of pharmaceutical research 0
shima h. m. ebrahim ketabforoosh department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran 14176, iran. mohsen amini department of medicinal chemistry, faculty of pharmacy and drug design and development research center, tehran university of medical sciences, tehran 14176, iran. mohsen vosooghi department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran 14176, iran. abbas shafiee department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran 14176, iran. ebrahim azizi molecular research laboratory, department of pharmacology and toxicology, faculty of pharmacy, medical sciences, university of tehran, tehran, iran. farzad kobarfard department of medicinal chemistry, shahid beheshti school of pharmacy, tehran, iran.

caffeic acid phenethyl ester(cape) suppresses the growth of transformed cells such as human breast cancer cells, hepatocarcinoma , myeloid leukemia, colorectal cancer cells, fibrosarcoma, glioma and melanoma. a group of heterocyclic esters of caffeic acid was synthesized using mitsunobu reaction and the esters were subjected to further structural modification by electrooxidation of the catechol...

In the present research, silica bonded n-propyl-1,3,5-triazine-2,4,6-triamine (SPTT) was synthesized by direct incorporation of chloropropyl groups through co-condensation of tetraethyl orthosilicate (TEOS) and 3-chloropropyl trimethoxysilane (CPTMS) and subsequent grafting the melamine onto the propyl groups via simple nucleophilic substitution reaction. The catalyst has been characterized by ...

Journal: :Bulletin of the Chemical Society of Japan 1957

2010
Vikas Sharma Pradeep Kumar Devender Pathak

Heterocyclic compounds are those cyclic compounds in which one or more of the ring carbons are replaced by another atom. The non-carbon atoms in such rings are referred to as ‘‘heteroatoms.’’ Such bicyclic heterocyclic compounds containing pyrrole ring with benzene ring fused to a,b-position are known as Indoles. Indole has a benzene ring and pyrrole ring sharing one double bond. It is a hetero...

2011
Geeta Mishra Arvind K. Singh Kshtiz Jyoti

Abstract: Heterocyclic compounds occupy a central position among those molecule that makes life possible. The chemistry of heterocyclic compounds has been an interesting field of study for a long time. Heterocyclic nucleus 1,3,4thiadiazole constitutes constitutes an important class of compounds for new drug development. The synthesis of novel thiadiazole derivatives and investigation of their c...

2015
Hengshuai Wang Shengchao Jiao Kerong Chen Xu Zhang Linxiang Zhao Dan Liu Yu Zhou Hong Liu

We report a synthetic methodology for the construction of the fused heterocyclic compounds pyrido[2,1-b]quinazolin-9(1H)-ones and pyrrolo[2,1-b]quinazolin-9(1H)-ones through an AgOTf-catalyzed intramolecular alkyne hydroamination reaction. The methodology is applicable to a wide scope of substrates and produces a series of fused quinazolinone heterocycles in good to excellent yields.

2008
Sajid Ali Aurangzeb Hasan Nasim Hasan Rama Amir Badshah Ales Ruczika

The title compound, C(12)H(14)O(4), is an important inter-mediate in the synthesis of biologically active heterocyclic compounds. In the crystal structure, inter-molecular O-H⋯O and C-H⋯O hydrogen bonds link the mol-ecules. There are also C-H⋯π contacts between the benzene ring and the methyl-ene groups.

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