نتایج جستجو برای: tetracyclic graphs

تعداد نتایج: 97937  

Journal: :Tetrahedron letters 2011
Derek Fischer Thong X Nguyen Lynnie Trzoss Marianna Dakanali Emmanuel A Theodorakis

Stabilized 2-amino-1,3-dienes can participate in intramolecular Diels-Alder (IMDA) reactions with pendant dienophiles. We found that these dienes can be readily prepared via standard palladium-mediated coupling reactions and have comparable reactivity to 2-oxodienes. Application of these substrates to the synthesis of tetracyclic model systems representing the ABCE motif of the zoanthamines is ...

Journal: :Angewandte Chemie 2013
Brian N Laforteza Mark Pickworth David W C Macmillan

Dressed to the nines: The first enantioselective total synthesis of (-)-minovincine has been accomplished in nine chemical steps and 13 % overall yield. A novel, one-step Diels-Alder/β-elimination/conjugate addition organocascade sequence allowed rapid access to the central tetracyclic core in an asymmetric manner. Boc=tert-butoxycarbonyl, LG=leaving group, PMB=para-methoxybenzyl.

Journal: :Chemical science 2017
A Kong D E Mancheno N Boudet R Delgado E S Andreansky S B Blakey

The first total synthesis of malagashanine, a chloroquine potentiating indole alkaloid, is presented. A highly stereoselective cascade annulation reaction was developed to generate the tetracyclic core of the Malagasy alkaloids. This chemistry is likely to be broadly applicable to the synthesis of other members of this stereochemically unique family of natural products.

Journal: :Organic letters 2005
Don M Cho Sean R Parkin Mark D Watson

[structure: see text] We report the synthesis and characterization of partially fluorinated condensed tetracyclic aromatic compounds. Typical edge-to-face/herringbone packing of nonfluorinated analogues is replaced here by columnar stacks with disk planes orthogonal to the columnar axes. Enhanced pi-overlap results with overlaid electron-poor and -rich regions.

Journal: :European journal of medicinal chemistry 2012
Carla S Francisco Lígia R Rodrigues Nuno M F S A Cerqueira Ana M F Oliveira-Campos Lígia M Rodrigues

The synthesis of five new tetracyclic benzofurocoumarin (benzopsoralen) analogues is described. Their inhibitory effects on the growth of three human tumor cell lines (MDA MB 231 (breast adenocarcinoma), HeLa (cervix adenocarcinoma) and TCC-SUP (bladder transitional cell carcinoma) were evaluated, and discussed in terms of structure-activity relationship.

2017
Juan Liu Yangrong Xu Jingjing Yang Wenzhi Wang Jianqiang Zhang Renmei Zhang Qingguo Meng

Ocotillol-type saponins are one kind of tetracyclic triterpenoids, sharing a tetrahydrofuran ring. Natural ocotillol-type saponins have been discovered in Panax quinquefolius L., Panax japonicus, Hana mina, and Vietnamese ginseng. In recent years, the semisynthesis of 20(S/R)-ocotillol-type saponins has been reported. The biological activities of ocotillol-type saponins include neuroprotective ...

2012
Piyush Kumar Agarwal Meena Devi Dathi Mohammad Saifuddin Bijoy Kundu

A mild, efficient and versatile method has been developed for the construction of a functionalized natural product, meridianin, and its post conversion to pyrimido-β-carboline by cationic π- cyclization. The strategy involves the introduction of an amino group at the C-5 of the pyrimidine ring and utilizing the nucleophilictiy of the C-2 in the indole ring to facilitate cationic π-cyclization.

Journal: :transactions on combinatorics 2014
alireza abdollahi shahrooz janbaz

let $n$ be any positive integer, the friendship graph $f_n$ consists of $n$ edge-disjoint triangles that all of them meeting in one vertex. a graph $g$ is called cospectral with a graph $h$ if their adjacency matrices have the same eigenvalues. recently in href{http://arxiv.org/pdf/1310.6529v1.pdf}{http://arxiv.org/pdf/1310.6529v1.pdf} it is proved that if $g$ is any graph cospectral with $f_n$...

2013
Fei Zhao Lei Zhang Hailong Liu Shengbin Zhou Hong Liu

An efficient and practical protocol has been developed to synthesize 5,6-dihydroindolo[1,2-a]quinoxaline derivatives by CuI-catalyzed intramolecular N-arylation under microwave irradiation. This method rapidly afforded the tetracyclic products with good to excellent yields (83-97%) in short reaction times (45-60 min).

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