Literature DB >> 24634543

Bichalcophenes: A Concise Synthesis of Formyl Ester- and Cyano Ester-Substituted Bithiophenes, Bifurans, and Furanothiophenes.

Abdelbasset A Farahat1, Arvind Kumar2, Alaa El-Din M Barghash3, Fatma E Goda3, Hassan M Eisa3, David W Boykin2.   

Abstract

Syntheses of new formyl ester- and cyano ester-substituted bithiophenes, bifurans, and furanothiophenes in good yield are described. The key synthetic step uses Stille coupling of appropriately substituted bromo 5-ring heterocycles with stannyl-substituted 5-ring heterocycles.

Entities:  

Year:  2010        PMID： 24634543      PMCID： PMC3949757          DOI： 10.1002/jhet.295

Source DB:  PubMed          Journal:  J Heterocycl Chem        ISSN： 0022-152X            Impact factor:   2.193


  11 in total

1.  Structure-specific recognition of quadruplex DNA by organic cations: influence of shape, substituents and charge.

Authors:  Elizabeth W White; Farial Tanious; Mohamed A Ismail; Anthony P Reszka; Stephen Neidle; David W Boykin; W David Wilson
Journal:  Biophys Chem       Date:  2006-06-20       Impact factor: 2.352

2.  Organic dyes containing furan moiety for high-performance dye-sensitized solar cells.

Authors:  Jiann T Lin; Pin-Cheng Chen; Yung-Sheng Yen; Ying-Chan Hsu; Hsien-Hsin Chou; Ming-Chang P Yeh
Journal:  Org Lett       Date:  2009-01-01       Impact factor: 6.005

3.  A light-resistant organic sensitizer for solar-cell applications.

Authors:  Jun-Ho Yum; Daniel P Hagberg; Soo-Jin Moon; Karl Martin Karlsson; Tannia Marinado; Licheng Sun; Anders Hagfeldt; Mohammad K Nazeeruddin; Michael Grätzel
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

4.  Detection of arsenical drug resistance in Trypanosoma brucei with a simple fluorescence test.

Authors:  Mhairi L Stewart; Sanjeev Krishna; Richard J S Burchmore; Reto Brun; Harry P de Koning; David W Boykin; Richard R Tidwell; J Ed Hall; Michael P Barrett
Journal:  Lancet       Date:  2005 Aug 6-12       Impact factor: 79.321

5.  Screening for and identification of novel agents directed at renal cell carcinoma.

Authors:  S D Mertins; T G Myers; M Hollingshead; D Dykes; E Bodde; P Tsai; C A Jefferis; R Gupta; W M Linehan; M Alley; S E Bates
Journal:  Clin Cancer Res       Date:  2001-03       Impact factor: 12.531

6.  Inhibition of Src kinase activity by 7-[(2,4-dichloro-5-methoxyphenyl)amino]-2-heteroaryl-thieno[3,2-b]pyridine-6-carbonitriles.

Authors:  Diane H Boschelli; Biqi Wu; Ana Carolina Barrios Sosa; Joan J Chen; Jennifer M Golas; Frank Boschelli
Journal:  Bioorg Med Chem Lett       Date:  2005-11-01       Impact factor: 2.823

7.  Carbon dioxide induced phase switching for homogeneous-catalyst recycling.

Authors:  Simon L Desset; David J Cole-Hamilton
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

8.  Amino(oligo)thiophene-based environmentally sensitive biomembrane chromophores.

Authors:  Ping Yan; Aifang Xie; Meide Wei; Leslie M Loew
Journal:  J Org Chem       Date:  2008-07-30       Impact factor: 4.354

9.  Amidine catalysed O- to C-carboxyl transfer of heterocyclic carbonate derivatives.

Authors:  Caroline Joannesse; Carmen Simal; Carmen Concellón; Jennifer E Thomson; Craig D Campbell; Alexandra M Z Slawin; Andrew D Smith
Journal:  Org Biomol Chem       Date:  2008-06-16       Impact factor: 3.876

10.  Thienopyrimidine-based dual EGFR/ErbB-2 inhibitors.

Authors:  Tara R Rheault; Thomas R Caferro; Scott H Dickerson; Kelly H Donaldson; Michael D Gaul; Aaron S Goetz; Robert J Mullin; Octerloney B McDonald; Kimberly G Petrov; David W Rusnak; Lisa M Shewchuk; Glenn M Spehar; Anne T Truesdale; Dana E Vanderwall; Edgar R Wood; David E Uehling
Journal:  Bioorg Med Chem Lett       Date:  2008-12-07       Impact factor: 2.823
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  1 in total

1.  Indole and Benzimidazole Bichalcophenes: Synthesis, DNA Binding and Antiparasitic Activity.

Authors:  Abdelbasset A Farahat; Mohamed A Ismail; Arvind Kumar; Tanja Wenzler; Reto Brun; Ananya Paul; W David Wilson; David W Boykin
Journal:  Eur J Med Chem       Date:  2017-10-22       Impact factor: 6.514
  1 in total

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