Literature DB >> 23978241

Synthesis of isomeric isothiazolo[4',3':4,5]- and isothiazolo[4',5':4,5]thieno[3,2-b]pyrano[2,3-d]pyridines by combination of domino reactions.

Anatoliy M Shestopalov1, Natalia A Larionova, Alexander E Fedorov, Lyudmila A Rodinovskaya, Valery Yu Mortikov, Andrey A Zubarev, Ivan S Bushmarinov.   

Abstract

Isothiazolothienopyridines have been prepared by a domino reaction (the SN2 reaction → the Thorpe-Ziegler reaction → the Thorpe-Guareschi reaction type) from disodium 4-cyanoisothiazole-3,5-dithiolate. By changing the order of addition of the alkylation reagents in the reaction with disodium 4-cyanoisothiazole-3,5-dithiolate both possible isomers of the isothiazolothienopyridines are synthesized. These isomers were further used in three-component domino reaction (the Knoevenagel reaction → the Michael reaction → the hetero-Thorpe-Ziegler reaction type) to obtain wide range of isomeric isothiazolothienopyranopyridines.

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Year:  2013        PMID: 23978241     DOI: 10.1021/co400066y

Source DB:  PubMed          Journal:  ACS Comb Sci        ISSN: 2156-8944            Impact factor:   3.784


  1 in total

1.  Crystal structure of 8-[7,8-bis-(4-chloro-benzo-yl)-7H-cyclo-penta-[a]ace-naphthylen-9-yl]naphthalene-1-carb-oxy-lic acid.

Authors:  Jomon P Jacob; M Sithambaresan; Christy Kunjachan; M R Prathapachandra Kurup
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-01-01
  1 in total

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