| Literature DB >> 23978241 |
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.Entities:
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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