Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/5057
Title: Reaction of thieno[2,3-b]pyridines with sodium hypochlorite: An unusual and stereoselective one-pot approach to dimeric pyrrolo[2′,3′:4,5]thieno[2,3-b]pyridines
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Keywords: Dimerization;Oxidation;Sodium hypochlorite;Thieno[2,3-b]pyridines
Issue Date: 2019
Publisher: Elsevier Ltd
Citation: Stroganova, T.A., Vasilin, V.K., Dotsenko, V.V., Aksenov, N.A., Krapivin, G.D. Reaction of thieno[2,3-b]pyridines with sodium hypochlorite: An unusual and stereoselective one-pot approach to dimeric pyrrolo[2′,3′:4,5]thieno[2,3-b]pyridines // Tetrahedron Letters. - 2019. - Volume 60. - Issue 14. - Pages 997-1000
Series/Report no.: Tetrahedron Letters
Abstract: The oxidation of 3-aminothieno[2,3-b]pyridine-2-carboxamides with commercially available bleach leads to the formation of dimeric pyrrolo[2′,3′:4,5]thieno[2,3-b]pyridines (7a,14a-diamino-7,14-bis(aryl)-7,7a,14,14a-tetrahydro-6H,13H-pyrido[3″″,2″″:4‴,5‴]thieno[2‴,3‴:4″,5″]pyrrolo-[3″,4″:3′,4′]pyrrolo[2′,3′:4,5]thieno[2,3-b]pyridine-6,13-diones) in moderate yields (37–52%)
URI: http://hdl.handle.net/20.500.12258/5057
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