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Department of Organic Chemistry, University of Plovdiv Paisii Hilendarski, 24 Tsar Asen Str., 4000 Plovdiv, Bulgaria
Author to whom correspondence should be addressed.
Academic Editor: Oleg A. Rakitin
Molbank 2021, 2021(2), M1236;
Received: 25 May 2021 / Revised: 8 June 2021 / Accepted: 9 June 2021 / Published: 13 June 2021
(This article belongs to the Section Organic Synthesis)
An convenient one-pot approach for the synthesis of new (E)-2-(2-oxo-4-phenylbut-3-en-1-yl)benzo[d]thiazole-3(2H)-carboxylates is demonstrated. The method is based on a three-component reaction of benzylideneacetone with electrophilic N-alkoxycarbonylbenzothiazolium species formed in situ. The newly synthesized compounds were fully characterized by 1D 1H, 13C- NMR, IR and MS. View Full-Text
Keywords: benzothiazole; benzylideneacetone; α-amidoalkylation; multicomponent reaction benzothiazole; benzylideneacetone; α-amidoalkylation; multicomponent reaction
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MDPI and ACS Style

Stremski, Y.; Statkova-Abeghe, S. (E)-2-(2-Oxo-4-phenylbut-3-en-1-yl)benzo[d]thiazole-3(2H)-carboxylates. Molbank 2021, 2021, M1236.

AMA Style

Stremski Y, Statkova-Abeghe S. (E)-2-(2-Oxo-4-phenylbut-3-en-1-yl)benzo[d]thiazole-3(2H)-carboxylates. Molbank. 2021; 2021(2):M1236.

Chicago/Turabian Style

Stremski, Yordan, and Stela Statkova-Abeghe. 2021. "(E)-2-(2-Oxo-4-phenylbut-3-en-1-yl)benzo[d]thiazole-3(2H)-carboxylates" Molbank 2021, no. 2: M1236.

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