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Synthesis 2013; 45(14): 1975-1982
DOI: 10.1055/s-0033-1338481
DOI: 10.1055/s-0033-1338481
paper
Electrophilic Cyclization of o-Anisole- and o-Thioanisole-Substituted Ynamides: Synthesis of 2-Amidobenzofurans and 2-Amidobenzothiophenes
Further Information
Publication History
Received: 25 March 2013
Accepted after revision: 24 April 2013
Publication Date:
15 May 2013 (online)
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Abstract
A facile synthesis of 3-substituted 2-amidobenzofurans and 2-amidobenzothiophenes via electrophilic cyclization reaction of o-anisole- and o-thioanisole-substituted ynamides with I2, NBS and NCS was developed. The products 3-iodo-2-amidobenzofurans were further transferred into 3-aryl-, 3-alkynyl, and 3-vinyl-2-amidobenzofurans via Pd-catalyzed reactions such as Suzuki–Miyaura and Sonogashira cross-coupling reactions and the Heck reaction.
Key words
2-amidobenzofurans - 2-amidobenzothiophenes - electrophilic cyclization - ynamide - cross-coupling reactionSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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For electrophilic cyclization chemistry, see:
For the synthesis of 2-amidobenzofurans, see:
For the synthesis of ynamides, see:
For recent reports on the reactions of ynamides, see: