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<dc:title>A Practical, One-Pot Synthesis of Highly Substituted Thiophenes and Benzo[b]thiophenes from Bromoenynes and o-Alkynylbromobenzenes</dc:title>
<dc:creator>Guilarte Moreno, Verónica</dc:creator>
<dc:creator>Fernández Rodríguez, Manuel A.</dc:creator>
<dc:creator>García García, Patricia</dc:creator>
<dc:creator>Hernando Santa Cruz, Elsa</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:subject>Química orgánica</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:subject>Chemistry, Organic</dc:subject>
<dc:description>An efficient synthesis of thiophenes and benzo[b]thiophenes has been developed from easily available bromoenynes and o-alkynylbromobenzene derivatives. This novel one-pot procedure involves a Pd-catalyzed C–S bond formation using a hydrogen sulfide surrogate followed by a heterocyclization reaction. Moreover, in situ functionalization with selected electrophiles further expands the potential of this methodology to the preparation of the corresponding highly substituted sulfur heterocycles.</dc:description>
<dc:description>Junta de Castilla y Leon (BU021A09 and GR-172) and Ministerio de Ciencia e Innovacion (MICINN) and FEDER (CTQ2010-15358 and CTQ2009-09949/BQU) for financial support. P.G.-G. and M.A.F.-R. thank MICINN for "Juan de la Cierva" and "Ramon y Cajal" contracts</dc:description>
<dc:description>Junta de Castilla y Leon (BU021A09 and GR-172) and Ministerio de Ciencia e Innovacion (MICINN) and FEDER (CTQ2010-15358 and CTQ2009-09949/BQU) for financial support. P.G.-G. and M.A.F.-R. thank MICINN for "Juan de la Cierva" and "Ramon y Cajal" contracts</dc:description>
<dc:description>This document is the Accepted Manuscript version of a Published Work that appeared in final form in&#xd;
Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher.</dc:description>
<dc:date>2016-01-21T09:51:47Z</dc:date>
<dc:date>2016-01-21T09:51:47Z</dc:date>
<dc:date>2011-09</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
<dc:identifier>1523-7060</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/3909</dc:identifier>
<dc:identifier>10.1021/ol201970m</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Organic Letters. 2011. V. 13, n. 19, p. 5100-5103</dc:relation>
<dc:relation>http://dx.doi.org/10.1021/ol201970m</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2010-15358</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MICINN/CTQ2009-09949/BQU</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU021A09</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/GR-172</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>American Chemical Society</dc:publisher>
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