A new, mild one-pot synthesis of iodinated heterocycles as suitable precursors for N-heterocyclic carbene complexes

DSpace/Manakin Repository

Show simple item record

dc.contributor.author Iglesias, Manuel
dc.contributor.author Schuster, Oliver
dc.contributor.author Albrecht, Martin
dc.date.accessioned 2012-06-19T15:41:44Z
dc.date.available 2012-06-19T15:41:44Z
dc.date.copyright 2010 Elsevier en
dc.date.issued 2010-10-13
dc.identifier.citation Tetrahedron Letters en
dc.identifier.uri http://hdl.handle.net/10197/3686
dc.description.abstract The use of I2/AgOAc in dichloromethane constitutes a cheap, mild, and efficient method for the selective iodination of a variety of heterocycles. In a number of cases, this method provides superior yields than other literature methods and affords iodo-functionalized heterocycles that are suitable precursors for carbene complexes. en
dc.description.sponsorship European Research Council en
dc.format.extent 466325 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.publisher Elsevier en
dc.rights This is the author’s version of a work that was accepted for publication in etrahedron Letters. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron Letters (2010) DOI: http://dx.doi.org/10.1016/j.tetlet.2010.07.178 en
dc.subject Iodination en
dc.subject Imidazole en
dc.subject N-heterocyclic carbene en
dc.subject Oxidative addition en
dc.subject Ligand precursors en
dc.subject Abnormal carbene complexes en
dc.subject.lcsh Heterocyclic compounds en
dc.subject.lcsh Imidazoles en
dc.subject.lcsh Carbenes (Methylene compounds) en
dc.title A new, mild one-pot synthesis of iodinated heterocycles as suitable precursors for N-heterocyclic carbene complexes en
dc.type Journal Article en
dc.internal.availability Full text available en
dc.status Peer reviewed en
dc.identifier.volume 51 en
dc.identifier.issue 41 en
dc.identifier.startpage 5423 en
dc.identifier.endpage 5425 en
dc.identifier.doi 10.1016/j.tetlet.2010.07.178
dc.neeo.contributor Iglesias|Manuel|aut| en
dc.neeo.contributor Schuster|Oliver|aut| en
dc.neeo.contributor Albrecht|Martin|aut| en
dc.description.othersponsorship Swiss National Science Foundation FP7 (Marie Curie Action) en


Files in this item

This item appears in the following Collection(s)

Show simple item record

This item is available under the Attribution-NonCommercial-NoDerivs 3.0 Ireland. No item may be reproduced for commercial purposes. For other possible restrictions on use please refer to the publisher's URL where this is made available, or to notes contained in the item itself. Other terms may apply.

If you are a publisher or author and have copyright concerns for any item, please email research.repository@ucd.ie and the item will be withdrawn immediately. The author or person responsible for depositing the article will be contacted within one business day.

Search Research Repository


Advanced Search

Browse