Macrocycle Synthesis by Chloride-Templated Amide Bond Formation
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Otros documentos de la autoría: Martí-Centelles, Vicente; Burguete, M. Isabel; Luis, Santiago V.
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Título
Macrocycle Synthesis by Chloride-Templated Amide Bond FormationFecha de publicación
2016Editor
American Chemical SocietyISSN
0022-3263; 1520-6904Cita bibliográfica
MARTÍ-CENTELLES, Vicente; BURGUETE, Maria Isabel; LUIS, Santiago Vicente. Macrocycle Synthesis by Chloride Templated Amide Bond Formation. The Journal of Organic Chemistry, 2016.Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://pubs.acs.org/doi/abs/10.1021/acs.joc.5b02676Resumen
A new family of pseudopeptidic macrocyclic
compounds has been prepared involving an anion-templated
amide bond formation reaction at the macrocyclization step.
Chloride anion was found to be the most efficient ... [+]
A new family of pseudopeptidic macrocyclic
compounds has been prepared involving an anion-templated
amide bond formation reaction at the macrocyclization step.
Chloride anion was found to be the most efficient template in
the macrocyclization process, producing improved macrocyclization
yields with regard to the nontemplated reaction.
The data suggest a kinetic effect of the chloride template,
providing an appropriate folded conformation of the openchain
precursor and reducing the energy barrier for the
formation of the macrocyclic product. [-]
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The Journal of Organic Chemistry, Article ASAPDerechos de acceso
ACS AuthorChoice - This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
Copyright © 2016 American Chemical Society
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/openAccess
Copyright © 2016 American Chemical Society
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/openAccess
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