A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides

Autores
Rustoy, E. M.; Baldessari, A.; Monsalve, L. N.
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The absolute stereochemistry of novel chiral N-(2-hydroxylalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters. The method was validated for this particular case by computational experiments.
Fil: Rustoy, E. M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); Argentina
Fil: Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); Argentina
Fil: Monsalve, L. N. Instituto Nacional de Tecnología Industrial (INTI); Argentina
Fuente
Advances in Chemistry
Materia
Ésteres
Acrilatos
Estereoquímica
Lipasas
Modelos
Computación
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/3.0/
Repositorio
Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)
Institución
Instituto Nacional de Tecnología Industrial
OAI Identificador
nuevadc:Monsalve2014Conformational_pdf
Acceder
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oai_identifier_str nuevadc:Monsalve2014Conformational_pdf
network_acronym_str RIINTI
repository_id_str
network_name_str Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)
spelling A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamidesRustoy, E. M.Baldessari, A.Monsalve, L. N.ÉsteresAcrilatosEstereoquímicaLipasasModelosComputaciónThe absolute stereochemistry of novel chiral N-(2-hydroxylalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters. The method was validated for this particular case by computational experiments.Fil: Rustoy, E. M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); ArgentinaFil: Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); ArgentinaFil: Monsalve, L. N. Instituto Nacional de Tecnología Industrial (INTI); ArgentinaHindawi2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfMonsalve2014Conformational.pdfhttps://app.inti.gob.ar/greenstone3/sites/localsite/collect/nuevadc/index/assoc/Monsalve.dir/doc.pdfAdvances in Chemistryreponame:Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)instname:Instituto Nacional de Tecnología Industrialenginfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/3.0/openAccess2025-09-29T15:02:07Znuevadc:Monsalve2014Conformational_pdfinstacron:INTIInstitucionalhttps://app.inti.gob.ar/greenstone3/biblioOrganismo científico-tecnológicohttps://argentina.gob.ar/intihttps://app.inti.gob.ar/greenstone3/oaiserver?verb=Identifypfalcato@inti.gob.arArgentinaopendoar:2025-09-29 15:02:08.399Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI) - Instituto Nacional de Tecnología Industrialfalse
dc.title.none.fl_str_mv A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
title A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
spellingShingle A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
Rustoy, E. M.
Ésteres
Acrilatos
Estereoquímica
Lipasas
Modelos
Computación
title_short A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
title_full A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
title_fullStr A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
title_full_unstemmed A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
title_sort A conformational model for MTPA esters of chiral N-(2-Hydroxyalkyl)acrylamides
dc.creator.none.fl_str_mv Rustoy, E. M.
Baldessari, A.
Monsalve, L. N.
author Rustoy, E. M.
author_facet Rustoy, E. M.
Baldessari, A.
Monsalve, L. N.
author_role author
author2 Baldessari, A.
Monsalve, L. N.
author2_role author
author
dc.subject.none.fl_str_mv Ésteres
Acrilatos
Estereoquímica
Lipasas
Modelos
Computación
topic Ésteres
Acrilatos
Estereoquímica
Lipasas
Modelos
Computación
dc.description.none.fl_txt_mv The absolute stereochemistry of novel chiral N-(2-hydroxylalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters. The method was validated for this particular case by computational experiments.
Fil: Rustoy, E. M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); Argentina
Fil: Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales (FCEyN-UBA); Argentina
Fil: Monsalve, L. N. Instituto Nacional de Tecnología Industrial (INTI); Argentina
description The absolute stereochemistry of novel chiral N-(2-hydroxylalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters. The method was validated for this particular case by computational experiments.
publishDate 2014
dc.date.none.fl_str_mv 2014
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv Monsalve2014Conformational.pdf
https://app.inti.gob.ar/greenstone3/sites/localsite/collect/nuevadc/index/assoc/Monsalve.dir/doc.pdf
identifier_str_mv Monsalve2014Conformational.pdf
url https://app.inti.gob.ar/greenstone3/sites/localsite/collect/nuevadc/index/assoc/Monsalve.dir/doc.pdf
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/3.0/
openAccess
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/3.0/
openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hindawi
publisher.none.fl_str_mv Hindawi
dc.source.none.fl_str_mv Advances in Chemistry
reponame:Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)
instname:Instituto Nacional de Tecnología Industrial
reponame_str Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)
collection Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI)
instname_str Instituto Nacional de Tecnología Industrial
repository.name.fl_str_mv Repositorio Institucional del Instituto Nacional de Tecnología Industrial (INTI) - Instituto Nacional de Tecnología Industrial
repository.mail.fl_str_mv pfalcato@inti.gob.ar
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score 12.559606

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