Mañana, JUEVES, 24 DE ABRIL, el sistema se apagará debido a tareas habituales de mantenimiento a partir de las 9 de la mañana. Lamentamos las molestias.
Stereochemical diversity in pyrrolidine synthesis by catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides
Entity
UAM. Departamento de Química OrgánicaPublisher
Royal Society of ChemistryDate
2019-10-14Citation
10.1039/C9CC05238K
Chemical Communications 55.80 (2019): 11979-11991
ISSN
1364-548X (online); 1359-7345 (print)DOI
10.1039/C9CC05238KFunded by
We acknowledge the Spanish Ministerio de Economía, Industria y Competitividad (Grant CTQ2015-66954-P, MINECO/FEDER, UE) and FEDER/Ministerio de Ciencia, Innovación y Universidades – Agencia Estatal de Investigación (Grant PGC2018-098660-B-I00) for financial supportProject
Gobierno de España. CTQ2015-66954-P; Gobierno de España. PGC2018-098660-B-I00Editor's Version
https://doi.org/10.1039/C9CC05238KSubjects
Pyrrolidines; QuímicaRights
© The Royal Society of Chemistry 2019Abstract
The pyrrolidine ring is a privileged structural motif in synthetic and medicinal chemisty. This review aims to highlight the high versatility of the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides for access to different types of stereochemical patterns in enantioselective pyrrolidine synthesis. Special attention will be paid to stereodivergent procedures giving rise to different stereoisomers from the same starting materials
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Google Scholar:Adrio Sevilla, Francisco Javier
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Carretero Gonzálvez, Juan Carlos
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