Study of the Stereoselectivity of the Nucleophilic Epoxidation of 3-Hydroxy-2- methylene Esters
Ver/ Abrir
Impacto
Scholar |
Otros documentos de la autoría: Latorre, Antonio; Sáez Cases, José Antonio; Rodríguez, Santiago; González, Florenci
Metadatos
Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7033
comunitat-uji-handle3:10234/8618
comunitat-uji-handle4:
INVESTIGACIONMetadatos
Título
Study of the Stereoselectivity of the Nucleophilic Epoxidation of 3-Hydroxy-2- methylene EstersFecha de publicación
2013-01Editor
ElsevierCita bibliográfica
LATORRE, Antonio, et al. Study of the stereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters. Tetrahedron, 2014, 70.1: 97-102.Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://www.sciencedirect.com/science/article/pii/S004040201301702XVersión
info:eu-repo/semantics/acceptedVersionPalabras clave / Materias
Resumen
The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita–Baylis–Hillman reaction. The resulting epoxy ... [+]
The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita–Baylis–Hillman reaction. The resulting epoxyesters were treated with thiophenol for transformation into 2,3-dihydroxy-2-((phenylthio)methyl), which upon treatment with triphosgene afforded the corresponding cyclic carbonates. [-]
Publicado en
Tetrahedron Volume 70, Issue 1, 7 January 2014Derechos de acceso
Copyright © 2014 Elsevier B.V.
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/openAccess
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/openAccess
Aparece en las colecciones
- QUI_Articles [299]