Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

1,2-Stereochemical induction in the Pd(II)-Catalyzed conjugate addition of boronic acids

dc.contributor.authorRoscales García, Silvia
dc.contributor.authorSánchez, Francisco
dc.contributor.authorGarcía Csaky, Aurelio
dc.date.accessioned2025-01-21T11:05:10Z
dc.date.available2025-01-21T11:05:10Z
dc.date.issued2015
dc.description.abstractPd(II) catalysis has been used for substrate-controlled 1,2-stereoselective conjugate addition of boronic acids to enantiopure α,β-acyclic unsaturated ketones and esters without competition from the Mirozoki–Heck reaction. Best results were found with Bedford's palladacycle. The reaction with cyclic derivatives of Garner's aldehyde also took place with high levels of trans diastereoselectivity.
dc.description.departmentDepto. de Química Orgánica
dc.description.facultyInstituto Pluridisciplinar (IP)
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationEur. J. Org. Chem. 2015, 1754–1763
dc.identifier.doi10.1002/ejoc.201403488
dc.identifier.officialurlhttps://doi.org/10.1002/ejoc.201403488
dc.identifier.urihttps://hdl.handle.net/20.500.14352/115321
dc.journal.titleEuropean Journal of Organic Chemistry
dc.language.isoeng
dc.page.final1763
dc.page.initial1754
dc.rights.accessRightsrestricted access
dc.subject.cdu547
dc.subject.ucmQuímica orgánica (Química)
dc.subject.unesco2306 Química Orgánica
dc.title1,2-Stereochemical induction in the Pd(II)-Catalyzed conjugate addition of boronic acids
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublicationef4f93d7-a007-4514-9055-f8ba8c41138d
relation.isAuthorOfPublication20fb9911-4424-43a0-ad98-890ff7a6dacd
relation.isAuthorOfPublication.latestForDiscoveryef4f93d7-a007-4514-9055-f8ba8c41138d

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
9. Eur. J. Org. Chem. 2015, 1754-1763.pdf
Size:
864.5 KB
Format:
Adobe Portable Document Format

Collections