Isothiourea-Catalyzed Enantioselective α-Alkylation of Esters via 1,6-Conjugate Addition to <i>para</i>-Quinone Methides
The isothiourea-catalyzed enantioselective 1,6-conjugate addition of <i>para</i>-nitrophenyl esters to 2,6-disubstituted <i>para</i>-quinone methides is reported. <i>para</i>-Nitrophenoxide, generated in situ from initial <i>N</i>-acylation of the isot...
Guardado en:
Autores principales: | Jude N. Arokianathar, Will C. Hartley, Calum McLaughlin, Mark D. Greenhalgh, Darren Stead, Sean Ng, Alexandra M. Z. Slawin, Andrew D. Smith |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/355f0306f6ad4c5f949bcd0c0470370b |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Organocatalytic Asymmetric [2 + 4] Cycloadditions of 3-Vinylindoles with <i>ortho</i>-Quinone Methides
por: Si-Jia Liu, et al.
Publicado: (2021) -
Oxidative Transformations of 3,4-Dihydroxyphenylacetaldehyde Generate Potential Reactive Intermediates as Causative Agents for Its Neurotoxicity
por: Shosuke Ito, et al.
Publicado: (2021) -
EFFECT OF SOME NATURAL UV-ABSORBERS ON THE PHOTOSTABILIZATION OF ACTIVE INGREDIENTS IN GERMAN CHAMOMILLE FLORAL EXTRACTS: PART I
por: LUCERO,A, et al.
Publicado: (2012) -
EFFICIENT SYNTHESIS OF NOVEL TRICYCLIC BENZOXAZINE DERIVATIVE VIA RING OPENING OF EPOXIDE ALONG THE MP AND DFT STUDIES OF STRUCTURAL, SPECTROSCOPIC (IR, RAMAN, UV-VIS), THERMODYNAMIC, ORBITALS AND NLO PROPERTIES OF DESIRED TRICYCLIC BENZOXAZINE DERIVATIVE
por: Mansha,Asim, et al.
Publicado: (2020) -
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.)
por: BUONO-CORE,G. E, et al.
Publicado: (2011)