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1.
Bioorg Med Chem Lett ; 19(1): 199-202, 2009 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-19013793

RESUMEN

The P4 region of a series of oxamyl dipeptide caspase inhibitors was optimized by the combination of anti-apoptotic activity in the Jurkat/Fas (JFas) cellular assay and membrane permeability in the PAMPA assay. Two highly potent anti-apoptotic agents with moderate membrane permeability, 29 and 36, showed strong in vivo efficacy in a murine model of alpha-Fas-induced liver injury.


Asunto(s)
Inhibidores de Caspasas , Inhibidores de Cisteína Proteinasa/síntesis química , Hepatopatías/tratamiento farmacológico , Animales , Apoptosis/efectos de los fármacos , Permeabilidad de la Membrana Celular/efectos de los fármacos , Inhibidores de Cisteína Proteinasa/farmacología , Humanos , Células Jurkat , Ratones , Relación Estructura-Actividad , Receptor fas
2.
J Am Chem Soc ; 127(33): 11610-1, 2005 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-16104731

RESUMEN

Tertiary amides, ureas, and amines undergo direct intermolecular addition to aldehydes under the Et3B/air conditions, thereby providing a unique and simple means for the radical sp3 C-H transformation of nitrogen-containing molecules.


Asunto(s)
Amidas/síntesis química , Aminas/síntesis química , Nitrógeno/química , Ureasa/síntesis química , Alquilación , Amidas/química , Aminas/química , Radicales Libres/química , Estructura Molecular , Ureasa/química
3.
J Org Chem ; 70(6): 2342-5, 2005 Mar 18.
Artículo en Inglés | MEDLINE | ID: mdl-15760227

RESUMEN

[reaction: see text] Epsilonthers and an acetal were found to undergo direct intermolecular addition to aldehydes under the Et(3)B/air conditions. This study presents a very unique and simple means for the radical alpha-C-H hydroxyalkylation of oxygen-containing compounds.


Asunto(s)
Acetales/síntesis química , Éteres/síntesis química , Alquilación , Radicales Libres/química , Conformación Molecular
4.
J Org Chem ; 69(26): 9262-8, 2004 Dec 24.
Artículo en Inglés | MEDLINE | ID: mdl-15609965

RESUMEN

Alkoxyl radicals have a wide range of applications in organic synthesis due to their remarkable chemical properties in molecular transformation. The present study shows two types of alkoxyl radicals (primary vs tertiary) to selectively undergo dehydrogenation and beta-scission to give rise to key structural elements of (-)-CP-263,114 (1). By alkoxyl radical transformation followed by installation of the C19-C25 (CP numbering) side chain and the bridged bisacetal unit, the functionalized CP precursor 2 was obtained.


Asunto(s)
Anhídridos Maleicos/síntesis química , Espectroscopía de Resonancia Magnética , Anhídridos Maleicos/química
5.
J Org Chem ; 68(2): 625-7, 2003 Jan 24.
Artículo en Inglés | MEDLINE | ID: mdl-12530897

RESUMEN

The alpha-hydroxyalkylation of tetrahydrofuran with aldehydes via radical C-H abstraction was conducted using triethylborane in the presence of tert-butyl hydroperoxide. This study presents a rare instance of direct intermolecular radical addition of unactivated cyclic ether to aldehydes.

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