Inicio > PEREZ ENCABO, ALFONSO

PEREZ ENCABO, ALFONSO

PROFESORES TITULARES DE UNIVERSIDAD
Química Orgánica
SÍNTESIS ASIMÉTRICA
 
alfonso.perez.encabo@uva.es
0

Índice H en Web of Science: 16
Índice H en Scopus: 17
 
Enlazar esta página

[][com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=46747]], camposKey:0020-1669 2018-01-01 Copper Complexes in the Promotion of Aldol Addition to Pyridine-2-carboxaldehyde: Synthesis of Homo- and Heteroleptic Complexes and Stereoselective Double Aldol Addition264276, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8745]], camposKey:1477-0520 2015-01-01 7-endo selenocyclization reactions on chiral 3-prenyl and 3-cinnamyl-2-hydroxymethylperhydro-1,3-benzoxazine derivatives. A way to enantiopure 1,4-oxazepanes91189126, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2430]], camposKey:0040-4020 2012-11-11 (-)-8-Amino menthol-derived perhydrobenzoxazines as chiral templates and masked aldehydes in the diastereoselective intermolecular Pauson-Khand reaction92939300, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2425]], camposKey:1434-193X 2012-02-01 Studies on the Diastereoselective Intramolecular Pauson-Khand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (-)-8-Aminomenthol12021208, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2473]], camposKey:1434-193X 2007-04-01 Synthesis of enantioenriched 2- and 2,6-substituted piperidin-3-ols from alpha-dibenzylamino aldehydes18031810, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2486]], camposKey:0040-4020 2006-08-14 Diastereoselective synthesis of enantioenriched homopropargyl amino alcohols from alpha-dibenzylamino aldehydes and their use as chiral synthons77837792, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2497]], camposKey:1434-193X 2006-07-24 Diastereoselective ethynylation of chiral alpha-(dibenzylamino) aldehydes: Synthesis of meso- and homochiral C-2-symmetrical 1,6-diamino-2,5-diols34423450, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2489]], camposKey:0040-4039 2006-07-24 Diastereoselective syntheses of 2-amino propargyl alcohols. Chiral building blocks for enantiopure amino gamma-lactones and 5-hydroxy-piperidinone derivatives53175320, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2475]], camposKey:0936-5214 2004-09-06 Diastereoselective cyclization of gamma-delta epoxyketones with (-)-phenylglycinol: Synthesis of both enantiomers of cis-5-alkyl-2-hydroxymethyl pyrrolidines20162018, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2429]], camposKey:0936-5214 2004-06-03 Base-dependent regio- and diastereoselective alkylation of chiral perhydro 1,3,2-oxazabenzophosphorinane-2-oxides derived from (-)-8-benzylamino menthol13001302, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2491]], camposKey:1434-193X 2004-03-26 Diastereoselective synthesis of beta-amino-alpha-(trifluoromethyl) alcohols from homochiral alpha-dibenzylamino aldehydes15581566, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2490]], camposKey:1434-193X 2003-08-25 Manipulating L-aspartic and L-glutamic acids - Diastereoselective synthesis of enantiopure beta-amino-gamma-hydroxy acids and gamma-amino-delta-hydroxy acids33873397, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2488]], camposKey:0040-4020 2001-10-01 Diastereoselective synthesis of enantiopure gamma-amino-beta-hydroxy acids by Reformatsky reaction of chiral alpha-dibenzylamino aldehydes85218530, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2487]], camposKey:0957-4166 2001-06-22 Stereoselective synthesis of (5S,6S)- and (5S,6R)-aza-muricatacin from an L-glutamic acid derivative15031509, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2504]], camposKey:0002-7863 2001-03-07 Diastereoselective tandem 6-exo carbolithiation intramolecular ring opening in (-)-8-aminomenthol-derived perhydrobenzoxazines. A new synthesis of enantiopure 4-substituted tetrahydro isoquinolines and 2-azabenzonorbornanes18171821, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2477]], camposKey:0957-4166 2001-02-19 Stereoselective cyanation of chiral alpha-amino aldehydes by reaction with Nagata's reagent: a route to enantiopure beta-amino-alpha-hydroxy acids347353, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=47585]], camposKey:0039-7881 2001-01-01 Synthesis of [1]Benzopyrano[4,3-b]pyrrol-4(1H)-ones from 4-chloro-3-formylcoumarin19411948, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=3746]], camposKey:0008-4042 2001-01-01 Tautomerization tendencies of 2-acetylcycloalkanones, 2-acetyl-1,3-cycloalkanediones, and cyclic ß-keto esters of five- and six-membered rings448454, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2483]], camposKey:0040-4020 2000-02-25 Synthesis of chiral, non-racemic aldols from chiral beta-hydroxy-Weinreb amides prepared by enantioselective Reformatsky-like reaction induced by chiral beta-aminoalcohols12171223, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2496]], camposKey:1434-193X 2000-01-01 A simple stereoselective synthesis of enantiopure 2-substituted pyrrolidines and piperidines from chiral (R)-phenylglycinol-derived bicyclic 1,3-oxazolidines17191726, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=6173]], camposKey:0040-4020 2000-01-01 Synthesis of chiral non-racemic aldols from chiral beta-hydroxy-Weinreb amides prepared by enantioselective Reformatsky-like reaction induced by chiral beta-aminoalcohols12171223, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2501]], camposKey:0040-4020 1999-12-03 Efficient synthesis of syn-aziridino alcohols by chelation-controlled addition of dialkylzincs and Grignard reagents to N-benzylaziridino aldehydes1413714144, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2421]], camposKey:0040-4020 1997-03-10 Enantioselective reformatsky reaction induced by chiral beta-amino alcohols37873794, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2439]], camposKey:0022-3263 1996-06-28 Synthesis of enantiopure syn-beta-amino alcohols. A simple case of chelation-controlled additions of diethylzinc to alpha-(dibenzylamino) aldehydes42104213, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=39737]], camposKey:0039-7881 1996-01-01 Synthesis of chiral alpha,alpha-difluoro-beta-hydroxy esters by enantioselective Reformatsky reaction10701072, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=47587]], camposKey:1472-7781 1994-12-01 Oxidation of alkylthio substituted tricarbonyl(¿6-arene)chromium(0) complexes to alkylsulfinyl substituted tricarbonyl(¿6-arene) chromium(0) complexes629642, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2472]], camposKey:0957-4166 1994-01-01 EASY PREPARATION OF ENANTIOPURE C-2-SYMMETRICAL AMINOALCOHOLS DERIVED FROM M-XYLYLENE DIAMINE5766, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2405]], camposKey:0957-4166 1994-01-01 ENANTIOSELECTIVE ETHYLATION OF ALDEHYDES CATALYZED BY CHIRAL C-2-SYMMETRICAL BETA-HYDROXY-M-XYLYLENE DIAMINES6772, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=47588]], camposKey:0022-4936 1993-12-01 First synthesis of sulfinyl substituted tricarbonyl(¿6- arene)chromium(0) complexes10591062, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2495]], camposKey:0040-4039 1992-08-11 A NEW CHIRAL GLYCINE SYNTHON - SYNTHESIS, X-RAY STRUCTURE OF (-)BULLET(2S,4R)-2-ETHOXYCARBONYL-4-PHENYL-1,3-OXAZOLIDINE AND DIASTEREOSELECTIVE NUCLEOPHILIC RING-OPENING TO (R)-ETHYL ALPHA-AMINO CARBOXYLATES47434746, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2406]], camposKey:0040-4039 1992-05-12 STEREOSELECTIVE RING-OPENING OF CHIRAL OXAZOLIDINES BY REFORMATSKY REAGENTS - AN ENANTIOSELECTIVE ENTRY TO BETA-AMINO ESTERS28952898, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=46786]], camposKey:0936-5214 1992-01-01 Regio- and stereocontrolled nucleophilic ring opening of chiral oxazolidines by diethylaluminum cyanidea short and efficient route to enantiomerically enriched ¿-Amino Esters4547][][][][][][][][][][][com.sigma.fs3.argos.domain.gpc.GpcTesis[id=com.sigma.fs3.argos.domain.gpc.GpcTesisPK[ifcactivitat=TES, ifccomptador=70029]]][][][][][][][][][][com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c1, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4bf, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4bd, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c3, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c2, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4cd, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c7, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4d3, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4d1, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4d2, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4be, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4d0, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c8, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c5, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4cc, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c4, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c0, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4cf, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4ce, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4cb, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4ca, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c9, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@36b4c6, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@372d98, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@372c42, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@372dab, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@372b16, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@372255, com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ConvenisPPC@3725fe][][][][][][][][com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@414e46], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@4130eb], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@41255a], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@413bdd], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@46089a], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@411dbe], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@460772], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@460753], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@4605cb], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@411e46], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@460451], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@4133fa], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@41221a], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@45f3fc], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@45f43a], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@413841], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@413b22], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@45f34d], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@413b42]][][][com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@14f79, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@14cdc, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13734, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13b41, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13af6, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@143cb, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13fb0][]

AYUDA A LA INVESTIGACIÓN

PUBLICACIONES

Artículos de revista (32)

Alvarez-Miguel, L.; Barbero, H.; Sacristan-Martin, A.; Martin Alvarez, J.M.; Perez-Encabo, A.; Alvarez, C.M.; Garcia-Rodriguez, R.; Miguel, D. Copper Complexes in the Promotion of Aldol Addition to Pyridine-2-carboxaldehyde: Synthesis of Homo- and Heteroleptic Complexes and Stereoselective Double Aldol Addition. Inorganic Chemistry 2018; 57(1): 264-276.
Enlace a la publicaciónTexto completo en acceso abierto
Ver Todos
 

AYUDA A LA INVESTIGACIÓN

Proyectos (19)

NUEVAS TIOUREAS Y ESCUARAMIDAS SOPORTADAS PARA REACCIONES ENANTIOSELECTIVAS EN PROCESOS DE FLUJO CONTINUO. PEDROSA SAEZ, RAFAEL (IP); ANDRES JUAN, CELIA (IP); PEREZ ENCABO, ALFONSO; NIETO ROMAN, FRANCISCO JAVIER; MAESTRO FERNANDEZ, ALICIA; ANDRES GARCIA, JOSE MARIA; INFANTE BLANCO, REBECA; ANDRES JUAN, CELIA. VA149G18. UNIVERSIDAD DE VALLADOLID (UVa), JUNTA DE CASTILLA Y LEÓN -CONSEJERÍA DE EDUCACIÓN 2018-2020
Ver Todos

Convenios (29)

CALTDYNAMICS_ FERNANDO VILLAFAÑEZ. PEREZ ENCABO, ALFONSO (IP); TURIEL HERNANDEZ, JOSE ANGEL. 2021
Ver Todos
 
Cargando información ...
Universidad de Valladolid - Copyright Universidad de Valladolid - Todos los derechos reservados