[][com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=86663]], camposKey:0022-3263 2024-01-05 Enantioselective Amination of 4-Substituted Pyrazolones Catalyzed by Oxindole-Containing Thioureas and by a Recyclable Linear-Polymer-Supported Analogue in a Continuous Flow Process330344, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=77616]], camposKey:0022-3263 2023-01-01 Access to Spiropyrazolone-butenolides through NHC-Catalyzed [3 + 2]-Asymmetric Annulation of 3-Bromoenals and 1H-Pyrazol-4,5-diones00, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=74118]], camposKey:1477-0539 2023-01-01 Organocatalytic asymmetric synthesis of oxazolidino spiropyrazolinones via N,O-acetalization/aza Michael addition domino reaction between N-Boc pyrazolinone ketimines and ¿-hydroxyenones00, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=65694]], camposKey:2052-4129 2022-01-18 NHC-catalysed [3+2]-asymmetric annulation between pyrazolin-4,5-diones and enals: synthesis of novel spirocyclic pyrazolone gamma-butyrolactones and computational study of mechanism and stereoselectivity420427, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=72318]], camposKey:1420-3049 2022-01-01 Squaramide-Catalyzed Asymmetric Mannich Reaction between 1,3-Dicarbonyl Compounds and Pyrazolinone Ketimines: A Pathway to Enantioenriched 4-Pyrazolyl- and 4-Isoxazolyl-4-aminopyrazolone Derivatives00, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=65613]], camposKey:1477-0520 2020-12-07 Bifunctional thiourea-modified polymers of intrinsic microporosity for enantioselective ¿-amination of 3-aryl-2-oxindoles in batch and flow conditions92759283, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=54741]], camposKey:1615-4150 2020-01-01 Supported Bifunctional Chiral Thioureas as Catalysts in the Synthesis of 3-Amino-2-Oxindoles through Enantioselective aza-Friedel-Crafts Reaction: Application in Continuous Flow Processes112, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=50494]], camposKey:1434-193X 2019-01-01 Chiral Bifunctional Thiosquaramides as Organocatalysts in the Synthesis of Enantioenriched 3,3-Disubstituted Oxindoles65396549, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=46744]], camposKey:2073-4360 2019-01-01 Chiral Bifunctional Thioureas and Squaramides Grafted into Old Polymers of Intrinsic Microporosity for Novel Applications130, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=46746]], camposKey:1615-4150 2019-01-01 Synthesis of Enantioenriched 3-Amino-3-Substituted Oxindoles by Stereoselective Mannich Reaction Catalyzed by Supported Bifunctional Thioureas36453655, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=39736]], camposKey:0022-3263 2018-01-01 Chiral Bifunctional Thioureas and Squaramides and Their Copolymers as Recoverable Organocatalysts. Stereoselective Synthesis of 2-Substituted 4-Amino-3-nitrobenzopyrans and 3-Functionalized 3,4-Diamino-4H-Chromenes55465557, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=46745]], camposKey:2470-1343 2018-01-01 Diastereo- and Enantioselective Syntheses of Trisubstituted Benzopyrans by Cascade Reactions Catalyzed by Monomeric and Polymeric Recoverable Bifunctional Thioureas and Squaramides1659116600, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=4414]], camposKey:1434-193X 2017-01-01 Biodegradable Chitosan-Derived Thioureas as Recoverable Supported Organocatalysts - Application to the Stereoselective Aza-Henry Reaction36583665, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=42875]], camposKey:1861-194X 2017-01-01 Chiral Fullerene-Derived Thioureas as Recyclable Asymmetric Organocatalysts8660, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=4415]], camposKey:1434-193X 2017-01-01 Recyclable Chiral Bifunctional Thioureas Derived from [60]Fullerene and Their Use as Highly Efficient Organocatalysts for the Asymmetric Nitro-Michael Reaction26832691, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=4413]], camposKey:0022-3263 2017-01-01 Supported and Unsupported Chiral Squaramides as Organocatalysts for Stereoselective Michael Additions: Synthesis of Enantiopure Chromenes and Spirochromanes84448454, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2455]], camposKey:2192-6506 2016-01-01 Bottom-Up Synthesis of Supported Thioureas and Their Use in Enantioselective Solvent-Free Aza-Henry and Michael Additions8692, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=9798]], camposKey:2046-2069 2016-01-01 Enantioselective synthesis of seven-membered carbo- and heterocyles by organocatalyzed intramolecular Michael addition3016630169, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=50507]], camposKey:2365-6549 2016-01-01 Short Synthesis of Novel Recyclable Chiral Bifunctional Thioureas from Aminoalkyl Polystyrene and their use as Organocatalysts in Stereoselective aza¿Henry Reaction50575061, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=4416]], camposKey:1860-5397 2016-01-01 Supported bifunctional thioureas as recoverable and reusable catalysts for enantioselective nitro-Michael reactions628635, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2427]], camposKey:1463-9262 2015-01-01 Chiral ureas and thioureas supported on polystyrene for enantioselective aza-Henry reactions under solvent-free conditions22172225, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2409]], camposKey:2046-2069 2015-01-01 The organocatalyzed domino Michael-aldol reaction revisited. Synthesis of enantioenriched 3-hydroxycyclohexanone derivatives by reaction of enals with alpha,alpha '-diaryl-substituted acetone6597565981, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2428]], camposKey:0022-3263 2014-01-01 One-Pot Sequential Organocatalytic Michael-Tishchenko-Lactonization Reactions. Synthesis of Enantioenriched 4,5,6-Trisubstituted delta-Lactones86388644, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2451]], camposKey:1434-193X 2014-01-01 Organocatalytic Domino Michael-Heterocyclization Reaction of alpha,beta-Unsaturated Aldehydes and alpha-Cyano Ketones: Synthesis of Enantioenriched 4,5,6-Trisubstituted 3,4-Dihydropyranones80728076, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2452]], camposKey:0040-4039 2013-06-12 Novel supported and unsupported prolinamides as organocatalysts for enantioselective cyclization of triketones31013104, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2447]], camposKey:0040-4020 2013-01-01 Novel sulfonylpolystyrene-supported prolinamides as catalysts for enantioselective aldol reaction in water1081110819, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2464]], camposKey:0936-5214 2011-09-01 Direct Experimental Evidence for the Epimerization of Diastereoisomers in the Enantioselective Organocatalyzed Michael Addition of Acetoacetates to Nitroolefins22032205, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2492]], camposKey:0947-6539 2011-01-01 Enantioselective Conjugate Addition of Nitro Compounds to alpha,beta-Unsaturated Ketones: An Experimental and Computational Study59315938, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2440]], camposKey:1477-0520 2011-01-01 Highly diastereo- and enantioselective direct Barbas-List aldol reactions promoted by novel benzamidoethyl and benzamidopropyl prolinamides in water935940, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2441]], camposKey:1615-4150 2010-12-17 Stereocontrolled Construction of Quaternary Stereocenters by Inter- and Intramolecular Nitro-Michael Additions Catalyzed by Bifunctional Thioureas33643372, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2435]], camposKey:1434-193X 2010-09-01 L-Prolinamides Derived from Chiral and Achiral 1,2-Diamines as Useful Bifunctional Organocatalysts for Direct Diastereo- and Enantioselective Aldol Reaction53105319, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2414]], camposKey:0022-3263 2010-08-06 Synthesis of both Enantiomers of Hemiesters by Enantioselective Methanolysis of Meso Cyclic Anhydrides Catalyzed by alpha-Amino Acid-Derived Chiral Thioureas54175420, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2415]], camposKey:0947-6539 2008-01-01 Novel bifunctional chiral urea and thiourea derivatives as organocatalysts: Enantioselective nitro-Michael reaction of malonates and diketones51165119, 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=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=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=2418]], camposKey:0040-4020 2000-03-10 A practical stereoselective synthesis of both enantiomers of threo- and erythro-beta-hydroxy norvaline from (S)-serine derivatives15231531, 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=2416]], camposKey:0957-4166 1998-07-17 A facile stereodivergent synthesis of threo- and erythro-N,N-dibenzyl sphingosines from (S)-N,N-dibenzyl-O-TBDMS-serinal24932498, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2436]], camposKey:0040-4020 1998-05-21 Stereodivergent synthesis of all diastereomers of 4-aminoheptane-3,5-diol from (L)-serine56075616, 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=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=53227]], camposKey:0039-7881 1994-01-01 Synthesis of [1]Benzopyrano[4,3-b]pyrrol-4(1H)-ones from 4-Chlorocoumarin279281, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=6152]], camposKey:0040-4039 1993-01-01 Improved stereoselective methods of triene and diene synthesis: A novel application of Na(Hg).28352838, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2446]], camposKey:0039-7881 1991-05-01 AN IMPROVED SYNTHESIS OF 2H-1,2,6-THIADIAZINE 1,1-DIOXIDES BY CONDENSATION OF BETA-AMINO AND BETA-CHLORO ALPHA,BETA-UNSATURATED KETONES WITH SULFAMIDES355356, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=57349]], camposKey:0039-7881 1991-01-01 An improved synthesis of 2H-1,2,6-thiadiazine 1,1-dioxides by condensation of ß-amino and ß-chloro ¿,ß-unsaturated ketones with sulfamides355356, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2445]], camposKey:0385-5414 1990-06-01 THE REACTION OF BETA-AMINOENONES WITH ALPHA-AMINO DERIVATIVES - SYNTHESIS OF 2-FUNCTIONALIZED PYRROLES10491058, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2431]], camposKey:0300-922X 1990-01-01 DIFFERENTIAL REACTIVITY OF BETA-AMINO ENONES AND 3-DIMETHYLAMINOACRYLALDEHYDE TOWARDS ALPHA-AMINO DERIVATIVES26812685, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2480]], camposKey:0039-7911 1990-01-01 REGIOSELECTIVE SYNTHESIS OF 2-FUNCTIONALIZED THIOPHENES BY CONDENSATION OF ALPHA-MERCAPTO COMPOUNDS WITH BETA-AMINOENONE DERIVATIVES25372547, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2460]], camposKey:0385-5414 1989-10-01 REGIOSELECTIVE SYNTHESIS OF 2-ACYLPYRROLES AND 3-ACYLPYRROLES BY REACTION OF BETA-AMINOENONES WITH ALPHA-AMINOKETONE HYDROCHLORIDE19831991, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=2443]], camposKey:0385-5414 1989-10-01 SOME OBSERVATIONS ON THE REACTIVITY OF BETA-AMINOENONES TOWARDS PHENACYLAMINE HYDROCHLORIDE19731982][CapitolsLlib{id=com.sigma.fs3.argos.domain.gpc.GpcCapitolsLlibPK[ifcactivitat=CAP, ifccomptador=19251]},camposKey: 120 139 Prolinamides as Asymmetric Organocatalysts 978-1-78262-209-3Sustainable Catalysis: Without Metals or Other Endangered Elements Pt 1 1 2015-01-01 Royal Society of Chemistry][][Llibres{id=com.sigma.fs3.argos.domain.gpc.GpcLlibresPK[ifcactivitat=LLI, 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