The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
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Trypanosoma cruzi cell death induced by the Morita-Baylis-Hillman adduct 3-Hydroxy-2-methylene-3-(4-nitrophenylpropanenitrile)Multivalency as a key factor for high activity of selective supported organocatalysts for the Baylis-Hillman reaction.Regioselective SN2' Mitsunobu reaction of Morita-Baylis-Hillman alcohols: A facile and stereoselective synthesis of α-alkylidene-β-hydrazino acid derivatives.Enantioselective Nazarov Cyclization Catalyzed by a Cinchona Alkaloid Derivative.Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs.Recent developments of ketene dithioacetal chemistry.Catalytic asymmetric synthesis of allylic alcohols and derivatives and their applications in organic synthesis.Recent advances in organocatalytic methods for asymmetric C-C bond formation.Cooperative Trifunctional Organocatalysts for Proficient Proton Transfer Reactions.Morita-Baylis-Hillman (MBH) Reaction Derived Nitroallylic Alcohols, Acetates and Amines as Synthons in Organocatalysis and Heterocycle Synthesis.Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita-Baylis-Hillman alcohols.Antimicrobial activity of allylic thiocyanates derived from the Morita-Baylis-Hillman reaction.Photoswitchable interlocked thiodiglycolamide as a cocatalyst of a chalcogeno-Baylis-Hillman reaction.Crystal structure of 3-(3,4,5-tri-meth-oxy-phen-yl)-1,2,3,4-tetra-hydro-cyclo-penta[b]indole-2-carb-oxy-lic acid.Reactions of nitroxides XIII: Synthesis of the Morita-Baylis-Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, and DABCO and quinuclidine as catalysts.An example of enzymatic promiscuity: the Baylis-Hillman reaction catalyzed by a biotin esterase (BioH) from Escherichia coli.Direct β-acylation of 2-arylidene-1,3-indandiones with acyl chlorides catalyzed by organophosphanes.Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.Baylis-Hillman bromides as a source of 1,3-dipoles: sterically directed synthesis of oxindole-fused spirooxirane and spirodihydrofuran frameworks.Gold(I)-Assisted α-Allylation of Enals and Enones with Alcohols.Catalytic MBH reaction of β-substituted nitroalkenes with azodicarboxylates.Morita-Baylis-Hillman Reaction of β,β-Disubstituted Enones: An Enantioselective Organocatalytic Approach for the Synthesis of Cyclopenta[b]annulated Arenes and Heteroarenes.A computational investigation of the solvent-dependent enantioselective intramolecular Morita-Baylis-Hillman reaction of enones.Hexafluoroisopropanol mediated benign synthesis of 2H-pyrido[1,2-a]pyrimidin-2-ones by using a domino protocol.Mechanism and reactivity in the Morita-Baylis-Hillman reaction: the challenge of accurate computations.Highly regio- and diastereo-selective synthesis of novel tri- and tetra-cyclic perhydroquinoline architectures via an intramolecular [3 + 2] cycloaddition reaction.Asymmetric aza-Morita-Baylis-Hillman reactions of chiral N-phosphonyl imines with acrylates via GAP chemistry/technology.Synthesis of 4H-chromenes by an unexpected, K3PO4-mediated intramolecular Rauhut-Currier type reaction.An enantioselective organocatalyzed aza-Morita-Baylis-Hillman reaction of isatin-derived ketimines with acrolein.A multicomponent cascade reaction for the synthesis of novel chromenopyranpyrazole scaffolds.Synthesis and Evaluation of Baylis-Hillman Reaction Derived Imidazole and Triazole Cinnamates as Antifungal Agents
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Q28542102-629320F2-1CD9-42E1-92C3-8046C87ABB48Q30868138-3708BECF-1B54-44F0-99C2-63C9623F60C3Q33830058-4B55AA9D-97BD-4B43-B02F-AC1D78A98283Q35733806-5D695BBF-1F5F-4BFA-9B6B-DC4F535BF436Q37495686-32520396-050B-4AA0-8F55-EC23FBABA5E6Q38059359-0D71728F-5E0F-4F24-ACB5-4188717E6D05Q38074104-CDF2432B-6F74-45D9-B011-EAA24067BD16Q38151648-AA65D30B-0607-41BD-8DF9-8E0BF529963BQ38806641-51828DB8-46B1-41C0-8F1B-E7E19E1459CFQ38972019-9B08EC78-7795-4275-8F7A-495B129B5B0CQ41812976-49E47205-D9F6-45F7-B96F-DF5D1C73F11BQ41919747-FB73E522-D6CC-4362-A2C0-3CFA0CF01586Q42257922-8BE970FD-888A-43D0-BB02-CA7FA622F937Q42589032-67423785-E565-4A9B-B883-4C76F239D963Q42608528-16FAC888-8FA4-43BE-8294-84ACFE0A0DF2Q45344007-BBABBF94-2907-4388-ABD0-79EEAA75C922Q45938475-B8C22286-2CF4-4583-ADBF-7235F167AD71Q46452753-44B6FA54-9A21-4EDD-9CE7-0F4C023F5511Q46544940-D13D8D3C-9325-47D3-9F98-439268DDB810Q46653167-A1D31974-7FC5-45B0-A2E6-4049EFABCCA7Q46888100-7F124F7A-851C-4EF7-8749-E0346609C62DQ48275940-BD058E2B-E86E-410C-8B70-D1E14261B923Q49611556-CE47F582-84FD-432F-9B15-AF11C16D9405Q50073712-A3F91440-21FF-4BA3-B062-B5F2AEAB0A72Q50109323-396BE6AE-7CCD-4BEB-A1EB-C8F41BE79818Q51014837-B2003FF1-A960-4473-A3AD-1DEA4A15FEE2Q51315056-BAE68BF5-35A1-44E7-928B-8E2B757D9C29Q53686520-102FC68F-B0E8-43ED-A554-49DC88BD5323Q54264206-30A4AEBC-05EC-493D-969F-6C97A64F17A8Q54753353-455A1060-2FA1-490F-9E6B-156791A0866AQ58555610-B29BBFD1-5C35-4A68-A255-84D6A6E98D3E
P2860
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
@en
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
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type
label
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
@en
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
@nl
prefLabel
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
@en
The Baylis-Hillman reaction: a novel concept for creativity in chemistry.
@nl
P2860
P356
P1476
The Baylis-Hillman reaction: a novel concept for creativity in chemistry
@en
P2093
Deevi Basavaiah
P2860
P356
10.1039/C1CS15174F
P577
2011-09-06T00:00:00Z