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Unlocking the potential of supported liquid phase catalysts with supercritical fluids: low temperature continuous flow catalysis with integrated product separationMetal-Catalyzed Carboxylation of Organic (Pseudo)halides with CO2Tailor-made biocatalysts: combining thermodynamics, organic synthesis, molecular biology, biochemistry and microbiology for the design of enzyme selections.The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis.Catalyst recognition of cis-1,2-diols enables site-selective functionalization of complex moleculesX-ray crystal structure of teicoplanin A₂-2 bound to a catalytic peptide sequence via the carrier protein strategy.Function-Oriented Investigations of a Peptide-Based Catalyst that Mediates Enantioselective Allylic Alcohol Epoxidation.Directed Evolution of RebH for Catalyst-Controlled Halogenation of Indole C-H BondsStructure diversification of vancomycin through peptide-catalyzed, site-selective lipidation: a catalysis-based approach to combat glycopeptide-resistant pathogens.Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive CouplingsEnantioselective Synthesis of Spirooxindole Enols: Regioselective and Asymmetric [3+2] Cyclization of 3-Isothiocyanato Oxindoles with Dibenzylidene Ketones.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.Synthesis of 5'-O-DMT-2'-O-TBS Mononucleosides Using an Organic Catalyst.Orthogonality in organic, polymer, and supramolecular chemistry: from Merrifield to click chemistry.Catalytic asymmetric synthesis of enantioenriched heterocycles bearing a C-CF3 stereogenic center.Cycloaddition reactions of enoldiazo compounds.A general method for artificial metalloenzyme formation through strain-promoted azide-alkyne cycloaddition.Switchable divergent asymmetric synthesis via organocatalysis.Applications of Nonenzymatic Catalysts to the Alteration of Natural Products.Divergent C-H Insertion-Cyclization Cascades of N-Allyl Ynamides.Catalyst-Driven Scaffold Diversity: Selective Synthesis of Spirocycles, Carbazoles and Quinolines from Indolyl Ynones.Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions.Suzuki-Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C-N and C-O bonds.Highly chemoselective ruthenium(ii)-catalyzed direct arylation of cyclic and N,N-dialkyl benzamides with aryl silanes.Exo-selective reductive macrocyclization of ynals.Practical silyl protection of ribonucleosides.Reactivity change of cyclobutanols towards isocyanates: rhodium favors C-carbamoylation over O-carbamoylation.Site-selective reactions: Exploiting intramolecularity.Cobalt-catalyzed intramolecular olefin hydroarylation leading to dihydropyrroloindoles and tetrahydropyridoindoles.Aldehyde-selective Wacker-type oxidation of unbiased alkenes enabled by a nitrite co-catalyst.Divergent C-H Annulation for Multifused N-Heterocycles: Regio- and Stereospecific Cyclizations of N-Alkynylindoles.Palladium- and ruthenium-catalyzed cycloisomerization of enynamides and enynhydrazides: a rapid approach to diverse azacyclic frameworks.From Palladium to Brønsted Acid Catalysis: Highly Enantioselective Regiodivergent Addition of Alkoxyallenes to Pyrazolones.Selective Synthesis of Six Products from a Single Indolyl α-Diazocarbonyl Precursor.Iron-Catalyzed C-O Bond Activation: Opportunity for Sustainable Catalysis.Switching of Reaction Pathway from C-C Rollover to C-N Ring-Extension Annulation.μ-Oxo-Dinuclear-Iron(III)-Catalyzed O-Selective Acylation of Aliphatic and Aromatic Amino Alcohols and Transesterification of Tertiary Alcohols.Ligand- and Solvent-Controlled Regio- and Chemodivergent Carbonylative Reactions.The scope and mechanism of palladium-catalysed Markovnikov alkoxycarbonylation of alkenes.Palladium-Catalyzed Regioselective Synthesis of 3-Arylindoles from N-Ts-Anilines and Styrenes.
P2860
Q27003107-15EDD97B-289B-4ECD-9F0B-F38EBDCA3019Q28073303-79D9023D-9D51-4E10-AF82-3E4C220A00E8Q30392013-19F7E52B-DCB0-4EFA-9B4D-29E53F705B4CQ33797639-46DA900A-04FF-4F27-BB5F-BE33C767065AQ33942260-63598CC0-A287-4DC4-B7E1-9F2A3153EE1CQ34211592-5196C6F6-B905-4F38-AECB-C410DA48A902Q34472447-700AAF82-2D18-4E2D-A551-7538685E1A4FQ34532086-5C4833A1-6B79-4AAD-8B04-F3A438A0D0D3Q35190498-3AC94C6B-65A0-46BD-A6FE-F04BCF24737FQ35752222-B6C7620B-6CEB-4C79-AC7F-679945FEBA7DQ37167552-DA25B6A5-7C15-4339-AF63-0842819B5822Q38206709-990CA056-449D-41F7-818F-695A35A10C94Q38222909-54718246-F6AA-4B51-AFEF-E4D5FDD5CFC9Q38318861-A90679D2-CB01-4FEF-ACF9-F880A45FB747Q38367314-D296825D-D0BB-4036-A4D7-1DBEDC1C7753Q38654525-7E733FE8-B3F3-4C37-BBC4-C2CE0FE3EBBAQ38919572-389F0B75-90AC-406C-82CA-07B8464FD3B6Q39145237-80916102-32E7-4AF6-B321-B4BC9A5A064AQ39350547-F05B509E-BA80-42FE-825E-9EB336A2EB41Q40213790-56ECC312-2BE6-4C87-A064-DE2C9578A8E2Q41607485-48B258DA-C0C3-42A9-9554-EE29A5439D26Q41787281-A2CF3CF3-B68B-4417-B925-5153D06B80D3Q42278892-4A787FC6-56F4-4FEF-AE9A-25296551ED9DQ42289804-D65104F3-2F6F-435A-88B6-51C02074EE2DQ42654406-68434F78-3D6C-4668-A71E-3048BA22731FQ42829919-8F02CCE8-074E-4D5D-9842-DCFC61B65B75Q43884064-23CA4BF4-932E-46EE-BA04-32518FD6038FQ43903658-DE477301-859B-4C82-92C7-E03E354859D3Q44197150-BF914DD0-9448-4396-AD71-5C093CB3C8BBQ45813740-96A145E3-9A1B-4BB3-8D39-E15C589A8316Q46322498-C55535CD-F77C-4735-BEEC-C0FEC263546AQ46429460-13EC9D35-5F6B-474D-8E5C-B0759DEE4560Q48106774-16530DCB-ADDA-4047-A179-BE9D23D8D4E1Q48152537-E4EF5B0E-EEF3-42E5-9159-028F26E9B80CQ48176404-0E7B0BAD-DCC8-4235-B92B-7F36CA76A149Q48191265-4D368FAC-0BF9-42DE-BD47-340E39F4D34CQ48197707-B47F42FE-B2D1-4780-A11F-68966B911D74Q48199220-C8A04446-1AEE-42FD-8679-ED07CF7A99D0Q48205884-55E05AB9-3668-459F-BFB5-867B11005CE2Q48206048-826B6D93-68AE-40BE-9663-A8706D765A83
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Catalytic selective synthesis.
@en
type
label
Catalytic selective synthesis.
@en
prefLabel
Catalytic selective synthesis.
@en
P2093
P2860
P356
P1476
Catalytic selective synthesis.
@en
P2093
Aaron M Dumas
Jeffrey W Bode
Jessada Mahatthananchai
P2860
P304
10954-10990
P356
10.1002/ANIE.201201787
P407
P577
2012-09-25T00:00:00Z