"On water": unique reactivity of organic compounds in aqueous suspension.
about
A bioorthogonal quadricyclane ligationDiels-Alder cycloadditions in water for the straightforward preparation of peptide-oligonucleotide conjugatesWater and Aqueous Mixtures as Convenient Alternative Media for Organoselenium ChemistryDecreasing Distortion Energies without Strain: Diazo-Selective 1,3-Dipolar CycloadditionsThe unique molecular behavior of water at the chloroform-water interface.Acceleration of reaction in charged microdroplets.Quantum mechanical/molecular mechanical modeling finds Diels-Alder reactions are accelerated less on the surface of water than in water.Strategic redox relay enables a scalable synthesis of ouabagenin, a bioactive cardenolide.Quantum and Molecular Mechanical (QM/MM) Monte Carlo Techniques for Modeling Condensed-Phase Reactions.Mechanism of vibrational energy dissipation of free OH groups at the air-water interface.Palladium(0) catalyzed 2,2'-bipyrrole synthesesMolecular structure and dynamics of water at the water-air interface studied with surface-specific vibrational spectroscopy.Ordered polyelectrolyte assembly at the oil-water interface.Photochemical oxidation of water and reduction of polyoxometalate anions at interfaces of water with ionic liquids or diethyletherA versatile method for the preparation of conjugates of peptides with DNA/PNA/analog by employing chemo-selective click reaction in water.Hydrophobically directed organic synthesis.Organic chemistry in water.Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar caManipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperatureGreen chemistry for chemical synthesis.(+/-)-(1S,2R,5S)-5-Amino-2-fluorocyclohex-3-enecarboxylic acid. A potent GABA aminotransferase inactivator that irreversibly inhibits via an elimination-aromatization pathwayRegioselective synthesis of N-beta-hydroxyethylaziridines by the ring-opening reaction of epoxides with aziridine generated in situArylfluorosulfates Inactivate Intracellular Lipid Binding Protein(s) through Chemoselective SuFEx Reaction with a Binding Site Tyr ResidueEntropic factors provide unusual reactivity and selectivity in epoxide-opening reactions promoted by water.Organic synthesis "on water".Aromatic Claisen Rearrangements of O-prenylated tyrosine and model prenyl aryl ethers: Computational study of the role of water on acceleration of Claisen rearrangements.1,3-Dipolar Cycloaddition with Diazo Groups: Noncovalent Interactions Overwhelm Strain.Environmentally Benign Lewis Acid Promoted [2+3]-Dipolar Cycloaddition Reactions of Nitrile Imines with Alkenes in Water.Acceleration of an aromatic Claisen rearrangement via a designed spiroligozyme catalyst that mimics the ketosteroid isomerase catalytic dyad.The development of aqueous transfer hydrogenation catalysts.Fabrication and functionalization of hydrogels through "click" chemistry.Green chemistry oriented organic synthesis in water.Making expensive dirhodium(II) catalysts cheaper: Rh(II) recycling methods.Recent efforts directed to the development of more sustainable asymmetric organocatalysis.N-Heterocyclic carbene transition metal complexes for catalysis in aqueous media.Solvent-free and catalysts-free chemistry: a benign pathway to sustainability.Transitioning organic synthesis from organic solvents to water. What's your E Factor?2-Alkynylbenzaldoxime: a versatile building block for the generation of N-heterocycles.Efficient Conjugation of Oligosaccharides to Polymer Particles through Furan/Maleimide Diels-Alder Reaction: Application to the Capture of Carbohydrate-Binding Proteins.C-C bond formation via copper-catalyzed conjugate addition reactions to enones in water at room temperature
P2860
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P2860
"On water": unique reactivity of organic compounds in aqueous suspension.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
"On water": unique reactivity of organic compounds in aqueous suspension.
@ast
"On water": unique reactivity of organic compounds in aqueous suspension.
@en
"On water": unique reactivity of organic compounds in aqueous suspension.
@nl
type
label
"On water": unique reactivity of organic compounds in aqueous suspension.
@ast
"On water": unique reactivity of organic compounds in aqueous suspension.
@en
"On water": unique reactivity of organic compounds in aqueous suspension.
@nl
prefLabel
"On water": unique reactivity of organic compounds in aqueous suspension.
@ast
"On water": unique reactivity of organic compounds in aqueous suspension.
@en
"On water": unique reactivity of organic compounds in aqueous suspension.
@nl
P2093
P50
P356
P1476
"On water": unique reactivity of organic compounds in aqueous suspension.
@en
P2093
Hartmuth C Kolb
John Muldoon
Sridhar Narayan
P304
P356
10.1002/ANIE.200462883
P407
P577
2005-05-01T00:00:00Z