(Thio)urea organocatalyst equilibrium acidities in DMSO.
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Experimental and Theoretical Studies in Hydrogen-Bonding OrganocatalysisN,N'-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea: a privileged motif for catalyst development.Metal organic frameworks mimicking natural enzymes: a structural and functional analogy.A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst.Rapid quantification of the activating effects of hydrogen-bonding catalysts with a colorimetric sensor.Synthesis of chiral sulfoximine-based thioureas and their application in asymmetric organocatalysis.Quantification of electrophilic activation by hydrogen-bonding organocatalysts.Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement.Xanthene-4,5-diamine derivatives: a study of anion-binding catalysis.Activation of Electron-Deficient Quinones through Hydrogen-Bond-Donor-Coupled Electron TransferCooperative catalysis in glycosidation reactions with O-glycosyl trichloroacetimidates as glycosyl donors.Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.Deltamides and Croconamides: Expanding the Range of Dual H-bond Donors for Selective Anion Recognition.Towards an Observation of Active Conformations in Asymmetric Catalysis: Interaction-Induced Conformational Preferences of a Chiral Thiourea Model Compound.Synthesis of enantioenriched azo compounds: organocatalytic Michael addition of formaldehyde N-tert-butyl hydrazone to nitroalkenes.Study on the Catalytic Behavior of Bifunctional Hydrogen-Bonding Catalysts Guided by Free Energy Relationship Analysis of Steric Parameters.Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction.Asymmetric organocatalytic synthesis of tertiary azomethyl alcohols: key intermediates towards azoxy compounds and α-hydroxy-β-amino esters.Urea- and Thiourea-Catalyzed Aminolysis of Carbonates.Croconamides: a new dual hydrogen bond donating motif for anion recognition and organocatalysis.Ditopic receptors containing urea groups for solvent extraction of Cu(ii) salts.Anion Recognition by Aliphatic Helical Oligoureas.Lewis acid enhancement by hydrogen-bond donors for asymmetric catalysis.Synthesis and evaluation of thiosemicarbazones functionalized with furyl moieties as new chemosensors for anion recognition.Deconstructing covalent organocatalysis.A cooperative hydrogen-bond-promoted organophotoredox catalysis strategy for highly diastereoselective, reductive enone cyclization.Synthesis of deoxynucleoside triphosphates that include proline, urea, or sulfonamide groups and their polymerase incorporation into DNA.Hydrogen-bonding in aminocatalysis: from proline and beyond.Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base.Chirality sensing of tertiary alcohols by a novel strong hydrogen-bonding donor - selenourea.Acidity and basicity interplay in amide and imide self-association.Organocatalytic solvent-free hydrogen bonding-mediated asymmetric Michael additions under ball milling conditionsHydrogen-Bonding Thiourea Organocatalysts: The Privileged 3,5-Bis(trifluoromethyl)phenyl Group
P2860
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P2860
(Thio)urea organocatalyst equilibrium acidities in DMSO.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
(Thio)urea organocatalyst equilibrium acidities in DMSO.
@en
type
label
(Thio)urea organocatalyst equilibrium acidities in DMSO.
@en
prefLabel
(Thio)urea organocatalyst equilibrium acidities in DMSO.
@en
P2093
P356
P1433
P1476
(Thio)urea organocatalyst equilibrium acidities in DMSO.
@en
P2093
Carlo Tancon
Gergely Jakab
Katharina M Lippert
Zhiguo Zhang
P304
P356
10.1021/OL300307C
P407
P577
2012-03-21T00:00:00Z