Published in Science on September 28, 2007
Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis. Chem Rev (2013) 5.62
Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides. Science (2009) 4.13
A medicinal chemist's guide to molecular interactions. J Med Chem (2010) 3.39
Enantioselective alpha-trifluoromethylation of aldehydes via photoredox organocatalysis. J Am Chem Soc (2009) 2.98
The palladium-catalyzed trifluoromethylation of aryl chlorides. Science (2010) 2.85
Catalysis for fluorination and trifluoromethylation. Nature (2011) 2.70
Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways. Science (2013) 2.31
Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis. Nature (2011) 2.30
Antidepressant specificity of serotonin transporter suggested by three LeuT-SSRI structures. Nat Struct Mol Biol (2009) 2.12
Merging visible-light photocatalysis and transition-metal catalysis in the copper-catalyzed trifluoromethylation of boronic acids with CF3I. J Am Chem Soc (2012) 1.86
Practical and innate carbon-hydrogen functionalization of heterocycles. Nature (2012) 1.83
Mechanism of C-F reductive elimination from palladium(IV) fluorides. J Am Chem Soc (2010) 1.83
Silver-catalyzed late-stage fluorination. J Am Chem Soc (2010) 1.62
Copper-catalyzed arylation and alkenylation of polyfluoroarene C-H bonds. J Am Chem Soc (2008) 1.61
Selective neuronal nitric oxide synthase inhibitors and the prevention of cerebral palsy. Ann Neurol (2009) 1.58
Room temperature aryl trifluoromethylation via copper-mediated oxidative cross-coupling. J Org Chem (2011) 1.52
Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides. J Am Chem Soc (2011) 1.47
High-valent organometallic copper and palladium in catalysis. Nature (2012) 1.46
Fluorinated Cannabidiol Derivatives: Enhancement of Activity in Mice Models Predictive of Anxiolytic, Antidepressant and Antipsychotic Effects. PLoS One (2016) 1.40
Investigating the Influence of (Deoxy)fluorination on the Lipophilicity of Non-UV-Active Fluorinated Alkanols and Carbohydrates by a New log P Determination Method. Angew Chem Int Ed Engl (2015) 1.40
Engineering fluorometabolite production: fluorinase expression in Salinispora tropica Yields Fluorosalinosporamide. J Nat Prod (2010) 1.39
The C-F bond as a conformational tool in organic and biological chemistry. Beilstein J Org Chem (2010) 1.34
Fe(III)/NaBH4-mediated free radical hydrofluorination of unactivated alkenes. J Am Chem Soc (2012) 1.33
Structural insights into inhibition of the bivalent menin-MLL interaction by small molecules in leukemia. Blood (2012) 1.31
The productive merger of iodonium salts and organocatalysis: a non-photolytic approach to the enantioselective alpha-trifluoromethylation of aldehydes. J Am Chem Soc (2010) 1.29
Pd-catalyzed nucleophilic fluorination of aryl bromides. J Am Chem Soc (2014) 1.28
Advances in catalytic enantioselective fluorination, mono-, di-, and trifluoromethylation, and trifluoromethylthiolation reactions. Chem Rev (2014) 1.28
An improved catalyst system for the Pd-catalyzed fluorination of (hetero)aryl triflates. Org Lett (2013) 1.24
Protein flexibility and conformational entropy in ligand design targeting the carbohydrate recognition domain of galectin-3. J Am Chem Soc (2010) 1.24
A perfluoroaryl-cysteine S(N)Ar chemistry approach to unprotected peptide stapling. J Am Chem Soc (2013) 1.23
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity. ACS Med Chem Lett (2014) 1.23
Chemo-enzymatic fluorination of unactivated organic compounds. Nat Chem Biol (2008) 1.23
Salinosporamide natural products: Potent 20 S proteasome inhibitors as promising cancer chemotherapeutics. Angew Chem Int Ed Engl (2010) 1.22
Halogenated beta,gamma-methylene- and ethylidene-dGTP-DNA ternary complexes with DNA polymerase beta: structural evidence for stereospecific binding of the fluoromethylene analogues. J Am Chem Soc (2010) 1.21
Accelerating palladium-catalyzed C-F bond formation: use of a microflow packed-bed reactor. Angew Chem Int Ed Engl (2011) 1.18
Photoredox catalysis: a mild, operationally simple approach to the synthesis of α-trifluoromethyl carbonyl compounds. Angew Chem Int Ed Engl (2011) 1.15
Standard protecting groups create potent and selective kappa opioids: salvinorin B alkoxymethyl ethers. Bioorg Med Chem (2007) 1.15
Structural evaluation of potent NKT cell agonists: implications for design of novel stimulatory ligands. J Mol Biol (2009) 1.13
Molecular imaging probe development: a chemistry perspective. Am J Nucl Med Mol Imaging (2012) 1.10
A general strategy for the perfluoroalkylation of arenes and arylbromides by using arylboronate esters and [(phen)CuR(F)]. Angew Chem Int Ed Engl (2011) 1.09
Practical method for the Cu-mediated trifluoromethylation of arylboronic acids with CF3 radicals derived from NaSO2CF3 and tert-butyl hydroperoxide (TBHP). Org Lett (2012) 1.07
Structure based development of phenylimidazole-derived inhibitors of indoleamine 2,3-dioxygenase. J Med Chem (2008) 1.07
A broadly applicable [18F]trifluoromethylation of aryl and heteroaryl iodides for PET imaging. Nat Chem (2013) 1.03
Application of palladium-mediated (18)F-fluorination to PET radiotracer development: overcoming hurdles to translation. PLoS One (2013) 1.03
Copper-catalyzed trifluoromethylation of unactivated olefins. Angew Chem Int Ed Engl (2011) 1.03
The palladium-catalyzed trifluoromethylation of vinyl sulfonates. Org Lett (2011) 1.02
New frontiers and developing applications in 19F NMR. Prog Nucl Magn Reson Spectrosc (2012) 1.02
Enantioselective organocatalytic α-fluorination of cyclic ketones. J Am Chem Soc (2011) 1.02
Exhaustive fluorine scanning toward potent p53-Mdm2 antagonists. ChemMedChem (2011) 1.01
Visible light-promoted metal-free C-H activation: diarylketone-catalyzed selective benzylic mono- and difluorination. J Am Chem Soc (2013) 1.01
Fluorine substitutions in an antigenic peptide selectively modulate T-cell receptor binding in a minimally perturbing manner. Biochem J (2009) 1.00
Steric Crowding Makes Challenging C(sp3)-F Reductive Eliminations Feasible. Organometallics (2011) 1.00
Synthesis of polyfluoro ketones for selective inhibition of human phospholipase A2 enzymes. J Med Chem (2008) 0.99
Asymmetric fluorination of α-branched cyclohexanones enabled by a combination of chiral anion phase-transfer catalysis and enamine catalysis using protected amino acids. J Am Chem Soc (2014) 0.98
Incorporation of fluorotyrosines into ribonucleotide reductase using an evolved, polyspecific aminoacyl-tRNA synthetase. J Am Chem Soc (2011) 0.98
A novel mechanism by which small molecule inhibitors induce the DFG flip in Aurora A. ACS Chem Biol (2012) 0.98
Potent and selective fluoroketone inhibitors of group VIA calcium-independent phospholipase A2. J Med Chem (2010) 0.97
Isoform-specific prolongation of Kv7 (KCNQ) potassium channel opening mediated by new molecular determinants for drug-channel interactions. J Biol Chem (2010) 0.97
Chemoenzymatic elaboration of monosaccharides using engineered cytochrome P450BM3 demethylases. Proc Natl Acad Sci U S A (2009) 0.96
Fluorine modulates species selectivity in the triazolopyrimidine class of Plasmodium falciparum dihydroorotate dehydrogenase inhibitors. J Med Chem (2014) 0.96
Rapid and efficient trifluoromethylation of aromatic and heteroaromatic compounds using potassium trifluoroacetate enabled by a flow system. Angew Chem Int Ed Engl (2013) 0.95
Sugar nucleotide recognition by Klebsiella pneumoniae UDP-D-galactopyranose mutase: fluorinated substrates, kinetics and equilibria. Org Biomol Chem (2009) 0.95
Late-stage deoxyfluorination of alcohols with PhenoFluor. J Am Chem Soc (2013) 0.95
Decarboxylative Fluorination of Aliphatic Carboxylic Acids via Photoredox Catalysis. J Am Chem Soc (2015) 0.94
Proline editing: a general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4-substituted prolines on conformation within peptides. J Am Chem Soc (2013) 0.94
Designer HF-based fluorination reagent: highly regioselective synthesis of fluoroalkenes and gem-difluoromethylene compounds from alkynes. J Am Chem Soc (2014) 0.94
Optimization of adenosine 5'-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screening. J Med Chem (2012) 0.93
Prins fluorination cyclisations: Preparation of 4-fluoro-pyran and -piperidine heterocycles. Beilstein J Org Chem (2010) 0.93
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the "hydrophobic wall" of carbonic anhydrase. J Am Chem Soc (2011) 0.93
Use of Fluorinated Functionality in Enzyme Inhibitor Development: Mechanistic and Analytical Advantages. J Fluor Chem (2008) 0.92
Asymmetric synthesis of trifluoromethylated amines via catalytic enantioselective isomerization of imines. J Am Chem Soc (2012) 0.92
Crystal structures of HIV-1 gp120 envelope glycoprotein in complex with NBD analogues that target the CD4-binding site. PLoS One (2014) 0.91
Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers. Org Lett (2013) 0.91
Colocalization of the ganglioside G(M1) and cholesterol detected by secondary ion mass spectrometry. J Am Chem Soc (2013) 0.91
Silver-mediated trifluoromethoxylation of aryl stannanes and arylboronic acids. J Am Chem Soc (2011) 0.91
Electrophilic fluorination of cationic Pt-aryl complexes. Chem Commun (Camb) (2011) 0.90
Synthesis of fluorinated benzophenones, xanthones, acridones, and thioxanthones by iterative nucleophilic aromatic substitution. J Org Chem (2011) 0.90
Structural and biochemical studies of a fluoroacetyl-CoA-specific thioesterase reveal a molecular basis for fluorine selectivity. Biochemistry (2010) 0.90
An ultrahigh affinity d-peptide antagonist Of MDM2. J Med Chem (2012) 0.90
Discovery of GSK2656157: An Optimized PERK Inhibitor Selected for Preclinical Development. ACS Med Chem Lett (2013) 0.90
Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (α-trifluoromethyl)allylation from the alcohol or aldehyde oxidation level. Angew Chem Int Ed Engl (2011) 0.90
Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates. Angew Chem Int Ed Engl (2012) 0.90
Hydration dynamics at fluorinated protein surfaces. Proc Natl Acad Sci U S A (2010) 0.89
C-F Bond Formation for the Synthesis of Aryl Fluorides. Synthesis (Stuttg) (2010) 0.89
C(sp(3))-F reductive elimination from alkylgold(iii) fluoride complexes. Chem Sci (2011) 0.89
Catalytic enantioselective cyclization and C3-fluorination of polyenes. J Am Chem Soc (2013) 0.88
Development of a novel class of glucose transporter inhibitors. J Med Chem (2012) 0.88
Silver-mediated trifluoromethylation of arenes using TMSCF3. Org Lett (2011) 0.88
Small molecules showing significant protection of mice against botulinum neurotoxin serotype A. PLoS One (2010) 0.88
Synthesis and preliminary pharmacological evaluation of novel derivatives of L-beta-threo-benzylaspartate as inhibitors of the neuronal glutamate transporter EAAT3. Bioorg Med Chem (2008) 0.88
Separation of Fluorinated Amino Acids and Oligopeptides from their Non-fluorinated Counterparts using High-performance Liquid Chromatography. J Fluor Chem (2010) 0.88
Structural basis for the enhanced stability of highly fluorinated proteins. Proc Natl Acad Sci U S A (2012) 0.88
Investigations into Transition Metal Catalyzed Arene Trifluoromethylation Reactions. Synlett (2012) 0.88
The difluoromethylene (CF2) group in aliphatic chains: Synthesis and conformational preference of palmitic acids and nonadecane containing CF2 groups. Beilstein J Org Chem (2014) 0.87
Exploration of fluorine chemistry at the multidisciplinary interface of chemistry and biology. J Org Chem (2013) 0.87
Dosage delivery of sensitive reagents enables glove-box-free synthesis. Nature (2015) 0.87
Late-Stage Fluorination: From Fundamentals to Application. Org Process Res Dev (2014) 0.87
A beta-fluoroamine inhibitor of purine nucleoside phosphorylase. J Med Chem (2008) 0.86
Development of new deoxycytidine kinase inhibitors and noninvasive in vivo evaluation using positron emission tomography. J Med Chem (2013) 0.86
Interactions with aromatic rings in chemical and biological recognition. Angew Chem Int Ed Engl (2003) 5.63
Aromatic rings in chemical and biological recognition: energetics and structures. Angew Chem Int Ed Engl (2011) 2.48
Systematic investigation of halogen bonding in protein-ligand interactions. Angew Chem Int Ed Engl (2011) 1.54
Orthogonal multipolar interactions in structural chemistry and biology. Angew Chem Int Ed Engl (2005) 1.54
Predicting and tuning physicochemical properties in lead optimization: amine basicities. ChemMedChem (2007) 1.48
The pleasure and importance of printed journals. Nature (2009) 1.39
Molecular recognition in chemical and biological systems. Angew Chem Int Ed Engl (2015) 1.28
Quantification of cation-pi interactions in protein-ligand complexes: crystal-structure analysis of Factor Xa bound to a quaternary ammonium ion ligand. Angew Chem Int Ed Engl (2005) 1.20
Structural aspects of fullerene chemistry--a journey through fullerene chirality. Chem Rev (2006) 1.17
Phosphate recognition in structural biology. Angew Chem Int Ed Engl (2007) 1.17
Regio- and stereoselective tether-directed remote functionalization of C60 with derivatives of the Tröger base. Angew Chem Int Ed Engl (2004) 1.15
Steroids in Molecular Recognition. Chem Rev (1997) 1.09
Expanding the chemical space for push-pull chromophores by non-concerted [2+2] and [4+2] cycloadditions: access to a highly functionalised 6,6-dicyanopentafulvene with an intense, low-energy charge-transfer band. Chem Commun (Camb) (2011) 1.06
Fluorine interactions at the thrombin active site: protein backbone fragments H-C(alpha)-C=O comprise a favorable C-F environment and interactions of C-F with electrophiles. Chembiochem (2004) 0.99
Container molecules with portals: Reversibly switchable cycloalkane complexation. Angew Chem Int Ed Engl (2007) 0.99
Modification of supramolecular binding motifs induced by substrate registry: formation of self-assembled macrocycles and chain-like patterns. Chemistry (2009) 0.97
Amphiphilic dendrimers: novel self-assembling vectors for efficient gene delivery. Angew Chem Int Ed Engl (2003) 0.96
Orthogonal dipolar interactions between amide carbonyl groups. Proc Natl Acad Sci U S A (2008) 0.95
Structure-based drug design: exploring the proper filling of apolar pockets at enzyme active sites. J Org Chem (2008) 0.95
Allenes in molecular materials. Angew Chem Int Ed Engl (2012) 0.95
Pentafluorosulfanyl as a novel building block for enzyme inhibitors: trypanothione reductase inhibition and antiprotozoal activities of diarylamines. Chembiochem (2009) 0.94
Supramolecular patterned surfaces driven by cooperative assembly of C60 and porphyrins on metal substrates. Angew Chem Int Ed Engl (2004) 0.93
Geometrically precisely defined multinanometer expansion/contraction motions in a resorcin[4]arene cavitand based molecular switch. Angew Chem Int Ed Engl (2005) 0.93
A fluorine scan of the phenylamidinium needle of tricyclic thrombin inhibitors: effects of fluorine substitution on pKa and binding affinity and evidence for intermolecular C-F...CN interactions. Org Biomol Chem (2004) 0.93
A weak attractive interaction between organic fluorine and an amide group. Angew Chem Int Ed Engl (2004) 0.92
Cation-pi interactions at the active site of factor Xa: dramatic enhancement upon stepwise N-alkylation of ammonium ions. Angew Chem Int Ed Engl (2009) 0.92
Crystal structures of tRNA-guanine transglycosylase (TGT) in complex with novel and potent inhibitors unravel pronounced induced-fit adaptations and suggest dimer formation upon substrate binding. J Mol Biol (2007) 0.91
A fluorine scan of thrombin inhibitors to map the fluorophilicity/fluorophobicity of an enzyme active site: evidence for C-F...C=O interactions. Angew Chem Int Ed Engl (2003) 0.90
Directed rotations of single porphyrin molecules controlled by localized force spectroscopy. ACS Nano (2012) 0.89
Inhibitors of the herbicidal target IspD: allosteric site binding. Angew Chem Int Ed Engl (2011) 0.88
The state of the art of chemical biology. Chembiochem (2009) 0.88
Improved inhibitors of trypanothione reductase by combination of motifs: synthesis, inhibitory potency, binding mode, and antiprotozoal activities. ChemMedChem (2010) 0.88
Starving the malaria parasite: inhibitors active against the aspartic proteases plasmepsins I, II, and IV. Angew Chem Int Ed Engl (2006) 0.87
Conjugated oligoenynes based on the diethynylethene unit. Chem Rev (2005) 0.87
Efficient stacking on protein amide fragments. ChemMedChem (2013) 0.87
Supramolecular [60]fullerene chemistry on surfaces. Chem Soc Rev (2006) 0.87
Property tuning in charge-transfer chromophores by systematic modulation of the spacer between donor and acceptor. Chemistry (2007) 0.87
Molecular torsion balances: evidence for favorable orthogonal dipolar interactions between organic fluorine and amide groups. Angew Chem Int Ed Engl (2007) 0.87
From lin-benzoguanines to lin-benzohypoxanthines as ligands for Zymomonas mobilis tRNA-guanine transglycosylase: replacement of protein-ligand hydrogen bonding by importing water clusters. Chemistry (2012) 0.87
Calculation of binding free energies of inhibitors to plasmepsin II. J Comput Chem (2011) 0.85
Molecular recognition at the active site of factor Xa: cation-π interactions, stacking on planar peptide surfaces, and replacement of structural water. Chemistry (2011) 0.85
Triply fused Zn(II)-porphyrin oligomers: synthesis, properties, and supramolecular interactions with single-walled carbon nanotubes (SWNTs). Chemistry (2006) 0.84
Halogen bonding of (iodoethynyl)benzene derivatives in solution. Org Lett (2014) 0.84
A fluorine scan at the catalytic center of thrombin: C--F, C--OH, and C--OMe bioisosterism and fluorine effects on pKa and log D values. ChemMedChem (2006) 0.84
Fluorescent inhibitors for IspF, an enzyme in the non-mevalonate pathway for isoprenoid biosynthesis and a potential target for antimalarial therapy. Angew Chem Int Ed Engl (2006) 0.84
Nonphosphate inhibitors of IspE protein, a kinase in the non-mevalonate pathway for isoprenoid biosynthesis and a potential target for antimalarial therapy. ChemMedChem (2007) 0.83
A supramolecular multiposition rotary device. Angew Chem Int Ed Engl (2007) 0.83
Thiazolopyrimidine inhibitors of 2-methylerythritol 2,4-cyclodiphosphate synthase (IspF) from Mycobacterium tuberculosis and Plasmodium falciparum. ChemMedChem (2010) 0.83
Potent and selective inhibition of cysteine proteases from Plasmodium falciparum and Trypanosoma brucei. ChemMedChem (2010) 0.83
Cryogenic 35GHz pulse ENDOR probehead accommodating large sample sizes: Performance and applications. J Magn Reson (2009) 0.83
Nanoscale engineering of molecular porphyrin wires on insulating surfaces. Small (2008) 0.83
Molecular recognition at the active site of catechol-o-methyltransferase: energetically favorable replacement of a water molecule imported by a bisubstrate inhibitor. Angew Chem Int Ed Engl (2009) 0.83
Shape-persistent chiral alleno-acetylenic macrocycles and cyclophanes by acetylenic scaffolding with 1,3-diethynylallenes. Angew Chem Int Ed Engl (2005) 0.83
Synthesis and characterization of cytidine derivatives that inhibit the kinase IspE of the non-mevalonate pathway for isoprenoid biosynthesis. ChemMedChem (2008) 0.83
Molecular recognition at the active site of catechol-O-methyltransferase (COMT): adenine replacements in bisubstrate inhibitors. Chemistry (2011) 0.82
Acetylene-derived strong organic acceptors for planar and nonplanar push-pull chromophores. Acc Chem Res (2009) 0.82
Halogen bonding at the active sites of human cathepsin L and MEK1 kinase: efficient interactions in different environments. ChemMedChem (2011) 0.82
1,2,3-triazoles as conjugative pi-linkers in push-pull chromophores: importance of substituent positioning on intramolecular charge-transfer. Org Lett (2008) 0.82
Inhibitors of the kinase IspE: structure-activity relationships and co-crystal structure analysis. Org Biomol Chem (2008) 0.82
Diaryl sulfide-based inhibitors of trypanothione reductase: inhibition potency, revised binding mode and antiprotozoal activities. Org Biomol Chem (2008) 0.82
Two-dimensional acetylenic scaffolding: extended donor-substituted perethynylated dehydroannulenes. Chem Asian J (2006) 0.82
One-electron-reduced and -oxidized stages of donor-substituted 1,1,4,4-tetracyanobuta-1,3-dienes of different molecular architectures. Chemistry (2008) 0.81
Structures and stabilities of diacetylene-expanded polyhedranes by quantum mechanics and molecular mechanics. J Org Chem (2005) 0.81
PROLIX: rapid mining of protein-ligand interactions in large crystal structure databases. J Chem Inf Model (2012) 0.81
Synthesis, inhibition potency, binding mode, and antiprotozoal activities of fluorescent inhibitors of trypanothione reductase based on mepacrine-conjugated diaryl sulfide scaffolds. ChemMedChem (2009) 0.81
A new class of organic donor-acceptor molecules with large third-order optical nonlinearities. Chem Commun (Camb) (2005) 0.81
How to replace the residual solvation shell of polar active site residues to achieve nanomolar inhibition of tRNA-guanine transglycosylase. ChemMedChem (2009) 0.81
High-affinity inhibitors of tRNA-guanine transglycosylase replacing the function of a structural water cluster. Chemistry (2009) 0.81
Bisubstrate inhibitors for the enzyme catechol-O-methyltransferase (COMT): influence of inhibitor preorganisation and linker length between the two substrate moieties on binding affinity. Org Biomol Chem (2003) 0.81
Regio- and diastereoselective synthesis of bis- and tetrakisadducts of C70 by directed remote functionalization using Tröger base tethers. Chemistry (2006) 0.81
Pseudilins: halogenated, allosteric inhibitors of the non-mevalonate pathway enzyme IspD. Angew Chem Int Ed Engl (2014) 0.81
De novo design, synthesis, and in vitro evaluation of inhibitors for prokaryotic tRNA-guanine transglycosylase: a dramatic sulfur effect on binding affinity. Chembiochem (2002) 0.81
Launching spiking ligands into a protein-protein interface: a promising strategy to destabilize and break interface formation in a tRNA modifying enzyme. ACS Chem Biol (2013) 0.80
Charge-transfer chromophores by cycloaddition-retro-electrocyclization: multivalent systems and cascade reactions. Angew Chem Int Ed Engl (2007) 0.80
Tuning and predicting biological affinity: aryl nitriles as cysteine protease inhibitors. Org Biomol Chem (2012) 0.80
Resonant tunnelling through a C(60) molecular junction in a liquid environment. Nanotechnology (2005) 0.80
Free enthalpies of replacing water molecules in protein binding pockets. J Comput Aided Mol Des (2012) 0.80
Donor-substituted cyanoethynylethenes: powerful chromophores for opto-electronic applications. Org Biomol Chem (2003) 0.79
Conformational behavior of pyrazine-bridged and mixed-bridged cavitands: a general model for solvent effects on thermal "vase-kite" switching. Chemistry (2006) 0.79
Optical properties of highly nonlinear silicon-organic hybrid (SOH) waveguide geometries. Opt Express (2009) 0.79
Peralkynylated buta-1,2,3-trienes: exceptionally low rotational barriers of cumulenic C=C bonds in the range of those of peptide C--N bonds. Chemistry (2004) 0.79
FRET studies on a series of BODIPY-dye-labeled switchable resorcin[4]arene cavitands. Chemistry (2010) 0.79
New donor-acceptor chromophores by formal [2+2] cycloaddition of donor-substituted alkynes to dicyanovinyl derivatives. Org Biomol Chem (2009) 0.79
A novel reaction of 7,7,8,8-tetracyanoquinodimethane (TCNQ): charge-transfer chromophores by [2 + 2] cycloaddition with alkynes. Chem Commun (Camb) (2007) 0.79
Effects of the dendrimer cage on O2 binding of dendritic cobalt(II) porphyrins. Chemphyschem (2002) 0.79
Crystallographic study of inhibitors of tRNA-guanine transglycosylase suggests a new structure-based pharmacophore for virtual screening. J Mol Biol (2004) 0.79
1,3-Diethynylallenes (DEAs): enantioselective synthesis, absolute configuration, and chiral induction in 1,1,4,4-tetracyanobuta-1,3-dienes (TCBDs). Chemistry (2008) 0.79
Experimental and computational study of BODIPY dye-labeled cavitand dynamics. J Am Chem Soc (2014) 0.79
Crystal structure analysis and in silico pKa calculations suggest strong pKa shifts of ligands as driving force for high-affinity binding to TGT. Chembiochem (2009) 0.79
Binding to large enzyme pockets: small-molecule inhibitors of trypanothione reductase. ChemMedChem (2014) 0.78
Bisubstrate inhibitors of catechol O-methyltransferase (COMT): the crucial role of the ribose structural unit for inhibitor binding affinity. ChemMedChem (2006) 0.78
Self-assembly and two-dimensional spontaneous resolution of cyano-functionalized [7]helicenes on Cu111. Angew Chem Int Ed Engl (2011) 0.78
Supramolecular synthons on surfaces: controlling dimensionality and periodicity of tetraarylporphyrin assemblies by the interplay of cyano and alkoxy substituents. Chemistry (2008) 0.78
Betraying the parasite's redox system: diaryl sulfide-based inhibitors of trypanothione reductase: subversive substrates and antitrypanosomal properties. ChemMedChem (2007) 0.78
Photophysical and electrochemical properties of meso, meso-linked oligoporphyrin rods with appended fullerene terminals. Chemphyschem (2005) 0.78
Quinone-based, redox-active resorcin[4]arene cavitands. Angew Chem Int Ed Engl (2011) 0.78
Optical stability of axially chiral push-pull-substituted buta-1,3-dienes: effect of a single methyl group on the C60 surface. Angew Chem Int Ed Engl (2010) 0.78
Medicinal chemistry in academia: molecular recognition with biological receptors. Chem Commun (Camb) (2004) 0.78
Multipolar interactions in the D pocket of thrombin: large differences between tricyclic imide and lactam inhibitors. Org Biomol Chem (2006) 0.78