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- 2012
-
Mark
Selective mode of action of guanidine-containing non-peptides at human NPFF receptors
(
- Contribution to journal › Article
-
Mark
Discovery of potential antipsychotic agents possessing pro-cognitive properties
(
- Contribution to journal › Article
- 2011
-
Mark
Can alpha-synuclein be targeted in novel therapies for Parkinson's disease?
(
- Contribution to journal › Article
-
Mark
Reactions between Grignard reagents and heterocyclic N-oxides : Stereoselective synthesis of substituted pyridines, piperidines, and piperazines
(
- Contribution to journal › Scientific review
-
Mark
Characterization of highly efficacious allosteric agonists of the human calcium-sensing receptor
(
- Contribution to journal › Article
- 2010
-
Mark
Asymmetric synthesis of a tricyclic benzofuran motif : A privileged core structure in biologically active molecules
(
- Contribution to journal › Article
-
Mark
Synthesis of substituted 4-pyridones and 4-aminopyridinium salts via a one-pot pyridine synthesis
(
- Contribution to journal › Article
-
Mark
Efficient, mild and completely regioselective synthesis of substituted pyridines
(
- Contribution to journal › Article
-
Mark
Complete regioselective addition of grignard reagents to pyrazine N-oxides, toward an efficient enantioselective synthesis of substituted piperazines
(
- Contribution to journal › Article
-
Mark
Optimization of isochromanone based urotensin II receptor agonists
(
- Contribution to journal › Article
-
Mark
Discovery of a class of calcium sensing receptor positive allosteric modulators; 1-(benzothiazol-2-yl)-1-phenylethanols
(
- Contribution to journal › Article
-
Mark
Neuropeptide FF receptors have opposing modulatory effects on nociception
(
- Contribution to journal › Article
- 2009
-
Mark
The regio- and stereoselective synthesis of trans-2,3-dihydropyridine n-oxides and piperidines
(
- Contribution to journal › Article
-
Mark
Discovery of non-peptidergic MrgX1 and MrgX2 receptor agonists and exploration of an initial SAR using solid-phase synthesis
(
- Contribution to journal › Article
-
Mark
Novel and potent small-molecule urotensin II receptor agonists
(
- Contribution to journal › Article
-
Mark
Design, synthesis, and structure-activity analysis of isoform-selective retinoic acid receptor β ligands
(
- Contribution to journal › Article
-
Mark
Discovery of selective nonpeptidergic neuropeptide FF2 receptor agonists
(
- Contribution to journal › Article
-
Mark
Synthesis, structure-activity relationships, and characterization of novel nonsteroidal and selective androgen receptor modulators
(
- Contribution to journal › Article
-
Mark
Synthesis and evaluation of dibenzothiazepines : A novel class of selective cannabinoid-1 receptor inverse agonists
(
- Contribution to journal › Article
- 2008
-
Mark
Selective synthesis of 2-substituted pyridine N-oxides via directed ortho-metallation using Grignard reagents
(
- Contribution to journal › Article
-
Mark
Discovery of potent and selective small-molecule PAR-2 agonists
(
- Contribution to journal › Article
-
Mark
Identification of the first synthetic steroidogenic factor 1 inverse agonists : Pharmacological modulation of steroidogenic enzymes
(
- Contribution to journal › Article
-
Mark
Pharmacological characterization of AC-262536, a novel selective androgen receptor modulator
(
- Contribution to journal › Article
-
Mark
Differential modulation of inflammatory pain by a selective estrogen receptor beta agonist
(
- Contribution to journal › Article
-
Mark
Identification of novel selective V2 receptor non-peptide agonists
(
- Contribution to journal › Article
-
Mark
Broad modulation of neuropathic pain states by a selective estrogen receptor beta agonist
(
- Contribution to journal › Article
-
Mark
Identification and characterization of novel small-molecule protease-activated receptor 2 agonists
(
- Contribution to journal › Article
- 2007
-
Mark
Synthesis of 2-substituted pyridines via a regiospecific alkylation, alkynylation, and arylation of pyridine N-oxides
(
- Contribution to journal › Article
-
Mark
Reaction of pyridine N-oxides with Grignard reagents : a stereodefined synthesis of substituted dienal oximes
(
- Contribution to journal › Article
-
Mark
Design, parallel synthesis and SAR of novel urotensin II receptor agonists
(
- Contribution to journal › Article
-
Mark
Identification of the atypical L-type Ca2+ channel blocker diltiazem and its metabolites as ghrelin receptor agonists
(
- Contribution to journal › Article
-
Mark
Pharmacology and signaling properties of epidermal growth factor receptor isoforms studied by bioluminescence resonance energy transfer
(
- Contribution to journal › Article
- 2006
-
Mark
Iron-catalyzed cross-coupling of imidoyl chlorides with Grignard reagents
(
- Contribution to journal › Article
-
Mark
Novel potent and efficacious nonpeptidic urotensin II receptor agonists
(
- Contribution to journal › Article
- 2005
-
Mark
Isochromanone-based urotensin-II receptor agonists
(
- Contribution to journal › Article
-
Mark
Discovery of a potent, orally available, and isoform-selective retinoic acid β2 receptor agonist
(
- Contribution to journal › Article
-
Mark
Identification of novel subtype selective RAR agonists
(
- Contribution to journal › Article
- 2003
-
Mark
A combinatorial scaffold approach based upon a multicomponent reaction
(
- Contribution to journal › Article
-
Mark
Efficient Solution-Phase Parallel Synthesis of 4-Substituted N-Protected Piperidines
(
- Contribution to journal › Article
-
Mark
Solution-phase parallel Wittig olefination : Synthesis of substituted 1,2-diarylethanes
(
- Contribution to journal › Article
- 2002
-
Mark
A Novel Metal Iodide Promoted Three-Component Synthesis of Substituted Pyrrolidines
(
- Contribution to journal › Article
-
Mark
One-pot three-component reaction for the synthesis of α-(aminoethyl)-α,β-enones
(
- Contribution to journal › Article
-
Mark
Discovery of the first nonpeptide agonist of the GPR14/Urotensin-II receptor : 3-(4-Chlorophenyl)-3-(2-(dimethylamino)ethyl)isochroman-1-one (AC-7954)
(
- Contribution to journal › Article
- 2001
-
Mark
General combinatorial synthesis of tertiary amines on solid support. A novel conditional release strategy based on traceless linking at nitrogen
(
- Contribution to journal › Article
- 2000
-
Mark
Temporary in situ aluminum and zinc tethering in Diels-Alder reactions
(
- Contribution to journal › Article
-
Mark
Multistep solution-phase parallel synthesis of spiperone analogues
(
- Contribution to journal › Article
- 1998
-
Mark
Alkylative cleavage of the endo-cyclic C-O bond in lactol ethers employing organometallic reagents
(
- Contribution to journal › Article
-
Mark
Chelation-controlled regioselective endo cleavage and stereoselective C-1 alkylation of pentofuranosides
(
- Contribution to journal › Article
-
Mark
Endocyclic cleavage of glycosides. VI. Substituent effects of the alkylative endocyclic cleavage of glycosides
(
- Contribution to journal › Article
-
Mark
Organotitanium-induced stereoselective alkylative endo-cleavage of benzyl pentopyranosides
(
- Contribution to journal › Article