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Alpha 1a adrenergic receptor antagonist
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Method for preparing chiral diphosphines
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The metabolic and biochemical impact of glucose 6-sulfonate (sulfoquinovose), a dietary sugar, on carbohydrate metabolism
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Carbohydrate Research p. 21 - 29
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Nematicidal alkenanilides
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Electrolytic Partial Fluorination of Organic Compounds. 24.1 Highly Regioselective Anodic Monofluorination of 2-Benzothiazolyl and 5-Chloro-2-benzothiazolyl Sulfides
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NOVEL ETHYLENEDIAMINE DERIVATIVES
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2-substituted (2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1- yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2. Effects of aromatic substitution, pharmacological characterization, and bioavailability
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Journal of Medicinal Chemistry p. 358 - 378
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Molecular cobalt-salen complexes as novel cocatalysts for highly efficient photocatalytic hydrogen production over a CdS nanorod photosensitizer under visible light
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Antihypertensive 2-amino-4(3H)-quinazolinones.
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Journal of medicinal chemistry p. 130 - 136
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1,7-dithioxo systems. Reaction of 3-[(5,5-dimethyl-3-thioxocyclohex-1-en-1yl)sulfanyl]-5,5-dimethylcyclohex-2-ene-1-thione with 2-aminoethanol and ethane-1,2-diamine
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Russian Journal of Organic Chemistry p. 1795 - 1798
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PROCESS FOR PRODUCTION OF 2-CYANO-3-HYDROXY-N-(4-TRI- FLUOROMETHYLPHENYL)HEPT-2-EN-6-YNAMIDE AND PROCESS FOR PRODUCTION OF POLYMORPHS THEREOF
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Discovery of SB-705498: A potent, selective and orally bioavailable TRPV1 antagonist suitable for clinical development
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Bioorganic and Medicinal Chemistry Letters p. 3287 - 3291
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Synthesis and characterization of flavin-tethered peptide nucleic acid
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Tetrahedron Letters p. 2529 - 2531
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SWERN OXIDATION OF α-KETOLS TO α-DIKETONES
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Synthetic Communications p. 777 - 786
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AZOLE-FUSED PYRIDAZIN-3(2H)-ONE DERIVATIVES
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Lessons in Strain and Stability: Enantioselective Synthesis of (+)-[5]-Ladderanoic Acid
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Angewandte Chemie - International Edition p. 436 - 441
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HETEROCYCLIC INHIBITORS OF MCT4
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Base catalyzed cyclization of N-aryl and N-alkyl-O-propargyl carbamates to 4-alkylidene-2-oxazolidinones
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Tetrahedron p. 9153 - 9162
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Cleaner enzymatic production of biodiesel with easy separation procedures triggered by a biocompatible hydrophilic ionic liquid
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Green Chemistry p. 1944 - 1951
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Tert-butyl-end-capped polyynes: Crystallographic evidence of reduced bond length alternation
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Tert-butyl-end-capped polyynes: Crystallographic evidence of reduced bond length alternation
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Angewandte Chemie - International Edition p. 7915 - 7919
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Tert-butyl-end-capped polyynes: Crystallographic evidence of reduced bond length alternation
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Angewandte Chemie - International Edition p. 7915 - 7919
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Synthesis of 3-(5-amino-1: H -1,2,4-triazol-3-yl)propanamides and their tautomerism
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Template synthesis of [2]rotaxanes with large ring components and tris(biphenyl)methyl group as the blocking group. The relationship between the ring size and the stability of the rotaxanes
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Journal of Organic Chemistry p. 7477 - 7480
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Ruthenium-Catalyzed Cycloisomerization of 2,2′-Diethynyl- biphenyls Involving Cleavage of a Carbon-Carbon Triple Bond
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Chemistry - A European Journal p. 1941 - 1943
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Double Isomerization of Oxetane Amides to Azetidine Esters with Ring Expansion and Contraction
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Journal of Organic Chemistry p. 2253 - 2256
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Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists
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Bioorganic and Medicinal Chemistry Letters p. 3421 - 3424
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Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists
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Bioorganic and Medicinal Chemistry Letters p. 3421 - 3424
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LPAR1 Inhibitor. Medical application and preparation method thereof
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Using N-nitrosodichloroacetamides to conveniently convert linear primary amines into alcohols
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Synthetic Communications p. 2014 - 2021
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New Generation of Selective Androgen Receptor Degraders: Our Initial Design, Synthesis, and Biological Evaluation of New Compounds with Enzalutamide-Resistant Prostate Cancer Activity
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Journal of Medicinal Chemistry p. 491 - 511
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A convenient synthesis of 2,3,4,5-functionalised thieno[2,3-b]thiophenes
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Synthesis p. 735 - 741
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(E)-3-(2-(N-phenylcarbamoyl)vinyl)pyrrole-2-carboxylic acid derivatives. A novel class of glycine site antagonists
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Journal of Medicinal Chemistry p. 808 - 820
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Photocyclization Reactions. Part 7 [1]. Solvent and Substituent Effects in the Synthesis of Dihydrobenzofuranols Using Photocyclization of α-(2-Acylphenoxy)toluenes and Ethyl 2-Acylphenoxyacetates
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Journal of Heterocyclic Chemistry p. 1837 - 1849
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Novel 17-azolyl steroids, potent inhibitors of human cytochrome 17α- hydroxylase-C17,20-lyase (P450(17α)): Potential agents for the treatment of prostate cancer
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Journal of Medicinal Chemistry p. 902 - 912
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The reactivity of nitrophenyl substituted cyclic amines with dehydrogenations
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Zeitschrift fur Naturforschung, B: Chemical Sciences p. 37 - 48
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Heterocyclic compounds, which are inhibitors of the enzyme DPP-IV
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Alkine und Cumulene, XV. Ueber die Photodimerisierung konjugierter Enine
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Chemische Berichte p. 3772 - 3788
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Synthesis of ellipticine by hetaryne cycloadditions - Control of regioselectivity
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European Journal of Organic Chemistry p. 4543 - 4549
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Nickel-catalyzed decarbonylative polymerization of 5-alkynylphthalimides: A new methodology for the preparation of polyheterocycles
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Chemistry Letters p. 1566 - 1568
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Synthesis and central nervous system depressant activity of some bicyclic amides
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Journal of Medicinal Chemistry p. 436 - 438
(2007/10/06)
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- 20381-03-7
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Synthesis and central nervous system depressant activity of some bicyclic amides
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Journal of Medicinal Chemistry p. 436 - 438
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Novel spiroketal pyrrolidine GSK2336805 potently inhibits key hepatitis C virus genotype 1b mutants: From lead to clinical compound
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Journal of Medicinal Chemistry p. 2058 - 2073
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A selective fluorescent sensor for Zn2+ based on aggregation-induced emission (AIE) activity and metal chelating ability of bis(2-pyridyl)diphenylethylene
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Dalton Transactions p. 14039 - 14043
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Characterization of the anticonvulsant profile of valpromide derivatives
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Bioorganic and Medicinal Chemistry p. 3857 - 3869
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Design and synthesis of orally bioavailable inhibitors of inducible nitric oxide synthase. Synthesis and biological evaluation of dihydropyridin-2(1H)-imines and 1,5,6,7-tetrahydro-2H-azepin-2-imines
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Bioorganic and Medicinal Chemistry p. 689 - 702
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12-beta-Hydroxylation of bufalin and resibufogenin by Gibberella saubinetti
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Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 1092 - 1094
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