- 920018-72-0
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Total synthesis of phorboxazole A. 1. Preparation of four subunits
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Organic Letters p. 6039 - 6042
(2007/10/03)
- File number:4
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- 920025-46-3
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Process for making hydroisoindoline tachykinin receptor antagonists
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- File number:2
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- 920035-44-5
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The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations
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Bioorganic and Medicinal Chemistry Letters p. 2959 - 2966
(2008/12/23)
- File number:2
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- 920036-31-3
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Discovery of 3-{5-[(6-amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2- chlorophenoxy}-5-chlorobenzonitrile (MK-4965): A potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses
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Journal of Medicinal Chemistry p. 6503 - 6511
(2009/10/17)
- File number:2
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- 92009-88-6
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Design of Ligands containing the o-Hydroxybenzyl Group. Metal-complexing Properties of N,N''-Bis(2-hydroxybenzyl)diethylenetriamine-N,N',N''-triacetic Acid
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Journal of the Chemical Society, Dalton Transactions p. 2679 - 2686
(2007/10/02)
- File number:2
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- 92016-60-9
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Biomimetic synthesis and anti-inflammatory evaluation of violacin A analogues
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Bioorganic Chemistry
(2021/04/23)
- File number:2
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- 92016-66-5
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Functionalization of unprotected uracil derivatives using the halogen - Magnesium exchange
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Organic Letters p. 1639 - 1641
(2008/02/02)
- File number:2
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- 92016-70-1
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4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF
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- File number:2
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- 92020-24-1
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Rearrangement of allylic and propargylic alcohols catalyzed by the combined use of tetrabutylammonium perrhenate(VII) and p-toluenesulfonic acid
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Tetrahedron p. 2059 - 2068
(2007/10/02)
- File number:2
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- 92022-10-1
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Elaboration of the oxazepine ring system via cuI/L-proline-catalyzed intramolecular aryl amination
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Synlett p. 1833 - 1836
(2009/04/07)
- File number:3
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- 92022-83-8
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Modification of the clozapine structure by parallel synthesis
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Bioorganic and Medicinal Chemistry Letters p. 4548 - 4553
(2007/10/03)
- File number:2
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- 920268-18-4
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A smart magnetic resonance contrast agent for selective copper sensing
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Journal of the American Chemical Society p. 15942 - 15943
(2007/10/03)
- File number:2
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- 920270-28-6
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Design, synthesis, and structure-activity analysis of isoform-selective retinoic acid receptor β ligands
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Journal of Medicinal Chemistry p. 1540 - 1545
(2009/12/25)
- File number:2
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- 920285-05-8
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Novel 5-HT6 receptor antagonists/D2 receptor partial agonists targeting behavioral and psychological symptoms of dementia
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European Journal of Medicinal Chemistry p. 221 - 235
(2015/06/30)
- File number:2
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- 920285-21-8
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Fragment Based Optimization of Metabotropic Glutamate Receptor 2 (mGluR2) Positive Allosteric Modulators in the Absence of Structural Information
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Journal of Medicinal Chemistry p. 234 - 246
(2019/01/15)
- File number:3
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- 92029-41-9
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DIRECT PREPARATION OF 4-CARBOETHOXY-1,3-OXAZOLES
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Tetrahedron Letters p. 17 - 20
(2007/10/02)
- File number:8
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- 920301-52-6
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Discovery and biological evaluation of benzo[a]carbazole-based small molecule agonists of the thrombopoietin (Tpo) receptor
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Bioorganic and Medicinal Chemistry Letters p. 5255 - 5258
(2009/05/07)
- File number:2
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- 920314-24-5
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Preparation and conformational study of CF3-containing enkephalin-derived oligopeptide
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Tetrahedron p. 1888 - 1894
(2008/09/18)
- File number:2
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- 920318-17-8
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Synthesis of non-natural flavanones and dihydrochalcones in metabolically engineered yeast
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Journal of Molecular Catalysis B: Enzymatic p. 257 - 263
(2010/11/18)
- File number:2
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- 92033-74-4
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Structural optimization of azadipeptide nitriles strongly increases association rates and allows the development of selective cathepsin inhibitors
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Journal of Medicinal Chemistry p. 396 - 400
(2011/03/18)
- File number:4
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- 92034-59-8
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Sulfide derivatives of cysteine. II. Some sulfonamide derivatives of cysteine and methionine.
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Journal of Pharmaceutical Sciences p. 576 - 579
(2007/10/09)
- File number:4
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- 92038-37-4
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One-pot ozonolytic synthesis of acyclic α,ω-bifunctional compounds from methyl 10-undecenoate and 10-undecen-1-ol
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Russian Journal of Applied Chemistry p. 935 - 940
(2015/10/12)
- File number:2
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- 92040-10-3
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α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter: A pharmacological characterization of interactions between pyrrolidinopropiophenones and uptake1 and uptake2 monoamine transporters
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Neuropharmacology
(2021/05/04)
- File number:2
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- 920491-98-1
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Heck reactions of quinoline-derived nonaflates
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Synlett p. 2993 - 2996
(2008/03/11)
- File number:2
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- 920509-39-3
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Discovery of 2-[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydropyridazin-3- yloxy)phenyl]-3,5-dioxo-2,3,4,5-tetrahydro[1,2,4]triazine-6-carbonitrile (MGL-3196), a highly selective thyroid hormone receptor β agonist in clinical trials for the treatment of dyslipidemia
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Journal of Medicinal Chemistry p. 3912 - 3923
(2014/06/09)
- File number:2
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- 920509-81-5
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THYROID HORMONE RECEPTOR AGONISTS
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- File number:2
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- 920510-95-8
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PIPERAZINE HETEROARYL DERIVATES AS GPR38 AGONISTS
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- File number:2
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- 920514-00-7
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Efficient synthesis of medium-sized rings incorporating indole or pyrrole units by samarium diiodide induced cyclizations
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European Journal of Organic Chemistry p. 4989 - 4992
(2007/10/03)
- File number:2
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- 920525-59-3
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Structure based optimization of chromen-based TNF-α converting enzyme (TACE) inhibitors on S1′ pocket and their quantitative structure-activity relationship (QSAR) study
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Bioorganic and Medicinal Chemistry p. 8618 - 8629
(2011/02/25)
- File number:2
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- 920525-60-6
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NOVEL CHROMEN-2-ONE BASED HYDROXAMIC ACID DERIVATIVES HAVING ANTI-INFLAMMATORY ACTIVITY, THE PREPARATION THEREOF AND A COMPOSITION CONTAINING THE SAME FOR TREATING INFLAMMATORY DISEASE
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- File number:2
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- 92061-22-8
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Synthesis and antimicrobial activity of novel 1,3,4-oxadiazolyl-quinazolin- 4(3H)ones
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Journal of Heterocyclic Chemistry p. 923 - 931
(2010/11/04)
- File number:2
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- 92071-84-6
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Characterization of air/water interface adsorption of a series of partially fluorinated/hydrogenated quaternary ammonium salts
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Journal of Fluorine Chemistry p. 241 - 248
(2015/09/02)
- File number:2
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- 920739-78-2
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Compounds and their salts specific to the PPAR receptors and the EGF receptors and their use in the medical field
-
- File number:2
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- 92074-28-7
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Iron-Catalyzed Regiodivergent Hydrostannation of Alkynes: Intermediacy of Fe(IV)-H versus Fe(II)-Vinylidene
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Journal of the American Chemical Society p. 409 - 419
(2021/01/12)
- File number:8
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- 920744-20-3
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New strategy for the synthesis of phosphatase inhibitors TMC-69-6H and analogs
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Tetrahedron Letters p. 9305 - 9308
(2007/10/03)
- File number:2
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- 920749-72-0
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Cleavage of a chiral auxiliary using RCM on an especially sterically crowded alkene: Syntheses of chiral carbo- and heterocycles
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Journal of Organometallic Chemistry p. 5336 - 5355
(2007/10/03)
- File number:2
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- 920749-74-2
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Cleavage of a chiral auxiliary using RCM on an especially sterically crowded alkene: Syntheses of chiral carbo- and heterocycles
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Journal of Organometallic Chemistry p. 5336 - 5355
(2007/10/03)
- File number:2
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- 920750-06-7
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Efficient preparation of chiral non-racemic sulfur compounds
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Canadian Journal of Chemistry p. 603 - 618
(2008/02/12)
- File number:2
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- 920754-85-4
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1,2,3,4-Tetraethynylbenzene as a template for cobalt-catalyzed alkyne cocyclizations: Synthesis of 2,3,8,9-tetrakis(trimethylsilyl) angular [3]phenylene and bent [5]phenylene (benzo[1″,2″:3,4;3″, 4″:3′,4′]dicyclobuta[1,2-b:1′,2′-b′] bisbiphenylene)
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Synlett p. 2981 - 2984
(2008/03/11)
- File number:2
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- 920757-34-2
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A facile and efficient synthesis of d3-labelled Reyataz
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Journal of labelled compounds and radiopharmaceuticals p. 1041 - 1047
(2007/10/03)
- File number:2
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- 920757-94-4
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Ring-closing metathesis in the synthesis of BC ring-systems of taxol
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Chemistry - A European Journal p. 7314 - 7323
(2009/08/07)
- File number:2
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- 920758-02-7
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Synthesis of model BC bicycles of taxol using C10-C11 ring-closing metathesis strategy
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Journal of Organometallic Chemistry p. 5438 - 5443
(2007/10/03)
- File number:2
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- 920796-72-1
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Scandium(III) triflate mediated intramolecular ring expansion of aziridines: A direct access to 4-aryltetrahydroisoquinolines
-
Tetrahedron Letters p. 6787 - 6790
(2015/01/08)
- File number:2
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- 920796-73-2
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2-(2-Phenylmorpholin-4-yl)pyrimidin-4(3H)-ones; A new class of potent, selective and orally active glycogen synthase kinase-3β inhibitors
-
Bioorganic and Medicinal Chemistry Letters p. 6933 - 6937
(2014/01/06)
- File number:3
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- 920797-21-3
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2-(2-Phenylmorpholin-4-yl)pyrimidin-4(3H)-ones; A new class of potent, selective and orally active glycogen synthase kinase-3β inhibitors
-
Bioorganic and Medicinal Chemistry Letters p. 6933 - 6937
(2014/01/06)
- File number:3
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- 92082-85-4
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Synthesis and molecular modelling studies of novel sulphonamide derivatives as dengue virus 2 protease inhibitors
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Bioorganic Chemistry p. 74 - 82
(2015/08/11)
- File number:2
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- 92089-09-3
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Facile Conversion of Hantzsch Type 4-Aryl-2,6-dimethyl-1,4-dihydropyridine-3,5-carboxylates into 4-Aryl-2-methyl-5-oxo-1,4,5,7-tetrahydrofuropyridine-3-carboxylates
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Synthesis p. 617 - 618
(2007/10/02)
- File number:5
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- 920986-09-0
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The Heck reaction of β-arylacrylamides: An approach to 4-aryl-2-quinolones
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Synlett p. 2947 - 2952
(2008/02/12)
- File number:2
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- 92102-83-5
-
CARBOXYLIC ACID ARYL AMIDES
-
- File number:2
-
- 92103-22-5
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Repurposing Hsp90 inhibitors as antibiotics targeting histidine kinases
-
Bioorganic and Medicinal Chemistry Letters p. 5235 - 5244
(2017/11/01)
- File number:2
-