- 104680-25-3
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Therapeutically Active Fused Pyrimidine Derivatives
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- File number:3
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- 104680-44-6
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An Examination of O-2-Isocephems as Orally Absorbable Antibiotics
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Journal of Medicinal Chemistry p. 1190 - 1196
(2007/10/02)
- File number:5
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- 104681-15-4
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v-Triazolines. Part 25. 4,5-Dihydro-4-methylene-5-morpholino-1-(4-substituted-phenyl)-v-triazoles: an n.m.r. study.
-
Journal of Chemical Research, Miniprint p. 1233 - 1252
(2007/10/02)
- File number:1
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- 1046811-99-7
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Iridium-catalyzed vinylic C-H borylation of cyclic vinyl ethers by bis(pinacolato)diboron
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Chemistry Letters p. 664 - 665
(2008/12/21)
- File number:3
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- 1046812-02-5
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Metal-catalyzed reactions of organoboronic acids and esters
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Bulletin of the Chemical Society of Japan p. 1535 - 1553
(2009/05/06)
- File number:2
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- 1046812-03-6
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Iridium-catalyzed vinylic C-H borylation of cyclic vinyl ethers by bis(pinacolato)diboron
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Chemistry Letters p. 664 - 665
(2008/12/21)
- File number:2
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- 104681-55-2
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Sulfoxide induced sigmatropic rearrangement (SISR) of methyl 1-methylsulfanylvinyl sulfoxides
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Chemical Communications p. 1011 - 1012
(2007/10/03)
- File number:2
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- 1046815-82-0
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Synthesis and SAR studies of bicyclic amine series GPR119 agonists
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Bioorganic and Medicinal Chemistry Letters p. 5123 - 5128
(2012/08/28)
- File number:5
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- 1046816-12-9
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A Series of Analogues to the AT2R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding Mode
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ChemistryOpen p. 114 - 125
(2019/02/07)
- File number:2
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- 10468-16-3
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Regioselective installation of fluorosulfate (-OSO2F) functionality into aromatic C(sp2)-H bonds for the construction of: Para-amino-arylfluorosulfates
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Chemical Communications p. 6273 - 6276
(2019/06/07)
- File number:32
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- 1046816-38-9
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PYRAZOLE DERIVATIVES AS DIHYDROOROTATE DEHYDROGENASE (DHODH) INHIBITORS
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- File number:2
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- 1046816-40-3
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HETEROCYCLIC COMPOUND AS CSF-1R INHIBITOR AND USE THEREOF
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- File number:2
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- 1046816-75-4
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CYCLOAMINO DERIVATIVES AS GPR119 ANTAGONISTS
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- File number:3
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- 1046817-01-9
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COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY
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- File number:4
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- 1046817-22-4
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Discovery of Quinoxaline-Based P1-P3 Macrocyclic NS3/4A Protease Inhibitors with Potent Activity against Drug-Resistant Hepatitis C Virus Variants
-
Journal of Medicinal Chemistry p. 11972 - 11989
(2021/09/06)
- File number:11
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- 10468-17-4
-
Regioselective installation of fluorosulfate (-OSO2F) functionality into aromatic C(sp2)-H bonds for the construction of: Para-amino-arylfluorosulfates
-
Chemical Communications p. 6273 - 6276
(2019/06/07)
- File number:25
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- 104681-82-5
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Alcoxymethyltributyletains precurseurs d'alcoxymethyllithiums: application a la synthese de monoethers d'α-glycols et a l'homologation de cetones en aldehydes
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Bulletin de la Societe Chimique de France p. 787 - 793
(2007/10/02)
- File number:2
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- 1046818-33-0
-
NITROGEN CONTAINING HETEROCYCLIC COMPOUNDS USEFUL AS BIFUNCTIONAL MODULATORS OF M3 RECEPTORS AND BETA-2 RECEPTORS
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- File number:1
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- 104681-89-2
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α-Hydroxylation of carbonyls using iodine
-
Tetrahedron Letters p. 447 - 450
(2007/10/03)
- File number:3
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- 104681-90-5
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Ozonolysis of Vinyl Ethers. Evidence for Intramolecular Oxygen Transfer from a Carbonyl Oxide Moiety to a Methoxyvinyl Group
-
Journal of the American Chemical Society p. 4969 - 4973
(2007/10/02)
- File number:4
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- 104681-92-7
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Design, synthesis, and structure-activity relationship of novel CCR2 antagonists
-
Bioorganic and Medicinal Chemistry Letters p. 1830 - 1834
(2009/11/30)
- File number:26
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- 104682-02-2
-
Amino acid derivatives having anti-tumor activity and compositions containing them
-
- File number:1
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- 10468-24-3
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Asymmetrie copper-catalyzed propargylic substitution reaction of propargylic acetates with enamines
-
Organic Letters p. 4612 - 4615
(2009/12/09)
- File number:7
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- 10468-25-4
-
Reactions of silylcarbamates with ketones
-
Tetrahedron Letters p. 8937 - 8939
(2007/10/03)
- File number:4
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- 10468-26-5
-
Enamines: efficient nucleophiles for the palladium-catalyzed asymmetric allylic alkylation
-
Tetrahedron p. 512 - 517
(2009/04/07)
- File number:12
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- 104682-97-5
-
C7-Indole Amidations and Alkenylations by Ruthenium(II) Catalysis
-
Angewandte Chemie - International Edition p. 12534 - 12540
(2020/07/06)
- File number:11
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- 10468-30-1
-
Cation Exchange Induced Transformation of InP Magic-Sized Clusters
-
Chemistry of Materials p. 7984 - 7992
(2017/10/03)
- File number:32
-
- 104683-03-6
-
THALLIUM IN ORGANIC SYNTHESIS. 68. A CONVENIENT SYNTHESIS OF 2-PHENYLINDOLES FROM ANILIDES
-
Tetrahedron Letters p. 5963 - 5966
(2007/10/02)
- File number:1
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- 104683-04-7
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Multicatalytic one-pot reaction of 1-(2-alkynylphenyl)ketoximes for generation of indole derivatives
-
Organic Letters p. 3975 - 3977
(2010/11/04)
- File number:6
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- 104683-07-0
-
HIGHLY STEREOSELECTIVE SYNTHESIS OF (2E,4E)-DIENAMIDES AND (2E,4E)-DIENOATES VIA A DOUBLE ELIMINATION REACTION
-
Tetrahedron Letters p. 603 - 606
(2007/10/02)
- File number:1
-
- 104683-09-2
-
HIGHLY STEREOSELECTIVE SYNTHESIS OF (2E,4E)-DIENAMIDES AND (2E,4E)-DIENOATES VIA A DOUBLE ELIMINATION REACTION
-
Tetrahedron Letters p. 603 - 606
(2007/10/02)
- File number:1
-
- 104683-10-5
-
HIGHLY STEREOSELECTIVE SYNTHESIS OF (2E,4E)-DIENAMIDES AND (2E,4E)-DIENOATES VIA A DOUBLE ELIMINATION REACTION
-
Tetrahedron Letters p. 603 - 606
(2007/10/02)
- File number:1
-
- 104683-11-6
-
HIGHLY STEREOSELECTIVE SYNTHESIS OF (2E,4E)-DIENAMIDES AND (2E,4E)-DIENOATES VIA A DOUBLE ELIMINATION REACTION
-
Tetrahedron Letters p. 603 - 606
(2007/10/02)
- File number:1
-
- 1046831-94-0
-
Discovery of Potent and Selective 7-Azaindole Isoindolinone-Based PI3KγInhibitors
-
ACS Medicinal Chemistry Letters p. 2244 - 2252
(2020/12/17)
- File number:10
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- 1046831-98-4
-
Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway
-
Angewandte Chemie - International Edition p. 1062 - 1066
(2019/01/04)
- File number:4
-
- 1046832-00-1
-
Red phosphorescence compounds and organic light-emitting device applying the compounds
-
- File number:8
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- 1046832-21-6
-
SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE
-
- File number:7
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- 10468-32-3
-
Regioselective silver-mediated Kondakov-Darzens olefin acylation
-
Chemistry - A European Journal p. 12912 - 12916
(2011/12/04)
- File number:5
-
- 10468-36-7
-
Cyclobutyl phenyl sulfoxide and (SR)-cyclobutyl p-tolyl sulfoxide: New reagents for the spiroannelation of cyclopentanone
-
Tetrahedron Letters p. 4985 - 4988
(2007/10/02)
- File number:10
-
- 10468-37-8
-
Intramolecular Sulfur Ylide Additions to Ketones
-
Journal of Organic Chemistry p. 5372 - 5380
(2007/10/02)
- File number:2
-
- 10468-40-3
-
A Solvent-Free Process for Synthesis of Imines by Iron-Catalyzed Oxidative Self- or Cross-Condensation of Primary Amines Using Molecular Oxygen as Sole Oxidant
-
Catalysis Letters p. 1648 - 1654
(2016/08/30)
- File number:73
-
- 10468-46-9
-
Selective conversion of nitroarenes using a carbon nanotube-ruthenium nanohybrid
-
Chemical Communications p. 1739 - 1742
(2015/03/03)
- File number:8
-
- 104684-74-4
-
A CONVENIENT AND GENERAL APPROACH TO THE SYNTHESIS OF PROPERLY PROTECTED d-NUCLEOSIDE-3'-HYDROGENPHOSPHONATES VIA PHOSPHITE INTERMEDIATES
-
Tetrahedron Letters p. 2661 - 2664
(2007/10/02)
- File number:3
-
- 104685-75-8
-
Novel indanyl-substituted imidazo[1,2-a]pyridines as potent reversible inhibitors of the gastric H+/K+-ATPase
-
Bioorganic and Medicinal Chemistry Letters p. 5374 - 5378
(2008/09/21)
- File number:6
-
- 104685-76-9
-
Novel indanyl-substituted imidazo[1,2-a]pyridines as potent reversible inhibitors of the gastric H+/K+-ATPase
-
Bioorganic and Medicinal Chemistry Letters p. 5374 - 5378
(2008/09/21)
- File number:11
-
- 1046859-34-0
-
Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1h- pyrazol-1-yl)ethoxy]-6-methylphenyl}-n-(2,2-difluoropropyl)-5, 7-dihydro-6h-pyrrolo[3,4-d]pyrimidine-6-carboxamide
-
Journal of Medicinal Chemistry p. 3368 - 3385
(2011/06/27)
- File number:1
-
- 1046861-17-9
-
Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1h- pyrazol-1-yl)ethoxy]-6-methylphenyl}-n-(2,2-difluoropropyl)-5, 7-dihydro-6h-pyrrolo[3,4-d]pyrimidine-6-carboxamide
-
Journal of Medicinal Chemistry p. 3368 - 3385
(2011/06/27)
- File number:3
-
- 1046861-47-5
-
Development of a Scalable Enantioselective Synthesis of JAK Inhibitor Upadacitinib
-
Organic Process Research and Development p. 949 - 962
(2021/10/21)
- File number:6
-
- 1046861-62-4
-
4-PHENYLPYRANE-3,5-DIONES, 4-PHENYLTHIOPYRANE-3,5-DIONES AND 2-PHENYLCYCLOHEXANE-1,3,5-TRIONES AS HERBICIDES
-
- File number:2
-
- 10468-61-8
-
Design, synthesis, structure, and dehydrogenation reactivity of a water soluble o-iodoxybenzoic acid derivative bearing a trimethylammonium group
-
Organic Letters p. 6488 - 6491
(2012/02/02)
- File number:7
-
