- 103517-81-3
-
An Efficient Synthesis of Dialkyl 2-Oxoalkanephosphonates and Diphenyl-2-oxoalkylphosphine Oxides from 1-Chloralkyl Ketones
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Synthesis p. 1048 - 1051
(2007/10/02)
- File number:2
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- 10351-88-9
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Oxidative aryl-aryl, aryl-benzyl coupling of lignans-reactions of phyllanthin and haloderivatives with TTFA, DDQ, Li/THF)))): Synthesis of dibenzocyclooctadiene system and phyltetralin
-
Tetrahedron p. 8277 - 8284
(2007/10/02)
- File number:3
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- 1035-19-4
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Tetrahydrofolate Coenzyme Models: Synthesis of Tetrahydroimidazoisoquinolines and Tetrahydroimidazoquinolines
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Journal of the Chemical Society. Perkin transactions I p. 385 - 391
(2007/10/02)
- File number:3
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- 103519-90-0
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Pd-Catalyzed α-Selective C-H Functionalization of Olefins: En Route to 4-Imino-β-Lactams
-
Journal of the American Chemical Society p. 2146 - 2149
(2016/03/05)
- File number:10
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- 1035202-87-9
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Lewis base activation of Lewis acids: Catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes
-
Journal of Organic Chemistry p. 4582 - 4595
(2008/09/21)
- File number:2
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- 1035204-90-0
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NOVEL PROCESS FOR THE SYNTHESIS OF [R-(R*, R*)]-2-(4-FLUOROPHENYL)-BETA, DELTA-DIHYDROXY-5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)CARBONYL]-1H-PYRROLE-1-HEPTANOIC ACID OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
-
- File number:1
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- 103521-31-9
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Quantitative determination of forphenicinol and its metabolites in human serum and urine by gas chromatography/mass spectrometry with selected ion monitoring
-
Chemical and Pharmaceutical Bulletin p. 3290 - 3297
(2007/10/02)
- File number:1
-
- 10352-14-4
-
Reactions of π-deficient aromatic heterocycles with ammonium polyhalides. I. Halogenation of acridone and acridine derivatives using benzyltriethylammonium (BTEA) polyhalides
-
Synthetic Communications p. 3493 - 3501
(2007/10/03)
- File number:7
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- 103521-70-6
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Synthesis and biological activity of two new calcium-channel blockers, mebudipine and dibudipine
-
Journal of Pharmacy and Pharmacology p. 1229 - 1233
(2007/10/03)
- File number:2
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- 1035217-25-4
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A novel rearrangement reaction conversion of 3-(chloromethyl)azetidin-2-ones to azetidine-3-carboxylic acid esters
-
Tetrahedron Letters p. 4795 - 4798
(2007/10/02)
- File number:1
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- 1035218-87-1
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5- [4- (AZETIDIN-3-YL0XY) -PHENYL] -2-PHENYL-5H-THIAZ0L0 [5,4-C] PYRIDIN-4-0NE DERIVATIVES AND THEIR USE AS MCH RECEPTOR ANTAGONISTS
-
- File number:1
-
- 1035219-80-7
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5- [4- (AZETIDIN-3-YL0XY) -PHENYL] -2-PHENYL-5H-THIAZ0L0 [5,4-C] PYRIDIN-4-0NE DERIVATIVES AND THEIR USE AS MCH RECEPTOR ANTAGONISTS
-
- File number:2
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- 1035219-96-5
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Dihydrothiazolopyridone derivatives as a novel family of positive allosteric modulators of the metabotropic glutamate 5 (mGlu5) receptor
-
Journal of Medicinal Chemistry p. 7243 - 7259
(2013/10/21)
- File number:6
-
- 103522-32-3
-
MAGNESIUM-METHANOL AS A SIMPLE CONVENIENT REDUCING AGENT FOR Α,Β-UNSATURATED ESTERS
-
Tetrahedron Letters p. 2409 - 2410
(2007/10/02)
- File number:2
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- 103522-34-5
-
Novel atropisomeric bisphosphine ligands with a bridge across the 5,5′-position of the biphenyl for asymmetric catalysis
-
Tetrahedron Asymmetry p. 482 - 488
(2008/09/19)
- File number:9
-
- 1035224-56-6
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SUBSTITUTE 1, 6-NAPHTHYRIDINES FOR USE AS SCD INHIBITORS
-
- File number:2
-
- 1035225-98-9
-
Efficient synthesis of 2-mono and 2,3-disubstituted indoles via palladium-catalyzed oxidation of aminoalcohols
-
Heterocycles p. 1055 - 1059
(2008/12/20)
- File number:1
-
- 1035225-99-0
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Efficient synthesis of 2-mono and 2,3-disubstituted indoles via palladium-catalyzed oxidation of aminoalcohols
-
Heterocycles p. 1055 - 1059
(2008/12/20)
- File number:1
-
- 10352-28-0
-
Mild Access to N-Formylation of Primary Amines using Ethers as C1 Synthons under Metal-Free Conditions
-
Advanced Synthesis and Catalysis p. 3960 - 3968
(2018/09/10)
- File number:17
-
- 1035229-31-2
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:4
-
- 1035229-32-3
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:6
-
- 1035229-33-4
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:6
-
- 1035229-34-5
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:5
-
- 1035229-41-4
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:3
-
- 1035229-42-5
-
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
-
ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:2
-
- 1035230-24-0
-
Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-chloro- N 2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)- N 4-(2-(isopropylsulfonyl) phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials
-
Journal of Medicinal Chemistry p. 5675 - 5690
(2013/08/23)
- File number:10
-
- 10352-30-4
-
4-Phenyl-2-(1-piperazinyl)quinolines with potent antidepressant activity
-
Chemical and Pharmaceutical Bulletin p. 2618 - 2622
(2007/10/02)
- File number:4
-
- 10352-33-7
-
Reactions of π-deficient aromatic heterocycles with ammonium polyhalides. I. Halogenation of acridone and acridine derivatives using benzyltriethylammonium (BTEA) polyhalides
-
Synthetic Communications p. 3493 - 3501
(2007/10/03)
- File number:3
-
- 1035235-03-0
-
A facile synthetic route for 2-pyridyl derivatives: direct preparation of a stable 2-pyridylzinc bromide and its copper-free and pd-catalyzed coupling reactions
-
Tetrahedron Letters p. 5329 - 5331
(2009/12/06)
- File number:4
-
- 1035235-10-9
-
Discovery of Highly Potent Inhibitors Targeting the Predominant Drug-Resistant S31N Mutant of the Influenza A Virus M2 Proton Channel
-
Journal of Medicinal Chemistry p. 1207 - 1216
(2016/02/23)
- File number:2
-
- 103523-52-0
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:2
-
- 1035235-26-7
-
HETEROCYCLE SUBSTITUTED AMINO-PYRIDINE COMPOUNDS AND METHODS OF USE THEREOF
-
- File number:6
-
- 1035235-27-8
-
Phase Separation Macrocyclization in a Complex Pharmaceutical Setting: Application toward the Synthesis of Vaniprevir
-
Journal of Organic Chemistry p. 7576 - 7582
(2017/07/26)
- File number:11
-
- 1035235-29-0
-
HETEROCYCLIC COMPOUND AND USE THEREOF
-
- File number:7
-
- 103524-39-6
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 10352-44-0
-
Sulfuryl Fluoride Mediated Synthesis of Amides and Amidines from Ketoximes via Beckmann Rearrangement
-
Chemistry - A European Journal p. 10402 - 10405
(2020/07/25)
- File number:7
-
- 103524-46-5
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103524-49-8
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103524-52-3
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103524-55-6
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103524-82-9
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103524-92-1
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103525-06-0
-
Novel phenoxyalkylamine derivatives. II. Synthesis and Ca2+-antagonistic activities of α-alkyl-α-[(phenoxypropylamino)propyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 373 - 385
(2007/10/02)
- File number:1
-
- 103525-11-7
-
Novel phenoxyalkylamine derivatives. I. Synthesis and pharmacological activities of α-isopropyl-α-[(phenoxyalkylamino)alkyl]-benzeneacetonitrile derivatives
-
Chemical and Pharmaceutical Bulletin p. 367 - 372
(2007/10/02)
- File number:1
-
- 103-52-6
-
Synthesis of aromatic alcohols and their alkanoic acid esters
-
Russian Journal of Applied Chemistry p. 408 - 410
(2008/02/03)
- File number:12
-
- 10352-60-0
-
Structure-activity relationship of quinoline derivatives as potent and selective α2c-adrenoceptor antagonists
-
Journal of Medicinal Chemistry p. 6351 - 6363
(2007/10/03)
- File number:6
-
- 1035260-90-2
-
NAPHTHALENONE COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:1
-
- 1035260-93-5
-
NAPHTHALENONE COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:1
-
