- 105399-96-0
-
A Simple and Convenient Method for the Preparation of N,N'-Dibenzyldiaza-crown Compounds
-
Journal of Organic Chemistry p. 1808 - 1810
(2007/10/02)
- File number:2
-

- 105400-04-2
-
Syntheses and Binding Properties of Bibracchial Lariat Ethers (BIBLEs): Survey of Synthetic Methods and Cation Selectivities
-
Journal of Organic Chemistry p. 5373 - 5384
(2007/10/02)
- File number:4
-

- 105400-15-5
-
Syntheses and Binding Properties of Bibracchial Lariat Ethers (BIBLEs): Survey of Synthetic Methods and Cation Selectivities
-
Journal of Organic Chemistry p. 5373 - 5384
(2007/10/02)
- File number:3
-

- 105400-16-6
-
Syntheses of unsymmetrically N,N′-bis (substituted)-4,13-diaza-18-crown-6-ether derivatives as a new electron donor-spacer-acceptor triad
-
Tetrahedron Letters p. 95 - 98
(2007/10/02)
- File number:3
-

- 105400-43-9
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Tailored α-methylene-γ-butyrolactones and their effects on growth suppression in pancreatic carcinoma cells
-
Bioorganic and Medicinal Chemistry Letters p. 6620 - 6623
(2010/12/19)
- File number:9
-

- 105400-81-5
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Syntheses of cisoid and transoid analogs of phenethylamine.
-
Journal of Medicinal Chemistry p. 109,112
(2007/10/04)
- File number:6
-

- 105401-16-9
-
Molecular modification of anticholinergics as probes for probes for muscarinic receptors. 3. Conformationally restricted analogues of benactyzine
-
Journal of Medicinal Chemistry p. 278 - 285
(2007/10/02)
- File number:1
-

- 105401-17-0
-
Molecular modification of anticholinergics as probes for probes for muscarinic receptors. 3. Conformationally restricted analogues of benactyzine
-
Journal of Medicinal Chemistry p. 278 - 285
(2007/10/02)
- File number:2
-

- 105401-18-1
-
Molecular modification of anticholinergics as probes for probes for muscarinic receptors. 3. Conformationally restricted analogues of benactyzine
-
Journal of Medicinal Chemistry p. 278 - 285
(2007/10/02)
- File number:2
-

- 105401-20-5
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Molecular modification of anticholinergics as probes for probes for muscarinic receptors. 3. Conformationally restricted analogues of benactyzine
-
Journal of Medicinal Chemistry p. 278 - 285
(2007/10/02)
- File number:2
-

- 105401-49-8
-
Gemfibrozil derivatives as activators of soluble guanylyl cyclase – A structure-activity study
-
European Journal of Medicinal Chemistry
(2021/08/09)
- File number:2
-

- 105401-52-3
-
Chemoenzymatic Preparation of Enantiomerically Enriched (R)-(–)-Mandelic Acid Derivatives: Application in the Synthesis of the Active Agent Pemoline
-
European Journal of Organic Chemistry p. 2290 - 2304
(2017/05/01)
- File number:4
-

- 105401-59-0
-
Arylpyran Pseudoacid Racemization: Rate Estimation and Structural Influences
-
Journal of Chemical Crystallography p. 14 - 41
(2020/04/29)
- File number:6
-

- 105401-60-3
-
Ligand-Controlled Regiodivergence in Nickel-Catalyzed Hydroarylation and Hydroalkenylation of Alkenyl Carboxylic Acids**
-
Angewandte Chemie - International Edition p. 23306 - 23312
(2020/10/19)
- File number:3
-

- 105401-62-5
-
Highly Active Manganese-Mediated Acylation of Alcohols with Acid Chlorides or Anhydrides
-
Synlett p. 2665 - 2669
(2017/10/07)
- File number:3
-

- 105401-68-1
-
Stereochemical considerations and the antiinflammatory activity of 6-amino-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ols and related derivatives
-
Journal of Medicinal Chemistry p. 20 - 27
(2007/10/02)
- File number:3
-

- 105401-73-8
-
A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid
-
Bulletin of the Chemical Society of Japan p. 1516 - 1527
(2007/10/02)
- File number:4
-

- 105402-24-2
-
BENZIMIDAZOLYL-PYRIDINE COMPOUNDS FOR INFLAMMATION AND IMMUNE-RELATED USES
-
- File number:3
-

- 10540-29-1
-
Nickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes
-
Journal of the American Chemical Society p. 3189 - 3192
(2015/03/30)
- File number:69
-

- 10540-31-5
-
Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of potassium aryl- and heteroaryltrifluoroborates
-
Journal of Organic Chemistry p. 4302 - 4314
(2007/10/03)
- File number:46
-

- 10540-32-6
-
Biaryl and aryl ketone synthesis via Pd-catalyzed decarboxylase coupling of carboxylate salts with aryl triflates
-
Chemistry - A European Journal p. 9336 - 9349
(2010/04/03)
- File number:18
-

- 10540-33-7
-
Phase-Transfer-Catalyzed Gomberg-Bachmann Synthesis of Unsymmetrical Biarenes: A Survey of Catalysts and Substrates
-
Journal of Organic Chemistry p. 1594 - 1603
(2007/10/02)
- File number:1
-

- 10540-35-9
-
Phase-Transfer-Catalyzed Gomberg-Bachmann Synthesis of Unsymmetrical Biarenes: A Survey of Catalysts and Substrates
-
Journal of Organic Chemistry p. 1594 - 1603
(2007/10/02)
- File number:2
-

- 10540-36-0
-
Efficient cobalt-catalyzed formation of unsymmetrical biaryl compounds and its application in the synthesis of a sartan intermediate
-
Angewandte Chemie - International Edition p. 2089 - 2092
(2009/02/06)
- File number:2
-

- 10540-39-3
-
A focused fragment library targeting the antibiotic resistance enzyme - Oxacillinase-48: Synthesis, structural evaluation and inhibitor design
-
European Journal of Medicinal Chemistry p. 634 - 648
(2018/01/19)
- File number:9
-

- 10540-41-7
-
F-NMR-spectroscopy for the identification of photo products generated from aromatic iodo compounds - IV
-
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy p. 689 - 692
(2007/10/02)
- File number:2
-

- 105404-33-9
-
Deoxygenation Reactions of ortho-Nitrostyrenes with Carbon Monoxide Catalysed by Metal Carbonyls: a New Route to Indoles
-
Journal of the Chemical Society. Chemical communications p. 784 - 786
(2007/10/02)
- File number:1
-

- 10540-43-9
-
Activation of Reducing Agents. Sodium Hydride Containing Complex Reducing Agents. 32. NiCRAL's as Very Efficient Agents in Promoting Cross-Coupling of Aryl Halides
-
Journal of Organic Chemistry p. 4844 - 4848
(2007/10/02)
- File number:1
-

- 10540-45-1
-
Palladium-catalyzed dehydrative aromatization of cyclohexenone oximes to anilines
-
Synthetic Communications p. 1441 - 1446
(2007/10/02)
- File number:13
-

- 105404-65-7
-
A natural product inspired fragment-based approach towards the development of novel anti-bacterial agents
-
MedChemComm p. 1387 - 1391
(2016/07/21)
- File number:16
-

- 105404-89-5
-
Intramolecular cascade hydroarylation/cycloisomerization strategy for the synthesis of polycyclic aromatic and heteroaromatic systems
-
European Journal of Organic Chemistry p. 260 - 263
(2013/02/25)
- File number:7
-

- 105404-90-8
-
A GENERAL PROCEDURE FOR THE SYNTHESIS OF METHYLTHIO-, METHYLSELENO- AND METHYLTELLURO-SUBSTITUTED AROMATIC COMPOUNDS
-
Journal of Organometallic Chemistry p. 357 - 366
(2007/10/02)
- File number:5
-

- 105404-91-9
-
Cyanines as new fluorescent probes for DNA detection and two-photon excited bioimaging
-
Organic Letters p. 2194 - 2197
(2010/08/07)
- File number:6
-

- 105405-07-0
-
Synthesis and antihypertensive activity of 5-(2-hydroxyphenyl)-1-(3-mercaptopropionyl)-2-pyrrolidinecarboxylic acids
-
Chemical and Pharmaceutical Bulletin p. 4836 - 4846
(2007/10/02)
- File number:1
-

- 105405-11-6
-
Synthesis and antihypertensive activity of 5-(2-hydroxyphenyl)-1-(3-mercaptopropionyl)-2-pyrrolidinecarboxylic acids
-
Chemical and Pharmaceutical Bulletin p. 4836 - 4846
(2007/10/02)
- File number:1
-

- 105405-12-7
-
Synthesis and antihypertensive activity of 5-(2-hydroxyphenyl)-1-(3-mercaptopropionyl)-2-pyrrolidinecarboxylic acids
-
Chemical and Pharmaceutical Bulletin p. 4836 - 4846
(2007/10/02)
- File number:1
-

- 105405-14-9
-
Synthesis and antihypertensive activity of 5-(2-hydroxyphenyl)-1-(3-mercaptopropionyl)-2-pyrrolidinecarboxylic acids
-
Chemical and Pharmaceutical Bulletin p. 4836 - 4846
(2007/10/02)
- File number:1
-

- 105405-15-0
-
Synthesis and antihypertensive activity of 5-(2-hydroxyphenyl)-1-(3-mercaptopropionyl)-2-pyrrolidinecarboxylic acids
-
Chemical and Pharmaceutical Bulletin p. 4836 - 4846
(2007/10/02)
- File number:1
-

- 105405-22-9
-
Design and synthesis of antitumor compounds based on the cytotoxic diterpenoids from the genus Rabdosia
-
Chemical and Pharmaceutical Bulletin p. 685 - 689
(2007/10/02)
- File number:7
-

- 105-40-8
-
1,3 Dimethyl 3 acyltriazenes: Synthesis and chemistry of a novel class of biological methylating agents
-
Journal of Organic Chemistry p. 3751 - 3757
(2007/10/02)
- File number:40
-

- 105408-01-3
-
A new class of HIV-1-specific 6-substituted acyclouridine derivatives: Synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)
-
Journal of Medicinal Chemistry p. 349 - 357
(2007/10/02)
- File number:1
-

- 105408-69-3
-
The synthesis and antilipidperoxidation activity of 4,4-diarylbutylamines and 4,4-diarylbutanamides
-
Chemical and Pharmaceutical Bulletin p. 1570 - 1574
(2007/10/02)
- File number:1
-

- 105409-38-9
-
Desymmetrization of glycerol derivatives with peptide-based acylation catalysts
-
Organic Letters p. 3021 - 3023
(2007/10/03)
- File number:4
-

- 105409-40-3
-
Enzymatic synthesis of 2,3-O-isopropylidene-sn-glycerol, a chiral building block for platelet-activating factor
-
Chemical and Pharmaceutical Bulletin p. 3440 - 3444
(2007/10/02)
- File number:1
-

- 105409-41-4
-
Enzymatic synthesis of 2,3-O-isopropylidene-sn-glycerol, a chiral building block for platelet-activating factor
-
Chemical and Pharmaceutical Bulletin p. 3440 - 3444
(2007/10/02)
- File number:1
-

- 105409-91-4
-
Pyridine derivative and pharmaceutical containing the same
-
- File number:1
-

- 105410-38-6
-
Deep eutectic solvent mediated synthesis of 3,4-dihydropyrimidin-2(1H)-ones and evaluation of biological activities targeting neurodegenerative disorders
-
Bioorganic Chemistry
(2021/11/20)
- File number:4
-

- 105411-95-8
-
CARDIOVASCULAR ACTIVITY OF NITRO DERIVATIVES OF AZOLOPYRIMIDINE
-
Pharmaceutical Chemistry Journal p. 550 - 554
(2007/10/02)
- File number:3
-

- 105412-34-8
-
Three-component one-pot synthesis of unsymmetrical 1,4-dihydropyridine derivatives in aqueous media
-
Journal of Chemical Research p. 441 - 443
(2009/06/30)
- File number:2
-
