- 103692-31-5
-
Synthesis and dopaminergic binding of 2-aryldopamine analogues: Phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes
-
Journal of Medicinal Chemistry p. 1904 - 1912
(2007/10/02)
- File number:1
-

- 103692-33-7
-
Synthesis and dopaminergic binding of 2-aryldopamine analogues: Phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes
-
Journal of Medicinal Chemistry p. 1904 - 1912
(2007/10/02)
- File number:1
-

- 103692-37-1
-
Synthesis and dopaminergic binding of 2-aryldopamine analogues: Phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes
-
Journal of Medicinal Chemistry p. 1904 - 1912
(2007/10/02)
- File number:1
-

- 103692-42-8
-
Synthesis and dopaminergic binding of 2-aryldopamine analogues: Phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes
-
Journal of Medicinal Chemistry p. 1904 - 1912
(2007/10/02)
- File number:1
-

- 1036926-74-5
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PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS
-
- File number:3
-

- 1036931-21-1
-
PREPARATION OF 3-AMINO-3-(CYCLOBUTYLMETHYL)-2-(HYDROXY)-PROPIONAMIDE HYDROCHLORIDE
-
- File number:1
-

- 103693-31-8
-
Synthesis and Transformations of 4,5-Dihydro-1,4-benzothiazepin-3(2H)-one Derivatives
-
Chemische Berichte p. 2904 - 2913
(2007/10/02)
- File number:1
-

- 103693-33-0
-
Synthesis and Transformations of 4,5-Dihydro-1,4-benzothiazepin-3(2H)-one Derivatives
-
Chemische Berichte p. 2904 - 2913
(2007/10/02)
- File number:1
-

- 103693-47-6
-
Synthesis and Transformations of 4,5-Dihydro-1,4-benzothiazepin-3(2H)-one Derivatives
-
Chemische Berichte p. 2904 - 2913
(2007/10/02)
- File number:1
-

- 103693-48-7
-
Synthesis and Transformations of 4,5-Dihydro-1,4-benzothiazepin-3(2H)-one Derivatives
-
Chemische Berichte p. 2904 - 2913
(2007/10/02)
- File number:1
-

- 103693-49-8
-
Synthesis and Transformations of 4,5-Dihydro-1,4-benzothiazepin-3(2H)-one Derivatives
-
Chemische Berichte p. 2904 - 2913
(2007/10/02)
- File number:1
-

- 1036939-38-4
-
Modulation of the activity of histone acetyltransferases by long chain alkylidenemalonates (LoCAMs)
-
Bioorganic and Medicinal Chemistry p. 3690 - 3701
(2011/08/03)
- File number:2
-

- 103694-26-4
-
1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS
-
- File number:7
-

- 103694-27-5
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Lewis acid-catalyzed synthesis of 4-aminopyrimidines: A scalable industrial process
-
Organic Process Research and Development p. 427 - 431
(2013/05/09)
- File number:5
-

- 103694-68-4
-
Pro-fragrant ionic liquids with stable hemiacetal motifs: Water-triggered release of fragrances
-
Chemical Communications p. 4455 - 4457
(2015/03/18)
- File number:2
-

- 103-69-5
-
Anchoring of Pd(ii) complex in functionalized MCM-41 as an efficient and recoverable novel nano catalyst in C-C, C-O and C-N coupling reactions using Ph3SnCl
-
RSC Advances p. 33212 - 33220
(2015/04/27)
- File number:466
-

- 1036959-23-5
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2 - substituted pyrrolidines compound, preparation method and its application in the preparation of the peculiar smell (by machine translation)
-
- File number:2
-

- 1036969-20-6
-
Antibody conjugates of 7-ethyl-10-hydroxycamptothecin (SN-38) for targeted cancer chemotherapy
-
Journal of Medicinal Chemistry p. 6916 - 6926
(2009/11/30)
- File number:1
-

- 103697-17-2
-
P-arylation of aryl halides by an environmentally compatible method
-
Canadian Journal of Chemistry p. 1280 - 1284
(2017/11/27)
- File number:10
-

- 10369-75-2
-
Novel acridine-triazenes as prototype combilexins: Synthesis, DNA binding, and biological activity
-
Journal of Medicinal Chemistry p. 3488 - 3501
(2007/10/02)
- File number:3
-

- 103698-09-5
-
The synthesis of β-nitropyridine compounds
-
Acta Chemica Scandinavica p. 141 - 144
(2007/10/03)
- File number:1
-

- 103698-10-8
-
Synthesis of novel 1,7-naphthyridines by Friedlaender condensation of pyridine substrates
-
Journal of Heterocyclic Chemistry p. 1383 - 1387
(2012/01/05)
- File number:4
-

- 10369-82-1
-
Stereospecific Palladium-Promoted Oxyamination of Alkenes
-
Journal of Organic Chemistry p. 2893 - 2898
(2007/10/02)
- File number:16
-

- 103698-26-6
-
Strategies towards the synthesis of 6-N,N-diethylcarbamyloxy-1,4-dimethoxy- 7-naphthylboronic acid
-
Synthetic Communications p. 3041 - 3057
(2008/02/12)
- File number:1
-

- 10369-83-2
-
Decomposition and stabilization of drugs. XVI. Structure and stability of aminoalkylesters. (8) (author's transl)
-
Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 12 - 17,16,17
(2007/10/05)
- File number:3
-

- 103698-37-9
-
Conversion of Hydroxyl Groups in Alcohols to Other Functional Groups with N-Hydroxy-2-thiopyridone, and Its Application to Dialkylamines and Thiols
-
Bulletin of the Chemical Society of Japan p. 57 - 67
(2007/10/02)
- File number:5
-

- 103698-39-1
-
Decarboxylative radical addition to vinylsulphones and vinylphosphonium bromide: Some further novel transformations of geminal (pyridine-2-thiyl) phenylsulphones
-
Tetrahedron p. 7091 - 7108
(2007/10/02)
- File number:2
-

- 103698-48-2
-
RADICAL ADDITION TO VINYL SULPHONES AND VINYL PHOSPHONIUM SALTS
-
Tetrahedron Letters p. 6349 - 6352
(2007/10/02)
- File number:1
-

- 1036990-21-2
-
The Design of Potent, Selective and Drug-Like RGD αvβ1 Small-Molecule Inhibitors Derived from non-RGD α4β1 Antagonists
-
ChemMedChem p. 1315 - 1320
(2019/07/09)
- File number:4
-

- 1036990-42-7
-
Iridium-catalyzed C-H borylation of pyridines
-
Organic and Biomolecular Chemistry p. 7318 - 7327
(2014/11/07)
- File number:6
-

- 1036990-62-1
-
BICYCLIC HETEROCYCLIC COMPOUNDS AS PROTEIN TYROSINE KINASE INHIBITORS
-
- File number:2
-

- 1036991-20-4
-
PYRAZOLOPYRIMIDIN-2-YL DERIVATIVES AS JAK INHIBITORS
-
- File number:4
-

- 1036991-24-8
-
Synthesis of biaryls through a one-pot tandem borylation/Suzuki-Miyaura cross-coupling reaction catalyzed by a palladacycle
-
European Journal of Organic Chemistry p. 595 - 603
(2012/03/09)
- File number:11
-

- 1036991-25-9
-
Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors
-
European Journal of Medicinal Chemistry p. 311 - 323
(2012/09/08)
- File number:5
-

- 1036991-40-8
-
NOVEL 4-(INDOL-3-YL)-PYRAZOLE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USE
-
- File number:2
-

- 10369-97-8
-
A novel and efficient strategy for the synthesis of various carbamates using carbamoyl chlorides under solvent-free and grinding conditions using microwave irradiation
-
Chinese Chemical Letters p. 883 - 886
(2012/08/28)
- File number:1
-

- 1037-02-1
-
Synthesis and evaluation of a series of novel imidazolidinone analogues of 6-aminoflavone as anticancer and anti-inflammatory agents
-
Medicinal Chemistry Research p. 5066 - 5075
(2013/09/23)
- File number:5
-

- 103702-31-4
-
Studies on 2(1H)-quinolinone derivatives as gastric antiulcer active agents. 2-(4-Chlorobenzoylamino)-3-[2(1H)-quinolinon-4-yl]propionic acid and related compounds
-
Chemical and Pharmaceutical Bulletin p. 3775 - 3786
(2007/10/02)
- File number:2
-

- 103702-40-5
-
Studies on 2(1H)-quinolinone derivatives as gastric antiulcer active agents. 2-(4-Chlorobenzoylamino)-3-[2(1H)-quinolinon-4-yl]propionic acid and related compounds
-
Chemical and Pharmaceutical Bulletin p. 3775 - 3786
(2007/10/02)
- File number:1
-

- 1037-05-4
-
Asymmetric reduction of racemic 2-isoxazolines
-
Tetrahedron Asymmetry p. 2519 - 2528
(2009/04/04)
- File number:5
-

- 103706-73-6
-
Photochemistry of Host-Guest Complexes. VIII . The Photoreaction of Pyrazinedicarbonitrile Derivatives Having a Crown Ether Moiety in the Presence of an ω-Diethylamino-1-alkanaminium Salt
-
Journal of Heterocyclic Chemistry p. 977 - 980
(2007/10/02)
- File number:1
-

- 1037072-57-3
-
Syntheses of cis- and trans-dibenzo-30-crown-10 derivatives via regioselective routes and their complexations with paraquat and diquat
-
Journal of Organic Chemistry p. 5872 - 5880
(2008/12/21)
- File number:3
-

- 1037075-45-8
-
Discovery of GSK2656157: An optimized PERK inhibitor selected for preclinical development
-
ACS Medicinal Chemistry Letters p. 964 - 968
(2013/10/22)
- File number:6
-

- 103-70-8
-
Reactions of N- or N'-Blocked N-acylureas with Amines
-
Archiv der Pharmazie p. 430 - 437
(2007/10/02)
- File number:478
-

- 103708-02-7
-
Heptafluoro-p-tolyl as a Selective Protecting Group for the Enone Function of Androst-4-ene-3,17-dione: Application to the Preparation of Deuterium-labelled Testosterone
-
Journal of the Chemical Society. Chemical communications p. 635 - 636
(2007/10/02)
- File number:2
-

- 1037082-28-2
-
Discovery of a Highly Potent, Selective, and Orally Bioavailable Macrocyclic Inhibitor of Blood Coagulation Factor VIIa-Tissue Factor Complex
-
Journal of Medicinal Chemistry p. 7125 - 7137
(2016/08/24)
- File number:4
-

- 103708-37-8
-
Toward a total synthesis of pristinamycin II(B); a chiron approach to a C-9/C-16 fragment
-
Tetrahedron Letters p. 3145 - 3148
(2007/10/03)
- File number:6
-

- 1037085-12-3
-
Highly efficient and versatile synthesis of polyarylfluorenes via Pd-catalyzed C-H bond activation
-
Organic Letters p. 4588 - 4591
(2009/12/09)
- File number:1
-

- 1037088-26-8
-
Atropisomer Control in Macrocyclic Factor VIIa Inhibitors
-
Journal of Medicinal Chemistry p. 4007 - 4018
(2016/05/19)
- File number:2
-
