- 24686-27-9
-
The synthesis of 9,10-dihydro-9-,10-(methaniminomethano)anthracene and N-protected derivatives via double reductive amination
-
Synthetic Communications p. 3481 - 3489
(2007/10/03)
- File number:2
-
- 247035-46-7
-
Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part 2: Synthesis of potent αvβ3/αIIbβ3 dual antagonists
-
Bioorganic and Medicinal Chemistry p. 2109 - 2130
(2007/10/03)
- File number:2
-
- 247128-20-7
-
From a Tb3+ chelated compound to a hybrid material: Selective emission responses to anions
-
Chemical Papers p. 221 - 225
(2015/03/03)
- File number:2
-
- 2475-78-7
-
1,2,5-THIAZOLIDINE DERIVATIVES USEFUL FOR TREATING CONDITIONS MEDIATED BY PROTEIN TYROSINE PHOSPHATASES (PTPASE)
-
- File number:2
-
- 2504147-16-2
-
Multicomponent one-pot procedure for the synthesis of free α-chiral amines from aldehydes
-
Journal of Organic Chemistry p. 10864 - 10867
(2007/10/03)
- File number:2
-
- 252004-41-4
-
HISTONE DEMETHYLASE INHIBITORS
-
- File number:2
-
- 253265-98-4
-
Discovery and selection of TMC114, a next generation HIV-1 protease inhibitor
-
Journal of Medicinal Chemistry p. 1813 - 1822
(2007/10/03)
- File number:2
-
- 257864-14-5
-
Palladium/P(t-Bu)3-catalyzed synthesis of aryl t-butyl ethers and application to the first synthesis of 4-chlorobenzofuran
-
Tetrahedron Letters p. 8837 - 8840
(2007/10/03)
- File number:2
-
- 25854-39-1
-
α-Nitrohydrazones: Versatile intermediates for phosphonate derivatives formation from primary nitro compounds
-
Tetrahedron Letters p. 2037 - 2038
(2007/10/03)
- File number:2
-
- 2593254-90-9
-
Discovery and Optimization of Small-Molecule Ligands for V-Domain Ig Suppressor of T-Cell Activation (VISTA)
-
Journal of the American Chemical Society p. 16194 - 16198
(2020/10/26)
- File number:2
-
- 263022-03-3
-
Discovery of N-(2-phenyl-1H-benzo[d]imidazol-5-yl)quinolin-4-amine derivatives as novel VEGFR-2 kinase inhibitors
-
European Journal of Medicinal Chemistry p. 698 - 707
(2014/08/18)
- File number:2
-
- 26629-10-7
-
CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES
-
Tetrahedron Letters p. 6109 - 6112
(2007/10/02)
- File number:2
-
- 267643-79-8
-
2-PHENYL-3H-IMIDAZO[4,5-B]PYRIDINE DERIVATES USEFUL AS INHIBITORS OF MAMMALIAN TYROSINE KINASE ROR1 ACTIVITY
-
- File number:2
-
- 27168-28-1
-
Novel Inhibitors of Human Renin. Cyclic Peptides Based on the Tetrapeptide Sequence Glu-D-Phe-Lys-D-Trp
-
Journal of Medicinal Chemistry p. 2552 - 2560
(2007/10/02)
- File number:2
-
- 27242-80-4
-
Synthesis and in vitro anticancer evaluation of 1,4-phenylene-bis-pyrimidine-2-amine derivatives
-
Turkish Journal of Chemistry p. 263 - 271
(2017/05/29)
- File number:2
-
- 27247-34-3
-
A predictive model for additions to: N -alkyl pyridiniums
-
Chemical Communications p. 2693 - 2696
(2021/03/18)
- File number:2
-
- 27318-84-9
-
SYNTHESIS OF TETRIARY PHOSPHINES AND PHOSPHINE OXIDES BY NUCLEOPHILIC ADDITION REACTIONS USING INTERFACIAL CATALYSTS OR SUPERBASIC MEDIA
-
Journal of general chemistry of the USSR p. 2197 - 2203
(2007/10/02)
- File number:2
-
- 27336-61-4
-
Rigid core vinamidinium salts and their N,N′-rotamers
-
Journal of Organic Chemistry p. 3099 - 3105
(2007/10/03)
- File number:2
-
- 27353-45-3
-
Synthesis of phenanthridinones via palladium-catalyzed C(sp2)-H aminocarbonylation of unprotected o-arylanilines
-
Chemical Communications p. 173 - 175
(2013/02/23)
- File number:2
-
- 27376-51-8
-
One-pot synthesis, spectroscopic characterizations, quantum chemical calculations, docking and cytotoxicity of 1-((dibenzylamino)methyl)pyrrolidine-2,5-dione
-
Journal of Molecular Structure
(2019/12/11)
- File number:2
-
- 274689-93-9
-
Organic reactions catalyzed by methylrhenium trioxide: Reactions of ethyl diazoacetate and organic azides
-
Journal of the American Chemical Society p. 9901 - 9907
(2007/10/03)
- File number:2
-
- 278780-85-1
-
New '2-phenylnaphthalene'-mediated synthesis of benzo[b]naphtho[2,3-d] furan-6,11-diones and 6-oxa-benzo[a]anthracene-5,7,12-triones: First total synthesis of 6-oxa-benzo[a]anthracen-5-ones
-
Tetrahedron p. 1353 - 1362
(2007/10/03)
- File number:2
-
- 279251-10-4
-
Design, Synthesis, and Evaluation of the Highly Selective and Potent G-Protein-Coupled Receptor Kinase 2 (GRK2) Inhibitor for the Potential Treatment of Heart Failure
-
Journal of Medicinal Chemistry p. 6942 - 6990
(2017/09/07)
- File number:2
-
- 280570-45-8
-
Isoquinoline and quinazoline urea analogues as antagonists for the human-adenosine A3 receptor
-
Journal of Medicinal Chemistry p. 2227 - 2238
(2007/10/03)
- File number:2
-
- 281232-88-0
-
SUBSTITUTED (AMINOIMINOMETHYL OR AMINOMETHYL) BENZOHETEROARYL COMPOUNDS
-
- File number:2
-
- 28190-63-8
-
Destructive nitration of polynitro carbonyl compounds III. Synthesis of 2,2,3,3,3-pentanitropropylnitrobenzenes and 2,2,3,3,3-pentanitropropyl-N-nitroaniline
-
Russian Journal of Organic Chemistry p. 1601 - 1604
(2007/10/03)
- File number:2
-
- 28230-40-2
-
A new amide protecting group
-
Chemische Berichte p. 2041 - 2051
(2007/10/05)
- File number:2
-
- 284022-81-7
-
Copper catalyzed conjugate addition of highly functionalized arylmagnesium compounds to enones
-
Tetrahedron p. 2727 - 2731
(2007/10/03)
- File number:2
-
- 290366-76-6
-
Asymmetric synthesis of piperidines using the nitro-Mannich reaction☆
-
- File number:2
-
- 293761-91-8
-
Oxygen-containing five-membered heterocyclic compound, synthesis method, pharmaceutical composition and application
-
- File number:2
-
- 29520-14-7
-
The preparation method of the overall tablet sizes hydrochloride (by machine translation)
-
- File number:2
-
- 298688-65-0
-
Polyhydroxypyrrolidine glycosidase inhibitors related to (+)-lentiginosine1
-
Journal of Carbohydrate Chemistry p. 585 - 601
(2007/10/03)
- File number:2
-
- 29974-68-3
-
OXIDATION OF N-ALKYL-N'-TOSYLHYDRAZINES WITH BROMINE
-
Tetrahedron p. 4097 - 4102
(2007/10/02)
- File number:2
-
- 299928-38-4
-
Identification of a Water-Soluble Indirubin Derivative as Potent Inhibitor of Insulin-like Growth Factor 1 Receptor through Structural Modification of the Parent Natural Molecule
-
Journal of Medicinal Chemistry p. 4949 - 4962
(2017/06/28)
- File number:2
-
- 300354-18-1
-
Heteroaromatic glucokinase activators
-
- File number:2
-
- 3005-72-9
-
Mapping the landscape of potentially primordial informational oligomers: (3′→2′)-D-phosphoglyceric acid linked acyclic oligonucleotides tagged with 2,4-disubstituted 5-aminopyrimidines as recognition elements
-
Chemistry - An Asian Journal p. 1252 - 1262
(2011/12/14)
- File number:2
-
- 300707-60-2
-
Investigation of the synthetic and mechanistic aspects of the highly stereoselective transformation of α-thioamides to α-thio-β- chloroacrylamides
-
Organic and Biomolecular Chemistry p. 1228 - 1241
(2008/02/03)
- File number:2
-
- 30085-94-0
-
Characterization and interconversions of 2-S-ethyl-2-thio-D-mannose diethyl dithioacetal and the facile epimerization of 2-thio-D-mannopyranose derivatives
-
Carbohydrate Research p. 53 - 71
(2007/10/03)
- File number:2
-
- 301206-01-9
-
Synthesis and biological evaluation of CX-659S and its related compounds for their inhibitory effects on the delayed-type hypersensitivity reaction
-
Bioorganic and Medicinal Chemistry p. 2037 - 2047
(2007/10/03)
- File number:2
-
- 301222-77-5
-
Novel, selective indole-based ECE inhibitors: Lead optimization via solid-phase and classical synthesis
-
Bioorganic and Medicinal Chemistry Letters p. 4201 - 4205
(2007/10/03)
- File number:2
-
- 301226-53-9
-
Process for the preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carbocyclic acids
-
- File number:2
-
- 302900-97-6
-
Processes and intermediates for the preparation of piperazine derivatives
-
- File number:2
-
- 302936-17-0
-
Discovery of Potent Small-Molecule SIRT6 Activators: Structure-Activity Relationship and Anti-Pancreatic Ductal Adenocarcinoma Activity
-
Journal of Medicinal Chemistry p. 10474 - 10495
(2020/11/02)
- File number:2
-
- 303064-94-0
-
Novel compounds that are inhibitors of YAP/TAZ-TEAD interaction and their use in the treatment of malignant mesothelioma
-
- File number:2
-
- 303163-16-8
-
Novel inhibitor of p38 MAP kinase as an anti-TNF-α drug: Discovery of N-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]benzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent
-
Journal of Medicinal Chemistry p. 5966 - 5979
(2007/10/03)
- File number:2
-
- 30345-85-8
-
β-Lactam via N-silylcarbodiimides
-
Liebigs Annalen der Chemie p. 1193 - 1204
(2007/10/02)
- File number:2
-
- 30361-99-0
-
Polar Hinges as Functionalized Conformational Constraints in (Bi)cyclic Peptides
-
ChemBioChem p. 387 - 395
(2017/02/24)
- File number:2
-
- 304008-29-5
-
Discovery of Lu AA33810: A highly selective and potent NPY5 antagonist with in vivo efficacy in a model of mood disorder
-
Bioorganic and Medicinal Chemistry Letters p. 5436 - 5441
(2011/10/12)
- File number:2
-
- 304452-55-9
-
Hedgehog pathway inhibitors of the acylthiourea and acylguanidine class show antitumor activity on colon cancer in vitro and in vivo
-
European Journal of Medicinal Chemistry p. 368 - 379
(2018/08/17)
- File number:2
-