- 10387-93-6
-
Diastereoselective One-Pot Synthesis of Oxazolines Using Sulfur Ylides and Acyl Imines
-
Journal of Organic Chemistry p. 7219 - 7226
(2019/06/14)
- File number:7
-

- 103879-45-4
-
WDR5 INHIBITORS AND MODULATORS
-
- File number:3
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- 103879-58-9
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Widely Exploited, Yet Unreported: Regiocontrolled Synthesis and the Suzuki–Miyaura Reactions of Bromooxazole Building Blocks
-
European Journal of Organic Chemistry p. 2884 - 2898
(2019/03/07)
- File number:2
-

- 10388-19-9
-
SYNTHESIS OF BENZAMIDES, AND THEIR ANTISPASMODIC AND ANTIHYPOXIC PROPERTIES
-
Pharmaceutical Chemistry Journal p. 335 - 338
(2007/10/02)
- File number:27
-

- 10388-20-2
-
Facile iodination of aromatic compounds having electron-withdrawing substituents. Generation of triiodine cation in the system tetra-N- iodoglycoluril-iodine-sulfuric acid
-
Russian Journal of Organic Chemistry p. 935 - 936
(2009/06/08)
- File number:8
-

- 103882-03-7
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ISOLATION AND SYNTHESIS OF BISHORDENINYL TERPENE ALKALOIDS. SOME EXPERIMENTS RELATING TO THE NATURAL OCCURENCE OF FORMAL DIELS-ALDER ADDUCTS.
-
Tetrahedron p. 4309 - 4320
(2007/10/02)
- File number:1
-

- 103882-09-3
-
Cholecystokinin B antagonists. Synthesis and quantitative structure-activity relationships of a series of C-terminal analogues of CI-988
-
Bioorganic and Medicinal Chemistry p. 1733 - 1745
(2007/10/03)
- File number:19
-

- 103882-27-5
-
Analogues of σ receptor ligand 1-cyclohexyl-4-[3-(5-methoxy-1,2,3,4- tetrahydronaphthalen-1-yl)propyl]piperazine (PB28) with added polar functionality and reduced lipophilicity for potential use as positron emission tomography radiotracers
-
Journal of Medicinal Chemistry p. 1022 - 1032
(2011/04/26)
- File number:4
-

- 1038827-60-9
-
Hydroquinone-quinone oxidation by molecular oxygen: A simple tool for signal amplification through auto-generation of hydrogen peroxide
-
Organic and Biomolecular Chemistry p. 5074 - 5078
(2013/08/15)
- File number:5
-

- 1038827-63-2
-
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors
-
ACS Medicinal Chemistry Letters p. 359 - 362
(2015/03/30)
- File number:3
-

- 1038827-78-9
-
Efficacious inhaled PDE4 inhibitors with low emetic potential and long duration of action for the treatment of COPD
-
Journal of Medicinal Chemistry p. 4661 - 4676
(2014/07/07)
- File number:3
-

- 1038827-93-8
-
3-‘4-HETEROCYCLYL -1,2,3,-TRIAZOL-1-YL!-N-ARYL-BENZAMIDES AS INHIBITORS OF THE CYTOKINES PRODUCTION FOR THE TREATMENT OF CHRONIC INFLAMMATORY DISEASES
-
- File number:2
-

- 10388-28-0
-
Synthesis of novel molybdaboranes from (η5-C5R5)MoCl(n) precursors (R = H, Me; N = 1,2,4)
-
Journal of the American Chemical Society p. 2586 - 2598
(2007/10/03)
- File number:9
-

- 1038828-20-4
-
A mild and novel synthesis of functionalized fused imidazole analogues under environmentally benign reaction media
-
Tetrahedron Letters p. 3473 - 3477
(2014/06/10)
- File number:4
-

- 103882-85-5
-
Unprecedented gas-phase chiroselective logic gates
-
Organic and Biomolecular Chemistry p. 1717 - 1719
(2011/05/03)
- File number:58
-

- 103883-03-0
-
Conversion of procyanidin B-type (catechin dimer) to A-type: Evidence for abstraction of C-2 hydrogen in catechin during radical oxidation
-
Tetrahedron Letters p. 485 - 488
(2007/10/03)
- File number:5
-

- 103883-23-4
-
Simple and condensed β-lactams. Part 20. Reaction of some 1-(4-methoxyphenyl)azetidin-2-ones with cerium(IV) ammonium nitrate (CAN): Trapping of the quinone imine intermediate with chloride and iodide anions
-
Tetrahedron p. 4185 - 4200
(2007/10/02)
- File number:2
-

- 103883-24-5
-
Stereoselective reactions. IX. Synthetic studies on optically active β-lactams. I. Chiral synthesis of carbapenam and carbapenem ring systems starting from (S)-aspartic acid
-
Chemical and Pharmaceutical Bulletin p. 3299 - 3306
(2007/10/02)
- File number:1
-

- 10388-32-6
-
New nicotinic acid-based 3,5-diphenylpyrazoles: design, synthesis and antihyperlipidemic activity with potential NPC1L1 inhibitory activity
-
Molecular Diversity p. 673 - 686
(2020/02/25)
- File number:5
-

- 103883-91-6
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Effect of Halogen and of a Para Substituent on the Solid-State Conformation of Several Crowded Electrophilic Vinyl Halides
-
Journal of Organic Chemistry p. 4107 - 4111
(2007/10/02)
- File number:1
-

- 103884-34-0
-
Phase-Managed Organic Synthesis. A New Synthesis of Mixed Formic Anhydrides
-
Journal of Organic Chemistry p. 3744 - 3746
(2007/10/02)
- File number:4
-

- 10388-48-4
-
Cytotoxic triterpenoids from the leaves of Euphorbia pulcherrima
-
Planta Medica p. 322 - 325
(2007/10/03)
- File number:3
-

- 103884-97-5
-
9-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)guanine: A metabolically stable cytotoxic analogue of 2'-deoxyguanosine
-
Journal of Medicinal Chemistry p. 2389 - 2392
(2007/10/02)
- File number:8
-

- 103884-98-6
-
Synthesis and enzymatic resolution of carbocyclic 2'-ara-fluoro-guanosine: A potent new anti-herpetic agent
-
Journal of the Chemical Society. Chemical communications p. 656 - 658
(2007/10/02)
- File number:12
-

- 103884-99-7
-
9-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)guanine: A metabolically stable cytotoxic analogue of 2'-deoxyguanosine
-
Journal of Medicinal Chemistry p. 2389 - 2392
(2007/10/02)
- File number:1
-

- 103885-01-4
-
9-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)guanine: A metabolically stable cytotoxic analogue of 2'-deoxyguanosine
-
Journal of Medicinal Chemistry p. 2389 - 2392
(2007/10/02)
- File number:1
-

- 103885-02-5
-
9-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)guanine: A metabolically stable cytotoxic analogue of 2'-deoxyguanosine
-
Journal of Medicinal Chemistry p. 2389 - 2392
(2007/10/02)
- File number:1
-

- 103886-92-6
-
Conversion of amines to imines employing Polymer-Supported Sulfoxide (PSS) and Polymer-Supported Perruthenate (PSP): Synthesis of pyrrolo[2,1-c][1,4] benzodiazepines
-
Advanced Synthesis and Catalysis p. 249 - 254
(2007/10/03)
- File number:10
-

- 103887-32-7
-
A new solvent system (Cyclopentyl methyl ether-water) in process development of darifenacin HBr
-
Organic Process Research and Development p. 1591 - 1597
(2013/02/23)
- File number:18
-

- 103887-39-4
-
Synthesis of Arylethylamines via C(sp3)-C(sp3) Palladium-Catalyzed Cross-Coupling
-
Journal of Organic Chemistry p. 3583 - 3604
(2021/02/27)
- File number:18
-

- 103-88-8
-
In situ generated acylimidazolium acetate as an efficient catalyst and acylating agent for the acetylation of alcohols, phenols, and amines at ambient temperature
-
Cuihua Xuebao/Chinese Journal of Catalysis p. 1787 - 1790
(2013/10/21)
- File number:382
-

- 103888-42-2
-
Benzoic acid derivatives and their production
-
- File number:1
-

- 103889-79-8
-
Synthesis of Optically Active Arylglycines by Photolysis of Optically Active (β-Hydroxyamino) Carbene-Chromium(0) Complexes
-
Journal of Organic Chemistry p. 6914 - 6920
(2007/10/02)
- File number:1
-

- 103889-81-2
-
Synthesis of Optically Active Arylglycines by Photolysis of Optically Active (β-Hydroxyamino) Carbene-Chromium(0) Complexes
-
Journal of Organic Chemistry p. 6914 - 6920
(2007/10/02)
- File number:1
-

- 10388-98-4
-
Facile nucleophilic substitution of sulfonyl oxime ethers: An easy access to oxime ethers, carbonyl compounds and amines
-
Chemical Communications p. 7822 - 7824
(2010/11/19)
- File number:2
-

- 103889-84-5
-
A facile synthesis of substituted phenylglycines
-
Synthetic Communications p. 1095 - 1102
(2007/10/03)
- File number:6
-

- 103889-86-7
-
A practical asymmetric synthesis of homochiral α-arylglycines
-
Tetrahedron Asymmetry p. 149 - 155
(2007/10/03)
- File number:6
-

- 103890-69-3
-
Tandem nucleophilic addition-intramolecular aza-michael reaction: Facile synthesis of chiral fluorinated isoindolines
-
Organic Letters p. 5494 - 5497
(2011/02/23)
- File number:11
-

- 103890-70-6
-
Copper-Catalyzed One-Pot Cascade Cyclization for the Synthesis of Isoindolo[2,1-a]quinoxalines
-
Advanced Synthesis and Catalysis p. 4272 - 4276
(2021/08/03)
- File number:10
-

- 103890-73-9
-
On the mechanism of the dyotropic expansion of hydrindanes into decalins
-
Organic and Biomolecular Chemistry p. 1073 - 1079
(2022/02/16)
- File number:1
-

- 103890-78-4
-
THERAPY FOR COMPLICATIONS OF DIABETES
-
- File number:7
-

- 1038915-56-8
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:2
-

- 1038915-58-0
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:3
-

- 1038915-60-4
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:14
-

- 1038915-64-8
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:2
-

- 1038915-73-9
-
Process development of C-N cross-coupling and enantioselective biocatalytic reactions for the asymmetric synthesis of niraparib
-
Organic Process Research and Development p. 215 - 227
(2014/05/20)
- File number:6
-

- 1038915-90-0
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:5
-

- 1038915-92-2
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors
-
Journal of Medicinal Chemistry p. 7170 - 7185
(2010/07/04)
- File number:7
-

- 1038916-08-3
-
Development of a fit-for-purpose large-scale synthesis of an oral PARP inhibitor
-
Organic Process Research and Development p. 831 - 840
(2012/07/03)
- File number:3
-
