- 10341-17-0
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Ionic reagent for controlling the gas-phase fragmentation reactions of cross-linked peptides
-
Analytical Chemistry p. 9279 - 9287
(2009/06/20)
- File number:1
-

- 103411-90-1
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SYNTHESIS OF (-)-DIHYDROMAHUBANOLIDE B AND (-)-ISODIHYDROMAHUBANOLIDE B
-
Chemistry Letters p. 319 - 322
(2007/10/02)
- File number:3
-

- 103412-29-9
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Structures of ent-Herbertane Sesquiterpenoids displaying Antifungal Properties from the Liverwort Herberta adunca
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Journal of the Chemical Society. Perkin transactions I p. 701 - 710
(2007/10/02)
- File number:1
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- 10341-25-0
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One-pot synthesis of permethylated α-CD-based rotaxanes having alkylene chain axles and their structural characteristics
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Chemistry Letters p. 806 - 808
(2012/09/22)
- File number:7
-

- 10341-26-1
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Photo-induced ring expansion of 1-triisopropylsilyloxy-1-azidocyclohexane: Preparation of ?-caprolactam [ 2H-Azepin-2-one, hexahydro- from Silane, [(1-azidocyclohexyl)oxy]tris(1-methylethyl)- ]
-
Organic Syntheses p. 165 - 165
(2017/09/14)
- File number:15
-

- 103412-68-6
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Novel, potent non-covalent thrombin inhibitors incorporating P3-lactam scaffolds
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Bioorganic and Medicinal Chemistry Letters p. 743 - 748
(2007/10/03)
- File number:7
-

- 10341-27-2
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Synthesis and Conformational Studies of Dipeptides Constrained by Disubstituted 3-(Aminoethoxy)propionic Acid Linkers
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Journal of Organic Chemistry p. 1716 - 1719
(2007/10/03)
- File number:4
-

- 103-41-3
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Oxidative esterification of aldehydes using mesoionic 1,2,3-triazolyl carbene organocatalysts
-
Organic Letters p. 3676 - 3679
(2014/08/05)
- File number:164
-

- 1034131-63-9
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AZAQUINOLONE BASED COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:2
-

- 1034131-89-9
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AZAQUINOLONE BASED COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:2
-

- 1034131-90-2
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AZAQUINOLONE BASED COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:2
-

- 1034132-07-4
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AZAQUINOLONE BASED COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
-
- File number:2
-

- 1034137-22-8
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The p: K a values of N-aryl imidazolinium salts, their higher homologues, and formamidinium salts in dimethyl sulfoxide
-
Organic and biomolecular chemistry p. 1910 - 1917
(2020/03/23)
- File number:3
-

- 103413-84-9
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Novel ferrocene-based 1,2,3-triazolyl compounds: Synthesis, anti-migration properties and catalytic effects on oxidizers during combustion
-
Inorganica Chimica Acta
(2019/12/26)
- File number:1
-

- 1034145-18-0
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Fluorine substitution-containing metal complex
-
- File number:2
-

- 10341-45-4
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Convenient Preparation of N-Acylbenzoxazines from Phenols, Nitriles, and DMSO Initiated by a Catalytic Amount of (COCl)2
-
Journal of Organic Chemistry p. 4932 - 4943
(2021/05/11)
- File number:2
-

- 103414-68-2
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An efficient synthetic route to novel 3-alkyl- and 3-aryl-4-iodophenols
-
Synthesis p. 221 - 224
(2008/12/20)
- File number:9
-

- 1034148-04-3
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Self-assembled asymmetric catalyst engaged in a continuous-flow platform: An anti -selective catalytic asymmetric nitroaldol reaction
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Organic Letters p. 3496 - 3499
(2014/07/21)
- File number:3
-

- 1034148-15-6
-
Discovery of indazole ethers as novel, potent, non-steroidal glucocorticoid receptor modulators
-
Bioorganic and Medicinal Chemistry Letters p. 5741 - 5748
(2016/11/28)
- File number:2
-

- 1034152-93-6
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Discovery of MK-7725, a potent, selective bombesin receptor subtype-3 agonist for the treatment of obesity
-
ACS Medicinal Chemistry Letters p. 252 - 256
(2012/07/13)
- File number:1
-

- 1034152-95-8
-
Discovery of MK-7725, a potent, selective bombesin receptor subtype-3 agonist for the treatment of obesity
-
ACS Medicinal Chemistry Letters p. 252 - 256
(2012/07/13)
- File number:1
-

- 1034156-00-7
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Self-assembled asymmetric catalyst engaged in a continuous-flow platform: An anti -selective catalytic asymmetric nitroaldol reaction
-
Organic Letters p. 3496 - 3499
(2014/07/21)
- File number:3
-

- 1034156-20-1
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Enantioselective synthesis of chiral β-aryloxy alcohols by ruthenium-catalyzed ketone hydrogenation via dynamic kinetic resolution (DKR)
-
Advanced Synthesis and Catalysis p. 81 - 84
(2010/06/16)
- File number:3
-

- 10341-59-0
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Synthesis of highly substituted pyrroles via nucleophilic catalysis
-
Journal of Organic Chemistry p. 6271 - 6274
(2010/11/19)
- File number:2
-

- 103416-88-2
-
Synthesis and structure-activity relationships of cis-tetrahydrophthalazinone/pyridazinone hybrids: A novel series of potent dual PDE3/PDE4 inhibitory agents
-
Journal of Medicinal Chemistry p. 2008 - 2016
(2007/10/03)
- File number:5
-

- 10341-75-0
-
Efficient and facile routes to nitrones
-
Organic Preparations and Procedures International p. 175 - 183
(2007/10/03)
- File number:68
-

- 103417-69-2
-
Design of an antithrombotic-antihypertensive agent (Wy 27569). Synthesis and evaluation of a series of 2-heteroaryl-substituted dihydropyridines
-
Journal of Medicinal Chemistry p. 646 - 652
(2007/10/02)
- File number:1
-

- 103417-72-7
-
Design of an antithrombotic-antihypertensive agent (Wy 27569). Synthesis and evaluation of a series of 2-heteroaryl-substituted dihydropyridines
-
Journal of Medicinal Chemistry p. 646 - 652
(2007/10/02)
- File number:1
-

- 103417-76-1
-
Design of an antithrombotic-antihypertensive agent (Wy 27569). Synthesis and evaluation of a series of 2-heteroaryl-substituted dihydropyridines
-
Journal of Medicinal Chemistry p. 646 - 652
(2007/10/02)
- File number:1
-

- 103417-86-3
-
Design of an antithrombotic-antihypertensive agent (Wy 27569). Synthesis and evaluation of a series of 2-heteroaryl-substituted dihydropyridines
-
Journal of Medicinal Chemistry p. 646 - 652
(2007/10/02)
- File number:1
-

- 103418-03-7
-
Nitrogen-substituted phenyl pyrrole compound and application thereof in plant sterilization
-
- File number:2
-

- 103418-06-0
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Tandem Michael addition/isocyanide insertion into the C-C bond: A novel access to 2-acylpyrroles and medium-ring fused pyrroles
-
Organic and Biomolecular Chemistry p. 7393 - 7399
(2013/10/22)
- File number:2
-

- 103418-56-0
-
DMF as Methine Source: Copper-Catalyzed Direct Annulation of Hydrazides to 1,3,4-Oxadiazoles
-
Advanced Synthesis and Catalysis p. 3986 - 3990
(2019/07/31)
- File number:7
-

- 1034186-48-5
-
An efficient approach for the synthesis of N-1 substituted hydantoins
-
European Journal of Organic Chemistry p. 1910 - 1916
(2009/04/04)
- File number:2
-

- 1034188-31-2
-
OXADIAZOLE DERIVATIVES AS S1P1 RECEPTOR AGONISTS
-
- File number:4
-

- 10341-88-5
-
Continuous flow synthesis of thieno[2,3-c ]isoquinolin-5(4 H)-one scaffold: A valuable source of PARP-1 inhibitors
-
Organic Process Research and Development p. 1345 - 1353
(2015/02/19)
- File number:10
-

- 1034189-07-5
-
CORTICOSTEROID LINKED BETA-AGONIST COMPOUNDS FOR USE IN THERAPY
-
- File number:3
-

- 10341-89-6
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NMR INVESTIGATION OF ARYL- AND BENZYL-MERCURIC COMPOUNDS; EXPERIMENTAL EVIDENCE FOR ?-? CONJUGATION INVOLVING THE CARBON-MERCURY BOND
-
Journal of Organometallic Chemistry p. 1 - 12
(2007/10/02)
- File number:3
-

- 1034190-08-3
-
Application of isotope-enriched 3-amino-1-propanesulfonic acid and derivative thereof
-
- File number:2
-

- 103419-18-7
-
Syntheses of (R)-(+)-cibenzoline and analogues via catalytic enantioselective cyclopropanation using (S)-phenylalanine-derived disulfonamide
-
Tetrahedron Asymmetry p. 3067 - 3069
(2007/10/03)
- File number:5
-

- 1034192-12-5
-
CYTOTOXIC PEPTIDES AND CONJUGATES THEREOF
-
- File number:7
-

- 103419-79-0
-
Designing Two-Dimensional Nanosheets for Improving Drug Delivery to Fucose-Receptor-Overexpressing Cancer Cells
-
ChemMedChem p. 2644 - 2652
(2018/12/11)
- File number:2
-

- 10342-06-0
-
Peptide synthesis in aqueous solution. IV. Preparation and properties of [p-(benzyloxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate, [p-(t-butoxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate and [p-(9-fluorenylmethyl-oxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate as water-soluble N-acylating reagents
-
Bulletin of the Chemical Society of Japan p. 3103 - 3108
(2007/10/02)
- File number:2
-

- 103420-77-5
-
An improved synthesis and resolution of 3-amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-ones
-
Journal of Organic Chemistry p. 730 - 734
(2007/10/02)
- File number:2
-

- 103420-78-6
-
Methods for Drug Discovery: Development of Potent, Selective, Orally Effecive Cholecystokinin Antagonists
-
Journal of Medicinal Chemistry p. 2235 - 2246
(2007/10/02)
- File number:1
-

- 103420-80-0
-
Methods for Drug Discovery: Development of Potent, Selective, Orally Effecive Cholecystokinin Antagonists
-
Journal of Medicinal Chemistry p. 2235 - 2246
(2007/10/02)
- File number:1
-

- 103420-82-2
-
Methods for Drug Discovery: Development of Potent, Selective, Orally Effecive Cholecystokinin Antagonists
-
Journal of Medicinal Chemistry p. 2235 - 2246
(2007/10/02)
- File number:2
-

- 103421-59-6
-
Methods for Drug Discovery: Development of Potent, Selective, Orally Effecive Cholecystokinin Antagonists
-
Journal of Medicinal Chemistry p. 2235 - 2246
(2007/10/02)
- File number:1
-

- 103421-60-9
-
Methods for Drug Discovery: Development of Potent, Selective, Orally Effecive Cholecystokinin Antagonists
-
Journal of Medicinal Chemistry p. 2235 - 2246
(2007/10/02)
- File number:1
-

- 103421-61-0
-
Discovery of clinical candidate BMS-906024: A potent pan-notch inhibitor for the treatment of leukemia and solid tumors
-
ACS Medicinal Chemistry Letters p. 523 - 527
(2015/05/27)
- File number:15
-
