328 results on '"Kojima, Naoto"'
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2. Temperature-dependent behavior of poly(N-isopropylacrylamide) brushes via neutron reflectometry
3. Thermoresponsive block-copolymer brush-modified interfaces for effective fabrication of hepatocyte sheets
4. Thermoresponsive mixed polymer brush to effectively control the adhesion and separation of stem cells by altering temperature
5. Cell death-inducing activities via Hsp inhibition of the sesquiterpenes isolated from Valeriana fauriei
6. Synthesis and cancer cell growth inhibition effects of acetogenin analogs bearing ethylene glycol units for enhancing the water solubility
7. Convergent synthesis of stereoisomers of THF ring moiety of acetogenin thiophene analogue and their antiproliferative activities against human cancer cell lines
8. Novel and practical asymmetric synthesis of β2,3-amino esters using asymmetric Michael addition of chiral amine
9. Thiophene Carboxamide Analogs with Long Alkyl Chains Comprising Ethylene Glycol Units Inhibit Glioblastoma Cell Proliferation by Activating AMPK
10. Facile synthesis of 5-alkoxy-4-aryltetrahydrofuran-2-one using hypervalent iodine reagents
11. Construction of pyrrolophenanthridinone scaffolds mediated by samarium(II) diiodide and access to natural product synthesis
12. Mechanistic aspects of asymmetric intramolecular Heck reaction involving dynamic kinetic resolution: flexible conformation of the cyclohexenylidene–benzene system
13. Synthesis of dansyl-labeled probe of thiophene analogue of annonaceous acetogenins for visualization of cell distribution and growth inhibitory activity toward human cancer cell lines
14. Synthesis of Acetogenin Analogs Comprising Pyrimidine Moieties Linked by Amine Bonds and Their Inhibitory Activity against Human Cancer Cell Lines
15. Structure–activity relations of leucine derivatives reveal critical moieties for cellular uptake and activation of mTORC1-mediated signaling
16. JCI‑20679 suppresses the proliferation of glioblastoma stem cells by activating AMPK and decreasing NFATc2 expression levels
17. First asymmetric total synthesis of (+)-taiwaniaquinol D and (−)-taiwaniaquinone D by using intramolecular Heck reaction
18. JCI-20679 suppresses autophagy and enhances temozolomide-mediated growth inhibition of glioblastoma cells
19. Thermoresponsive block copolymer brush for temperature-modulated hepatocyte separation
20. Structure–antitumor activity relationship of hybrid acetogenins focusing on connecting groups between heterocycles and the linker moiety
21. Chemical structures and induction of cell death via heat shock protein inhibition of the prenylated phloroglucinol derivatives isolated from Hypericum erectum
22. Construction of sulfur-containing compounds with anti-cancer stem cell activity using thioacrolein derived from garlic based on nature-inspired scaffolds
23. Convergent synthesis of fluorescence-labeled probes of Annonaceous acetogenins and visualization of their cell distribution
24. Structure–Activity Relationships of Thiophene Carboxamide Annonaceous Acetogenin Analogs: Shortening the Alkyl Chain in the Tail Part Significantly Affects Their Growth Inhibitory Activity against Human Cancer Cell Lines
25. Construction of Acyclic All-Carbon Quaternary Stereocenter Based on Asymmetric Michael Addition of Chiral Amine
26. Application of a novel chromophoric reagent, 2,2′-binaphthyl-3,3′-dicarbonyl cyanide, to the absolute configuration determination of chiral secondary alcohols
27. Reaction of 3-Oxa-2-oxobicyclo[4.2.0]oct-4-ene-1-carboxylate with Dimethylsulfoxonium Methylide
28. [2+2]Photocycloaddition of 5,6-Substituted 2-Oxo-2H-pyran-3-carboxylates with Alkenes
29. Syntheses of C2′-Fluorinated Analogs of Solamin
30. Chemical structures and cytotoxic activities of the constituents isolated from Hibiscus tiliaceus
31. Facile Preparation of 2-Oxo-2H-1-pyran-3-carboxylates with the Electron-Withdrawing Group at the 5-Position
32. C(sub)2-symmetric bis-sulfoxide: a novel chiral auxiliary for asymmetric desymmetrization of cyclic meso-1,2-diols
33. Determination of the absolute stereochemistry and asymmetric total synthesis of madindolines A and B: a practical improvement to a second-generation approach from the first-generation
34. A write head integrated with a solid-immersion-lens system for heat-assisted magnetic recording
35. A Facile and Convenient Synthesis of Trisubstituted (E)-α,β-Unsaturated Esters by Tandem Acetylation-E1cB Reaction
36. Antimutagenic activity of ent-kaurane diterpenoids from the aerial parts of Isodon japonicus
37. Flying characteristics of a novel negative pressure slider 'Papillon.'(Proceedings of the 41st Annual Conference on Magnetism and Magnetic Materials)
38. Chemical Structures of Novel Maillard Reaction Products under Hyperglycemic Conditions
39. What Mary Knew : The Location of the Reader in Charles Brockden Brown’s Edgar Huntly
40. Skeletal transformation of α-pyrones having electron-withdrawing groups at 3,5-positions into ring-fused dihydrofurans
41. Asymmetric total synthesis of (+)-hexachlorosulfolipid, a cytotoxin isolated from Adriatic mussels
42. The Author's Metamorphosis : The Location of 'the Author' in John Barth's LETTERS
43. Novel and practical asymmetric synthesis of β 2,3 -amino esters using asymmetric Michael addition of chiral amine
44. A Simple and Rapid LC–MS/MS Method for Quantitation of Luseogliflozin in Rat Plasma and its Application to A PK Study
45. Thiophene-3-carboxamide analogue of annonaceous acetogenins as antitumor drug lead
46. Skeleton transformation of α-pyrone induced by 5-aryl substituent into ring-fused dihydrofuran
47. Structure–activity relationships of hybrid annonaceous acetogenins: Powerful growth inhibitory effects of their connecting groups between heterocycle and hydrophobic carbon chain bearing THF ring on human cancer cell lines
48. Critical role of a methyl group on the γ-lactone ring of annonaceous acetogenins in the potent inhibition of mitochondrial complex I
49. A novel thiophene‐3‐carboxamide analog of annonaceous acetogenin exhibits antitumor activity via inhibition of mitochondrial complex I
50. Construction of Seven Contiguous Chiral Centers by Two Methods: Quadruple Michael Addition vs Stepwise Double-Double Michael Addition Controlled by Adding Speed of Michael Acceptor
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