289 results on '"Matsugi, Masato"'
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2. 分子間および分子内フルオロフィリック効果を活用する有機合成
3. Practical Epoxidation of Olefins Using Air and Ubiquitous Iron-Based Fluorous Salen Complex.
4. Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags
5. Concise Synthesis of Peptide Analogs Using a Fluorous-Fmoc Protection Strategy
6. N-Methylated tetrapeptide synthesis via sequential filtration procedures based on TeflonTM immobilization utilizing the properties of fluorous 9-fluorenylmethyl ester
7. Development of efficient processes for multi-gram scale and divergent preparation of fluorous-Fmoc reagents
8. A comparative study of the asymmetric epoxidation of aromatic olefins using the first generation manganese salen epoxidation catalysts and their light fluorous variants: an interesting discovery on the use of benzotrifluoride as a cosolvent
9. Asymmetric Henry reaction using a double fluorous-tagged Co–salen complex
10. The systematic structure–activity relationship to predict how flavones bind to human androgen receptor for their antagonistic activity
11. Synthesis of carbamoyl azides via the Lossen rearrangement utilizing diphenyl phosphorazidate
12. A fluorous Mukaiyama coupling reagent for a concise condensation reaction: utility of medium-fluorous strategy
13. A solvent-free synthesis of 4-aryl-NH-1,2,3-triazoles from ketones utilizing diphenyl phosphorazidate
14. Synthesis of 1,5-Disubstituted Tetrazoles from Nitrones by Using Bis(p-nitrophenyl) Phosphorazidate in the Presence of 4-(Dimethylamino)pyridine
15. Cutting edge of diphenyl phosphorazidate (DPPA) as a synthetic reagent – A fifty-year odyssey
16. Synthesis of Carbamoyl Azides Via The Lossen Rearrangement Utilizing Diphenyl Phosphorazidate
17. A recyclable and highly stereoselective multi-fluorous proline catalyst for asymmetric aldol reactions
18. SNAr azidation of phenolic functions utilizing diphenyl phosphorazidate
19. A Fluorous Proline Catalyst Immobilized on Teflon® for Highly Stereoselective Asymmetric Aldol Reactions
20. Synthesis of 1,5-Disubstituted Tetrazoles from Nitrones by Using Bis(p -nitrophenyl) Phosphorazidate in the Presence of 4-(Dimethylamino)pyridine.
21. Facile and efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions
22. Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate
23. An Expeditious Approach to Tetrazoles from Amides Utilizing Phosphorazidates
24. Radical addition reaction of brominated active methylene compounds to enol ethers using 2,2'-azobis(2,4-dimethyl-4-methoxyvaleronitrile) (V-70) as an initiator
25. Asymmetric pummerer rearrangement and related reactions
26. A novel separation technique of diastereomeric esters of pyridylethanols by extraction: formal total synthesis of PNU-142721, HIV-1 reverse transcriptase inhibitor
27. An efficient methodology for the C–C bond forming radical cyclization of hydrophobic substrates in water: effect of additive on radical reaction in water
28. Unprecedented Asymmetric Epoxidation of Isolated Carbon-Carbon Double Bonds by a Chiral Fluorous Fe(III) Salen Complex: Exploiting Fluorophilic Effect for Catalyst Design
29. Pummerer rearrangement using bis(p-nitrophenyl) phosphorazidate as an azidation reagent: A novel synthesis of azidomethyl sulfides
30. Catalytic asymmetric oxidation of sulfide with titanium–mandelic acid complex: practical synthesis of ( S)-3-[1-(2-methylphenyl)imidazol-2-ylsulfinyl]propan-1-ol, the key intermediate of OPC-29030
31. Highly stereoselective synthesis of carbocycles via a radical addition reaction using 2,2'-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70L]
32. Polonovski-type reaction induced by O-silylated ketene acetals
33. Activation of Grubbs–Hoveyda Second-Generation Catalysts Employing Aromatic Ligands Bearing a Widespread Aryl Substituent
34. A Practical Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes Employing the Azide Anion from Diphenyl Phosphorazidate
35. Efficient stereoselective synthesis of α- C-glycopyranosides using 2,2′-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70]
36. Synthesis and RCM reactions using a recyclable grubbs-hoveyda metathesis catalyst activated by a light fluorous tag
37. SN2 displacement at the quaternary carbon center: a novel entry to the synthesis of α,α-disubstituted α-amino acids
38. A medium fluorous Grubbs–Hoveyda 2nd generation catalyst for phase transfer catalysis of ring closing metathesis reactions
39. Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis
40. Fluorous Mixture Synthesis of Tripeptides and Pentapeptides Using a Fluorous-Fmoc Protection Strategy
41. Grubbs–Hoveyda Second-Generation Catalysts Activated by the Introduction of a Light Fluorous Tag onto the Bidentate Ligands
42. Fluorous mixture synthesis of fluorous-Fmoc reagents using a one-pot double tagging strategy
43. Highly Activated Second-Generation Grubbs–Hoveyda Catalyst Driven by Intramolecular Steric Strain
44. Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes Using Diphenyl Phosphorazidate
45. ChemInform Abstract: SN2 Displacement at the Quaternary Carbon Center: A Novel Entry to the Synthesis of α,α-Disubstituted α-Amino Acids.
46. ChemInform Abstract: A Medium Fluorous Grubbs—Hoveyda 2nd Generation Catalyst for Phase Transfer Catalysis of Ring Closing Metathesis Reactions.
47. Concise Synthesis of All Stereoisomers of Dendroamide A by Fluorous Mixture Synthesis Based on Fluorous‐Fmoc Protection of Amino Acids
48. ChemInform Abstract: Enhancement of Stereoselectivities in Asymmetric Synthesis Using Fluorinated Solvents, Auxiliaries, and Catalysts
49. Enhancement of stereoselectivities in asymmetric synthesis using fluorinated solvents, auxiliaries, and catalysts
50. Liquid-Phase Split-Type Combinatorial Synthesis of Tripeptide Derivatives Encoded by Fluorous Fmoc Reagents
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