スポンサーリンク
Department of Medicinal Chemistry, Kyoto Pharmaceutical University | 論文
- TETRAFLUOROBORIC ACID, A USEFUL DEPROTECTING REAGENT IN PEPTIDE SYNTHESIS
- A FLUORIDE ION DEPROTECTION STRATEGY IN PEPTIDE SYNTHESIS. : COMBINATION WITH SELECTIVE DEPROTECTION USING THE DILUTE METHANESULFONIC ACID OF α-MAINO PROTECTING GROUPS
- RACEMIZATION-FREE SYNTHESIS OF C-TERMINAL CYSTEINE-PEPTIDE USING 2-CHLOROTRITYL RESIN
- Synthesis of Rat Brain Natriuretic Peptide 45 Using Tetrafluoroboric Acid Deprotection and Silyl Chloride Disulfide Formation
- KYNOSTATIN (KNI)-227 AND -272,HIGHLY POTENT ANTI-HIV AGENTS : CONFORMATIONALLY CONSTRAINED TRIPEPTIDE INHIBITORS OF HIV PROTEASE CONTAINING ALLOPHENYLNORSTATINE
- KNI-102,A NOVEL TRIPEPTIDE HIV PROTEASE INHIBITOR CONTAINING ALLOPHENYLNORSTATINE AS A TRANSITION-STATE MIMIC
- Solution-Phase Synthesis of α-Rat Atrial Natriuretic Peptide (α-rANP)
- Solution-Phase Synthesis of α-Human Atrial Natriuretic Peptide (α-hANP)
- Synthesis of HIV Protease Dipeptide Inhibitors and Prodrugs
- Studies on Peptides. CXX. Synthesis of Growth Hormone Releasing Factor (GRF-37-NH_2) and N^α-Biotinyl-GRF-44-NH_2
- Studies on Peptides. CXIX. Synthesis of Growth Hormone Releasing Factor (hpGRF-40-OH)
- Synthesis of Negamycin and Its Derivatives as Potential Therapeutic Agents for Duchenne Muscular Dystrophy
- P-296 DEVELOPMENT OF RESIN SUPPORTED EVANS-TYPE CHIRAL AUXILIARY FOR SOLID-PHASE ASYMMETRIC REACTION
- Modification of P4 Position in β-secretase (BACE1) Inhibitors Containing Phenylnorstatine
- Solution Syntheses of Two Enkephalin-Containing Peptides, Peptide E and Dynorphin(1-24), Using N^-(2,4,6-Triisopropylphenylsulfonyl)tryptophan
- SYNTHESIS OF A NEWLY ISOLATED OPIOID TRIDECAPEPTIDE, RIMORPHIN, FROM PITUITARY USING A TRIFLUOROACETIC ACID-THIOANISOLE DEPROTECTION SYSTEM
- Studies on Peptides. LXXXV. A New Deprotecting Procedure for p-Toluenesulfonyl and p-Methoxybenzenesulfonyl Groups from the N^-Function of Histidine
- Synthesis and Activity of C-Terminal Heptapeptides of Tachykinins and Bombesin-like Peptides
- Suppressing Effect of Thioanisole on a Side Reaction during the Acidolytic Cleavage of Protecting Groups of Tyrosine
- Studies on Peptides. CXVI. Synthesis of the Protected Docosapeptide Corresponding to the C-Terminal Portion of Human Growth Hormone Releasing Factor (GRF, Somatocrinin)
スポンサーリンク