赤路健一 | Department of Medicinal Chemistry, Kyoto Pharmaceutical University

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著作論文

A Synthetic Method Suitable for the Rapid Preparation of ^N-Labeled Dermorphin Analogue, H-Try-D-Met(O)-Phe-Gly-NH_2 (SD-62)
RATIONAL DESIGN AND SYNTHESIS OF A NOVEL CLASS OF ACTIVE SITE-TARGETED HIV PROTEASE INHIBITORS CONTAINING A HYDROXYMETHYLCARBONYL ISOSTERE. USE OF PHENYLNORSTATINE OR ALLOPHENYLNORSTATINE AS A TRANSITION-STATE MIMIC
NEW HYDROXYL PROTECTING GROUPS OF A SAFETY-CATCH TYPE REMOVABLE BY TEDUCTIVE ACIDOLYSIS
Fluoren-9-ylmethyloxycarbonyl (Fmoc) Amino Acid Chloride as an Efficient Reagent for Anchoring Fmoc Amino Acid to 4-Alkoxybenzyl Alcohol Resin
Deprotection of the S-Trimetylacetamidomethyl (Tacm) Group Using Silver Tetrafluoroborate : : Application to the Synthesis of Porcine Brain Natriuretic Peptide-32 (pBNP-32)
Solution-Phase Synthesis of Porcine Brain Natriuretic Peptide (pBNP) Using S-Trimethylacetamido-methylcysteine
Trimethylacetamidomethyl (Tacm) Group, a New Protecting Group for the Thiol Function of Cysteine
SYNTHESIS OF PORCINE BRAIN NATRIURETIC PEPTIDE-32 USING SILVER TETRAFLUOROBORATE AS A NEW DEPROTECTING REAGENT OF THE S-TRIMETHYLACETAMIDOMETHYL GROUP
EFFICIENT SOLID PHASE PEPTIDE SYNTHESIS ON A PHENACYL-RESIN BY A METHANESULFONIC ACID α-AMINO DEPROTECTING PROCEDURE
TETRAFLUOROBORIC ACID, A USEFUL DEPROTECTING REAGENT IN PEPTIDE SYNTHESIS
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)

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