木村徹 | Department of Medicinal Chemistry, Kyoto Pharmaceutical University

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著作論文

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
A FLUORIDE ION DEPROTECTION STRATEGY IN PEPTIDE SYNTHESIS. : COMBINATION WITH SELECTIVE DEPROTECTION USING THE DILUTE METHANESULFONIC ACID OF α-MAINO PROTECTING GROUPS

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