福田常彦 | Chemistry Laboratories Central Research Division Takeda Chemical Industries Ltd.

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著作論文

Chemical Synthesis and Adjuvant Activity of N-Acetylmuramyl-L-alanyl-D-isoglutamine (MDP) Analogs
The Use of N-Hydroxy-5-norbornene-2,3-dicarboximide Active Esters in Peptide Synthesis
Isobornyloxycarbonyl Function, a New Convenient Amino-Protecting Group in Peptide Synthesis. I. Synthesis and Properties of Isobornyloxycarbonylamino Acids
Synthesis of Some Di-and Tri-Substituted Analogs of Luteinizing Hormone Releasing Hormone (LH-RH)
Isobornyloxycarbonyl Function, a New Convenient Amino-Protecting Group in Peptide Synthesis.IV. Synthesis of Gonadotropin-Releasing Hormone (Gn-RH or LH-RH/FSH-RH)
New Protecting Groups for the Indole Ring of Tryptophan in Peptide Synthesis : 2,4,6-Trimethoxybenzenesulfonyl and 4-Methoxy-2,3,6-trimethylbenzenesulfonyl Groups
Synthesis of immunologically Active Muramyl Dipeptide Derivatives containing a Quinonyl Moiety via Aminoacyl Intermediates
Novel Quinonyl Derivatives of Muramyl Dipeptide Possessing Potent Antitumor Activity
Synthesis of the Nonatetracontapeptide corresponding to the Sequence proposed for Thymopoietin II

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