Solid phase synthesis of crystalline protected penta-L-tryptophan methyl esters.
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概要
- 論文の詳細を見る
Solid phase syntheses of protected tryptophan homo-oligomers were accomplished by utilizing dimethylphosphinothioyl(Mpt) group as an <I>N</I><SUP>α</SUP>-amino protecting group which was removed by treatment with triphenylphosphine dihydrochloride. By measurements of the ultraviolet and fluorescence spectra it was ascertained that no modification on the tryptophan indole ring had occurred during these syntheses.
- 公益社団法人 日本化学会の論文
著者
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IKEDA Shigeru
Department of Computer and Mathematical Sciences, Graduate School of Information Sciences, Tohoku Un
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Handa Takashi
Department of Chemistry Faculty of Science The University of Tokyo
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Ueki Masaaki
Department of Anesthesia, Nishiwaki Municipal Hospital:Department of Anesthesia and Perioperative Medicine, Kobe University
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