Oxidative cyclization of isodityrosine tripeptides: optimized condition and application of electrochemically generated thallium(III) ion

Takamasa Tanabe; Rika Obata; Shigeru Nishiyama

doi:10.3987/com-06-s(o)39

Oxidative cyclization of isodityrosine tripeptides: optimized condition and application of electrochemically generated thallium(III) ion

Takamasa Tanabe, Rika Obata, Shigeru Nishiyama

人文社会学科

研究成果: Article › 査読

4 被引用数 (Scopus)

抄録

Thallium(III) trinitrate oxidation of the tripeptide, which was a synthetic precursor of the 17-membered isodityrosine natural product, eurypamide, was investigated to give the desired cyclized compound in 96% yield at best. In addition, the thallium(III) species generated by electrochemical oxidation of thallium(I) successfully produced the target compounds.

本文言語	English
ページ（範囲）	113-118
ページ数	6
ジャーナル	Heterocycles
巻	69
号	1
DOI	https://doi.org/10.3987/com-06-s(o)39
出版ステータス	Published - 2006 12月 1

ASJC Scopus subject areas

分析化学
薬理学
有機化学

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10.3987/com-06-s(o)39

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引用スタイル

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