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

Takamasa Tanabe, Rika Obata, Shigeru Nishiyama

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)113-118
Number of pages6
JournalHeterocycles
Volume69
Issue number1
Publication statusPublished - 2006 Dec 1

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Thallium
Cyclization
Ions
Electrochemical oxidation
Biological Products
Oxidation
isodityrosine

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Oxidative cyclization of isodityrosine tripeptides : optimized condition and application of electrochemically generated thallium(III) ion. / Tanabe, Takamasa; Obata, Rika; Nishiyama, Shigeru.

In: Heterocycles, Vol. 69, No. 1, 01.12.2006, p. 113-118.

Research output: Contribution to journalArticle

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