Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion

Tomonori Mori, Marie Miyagi, Kengo Suzuki, Mitsuhito Shibasaki, Yoko Saikawa, Masaya Nakata

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

The cyclic peptide portion of chlorofusin was synthesized by condensation of the five segments, d-Ada-OTMSE, Boc-l.-Orn(Cbz), Boc-l-Thr-l-Ala, l-Asn(Tr)-d-Asn(Tr)-d-Leu-OTMSE, and Boc-l-Thr-d-Leu, followed by cyclization at the amide bond between d-Ada and l-Orn.

Original languageEnglish
Pages (from-to)275-291
Number of pages17
JournalHeterocycles
Volume72
DOIs
Publication statusPublished - 2007 Apr 13

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion'. Together they form a unique fingerprint.

Cite this