Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion

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

doi:10.3987/com-06-s(k)11

Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion

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

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-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 language	English
Pages (from-to)	275-291
Number of pages	17
Journal	Heterocycles
Volume	72
DOIs	https://doi.org/10.3987/com-06-s(k)11
Publication status	Published - 2007 Apr 13

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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AU - Miyagi, Marie

AU - Suzuki, Kengo

AU - Shibasaki, Mitsuhito

AU - Saikawa, Yoko

AU - Nakata, Masaya

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