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

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

Access to Document

10.3987/com-06-s(k)11

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

Mori, T., Miyagi, M., Suzuki, K., Shibasaki, M., Saikawa, Y., & Nakata, M. (2007). Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion. Heterocycles, 72, 275-291. https://doi.org/10.3987/com-06-s(k)11

@article{f90da36350f34e819c467537f827b462,

title = "Synthetic studies on chlorofusin: Synthesis of the cyclic peptide portion",

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.",

author = "Tomonori Mori and Marie Miyagi and Kengo Suzuki and Mitsuhito Shibasaki and Yoko Saikawa and Masaya Nakata",

year = "2007",

month = apr,

day = "13",

doi = "10.3987/com-06-s(k)11",

language = "English",

volume = "72",

pages = "275--291",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

}

TY - JOUR

T1 - Synthetic studies on chlorofusin

T2 - Synthesis of the cyclic peptide portion

AU - Mori, Tomonori

AU - Miyagi, Marie

AU - Suzuki, Kengo

AU - Shibasaki, Mitsuhito

AU - Saikawa, Yoko

AU - Nakata, Masaya

PY - 2007/4/13

Y1 - 2007/4/13

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=34547844059&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=34547844059&partnerID=8YFLogxK

U2 - 10.3987/com-06-s(k)11

DO - 10.3987/com-06-s(k)11

M3 - Article

AN - SCOPUS:34547844059

VL - 72

SP - 275

EP - 291

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

ER -