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 |
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Pages (from-to) | 275-291 |
Number of pages | 17 |
Journal | Heterocycles |
Volume | 72 |
Publication status | Published - 2007 Apr 13 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
Synthetic studies on chlorofusin : Synthesis of the cyclic peptide portion. / Mori, Tomonori; Miyagi, Marie; Suzuki, Kengo; Shibasaki, Mitsuhito; Saikawa, Yoko; Nakata, Masaya.
In: Heterocycles, Vol. 72, 13.04.2007, p. 275-291.Research output: Contribution to journal › Article
}
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
M3 - Article
AN - SCOPUS:34547844059
VL - 72
SP - 275
EP - 291
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
ER -