Total synthesis of (-)-stevastelin B

Kazuo Kurosawa; Toshihiko Nagase; Noritaka Chida

doi:10.1039/b202298b

Total synthesis of (-)-stevastelin B

Kazuo Kurosawa, Toshihiko Nagase, Noritaka Chida

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

Abstract

The total synthesis and an unambiguous structure confirmation of stevastelin B 1, a novel 15-membered cyclic depsipeptide, are described; the fatty acid moiety in 1, prepared stereoselectively from L-quebrachitol was converted into the amino carboxylic acid, whose macrolactamization by Shioiri's procedure effectively constructed the cyclic structure of 1.

Original language	English
Pages (from-to)	1280-1281
Number of pages	2
Journal	Chemical Communications
Volume	2
Issue number	12
DOIs	https://doi.org/10.1039/b202298b
Publication status	Published - 2002 Jan 1

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

Access to Document

10.1039/b202298b

Cite this

@article{e96b8d8227ad4455a2c10f5fee0f99b8,

title = "Total synthesis of (-)-stevastelin B",

abstract = "The total synthesis and an unambiguous structure confirmation of stevastelin B 1, a novel 15-membered cyclic depsipeptide, are described; the fatty acid moiety in 1, prepared stereoselectively from L-quebrachitol was converted into the amino carboxylic acid, whose macrolactamization by Shioiri's procedure effectively constructed the cyclic structure of 1.",

author = "Kazuo Kurosawa and Toshihiko Nagase and Noritaka Chida",

year = "2002",

month = jan,

day = "1",

doi = "10.1039/b202298b",

language = "English",

volume = "2",

pages = "1280--1281",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "12",

}

TY - JOUR

T1 - Total synthesis of (-)-stevastelin B

AU - Kurosawa, Kazuo

AU - Nagase, Toshihiko

AU - Chida, Noritaka

PY - 2002/1/1

Y1 - 2002/1/1

N2 - The total synthesis and an unambiguous structure confirmation of stevastelin B 1, a novel 15-membered cyclic depsipeptide, are described; the fatty acid moiety in 1, prepared stereoselectively from L-quebrachitol was converted into the amino carboxylic acid, whose macrolactamization by Shioiri's procedure effectively constructed the cyclic structure of 1.

AB - The total synthesis and an unambiguous structure confirmation of stevastelin B 1, a novel 15-membered cyclic depsipeptide, are described; the fatty acid moiety in 1, prepared stereoselectively from L-quebrachitol was converted into the amino carboxylic acid, whose macrolactamization by Shioiri's procedure effectively constructed the cyclic structure of 1.

UR - http://www.scopus.com/inward/record.url?scp=0036266821&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0036266821&partnerID=8YFLogxK

U2 - 10.1039/b202298b

DO - 10.1039/b202298b

M3 - Article

C2 - 12109115

AN - SCOPUS:0036266821

SN - 1359-7345

VL - 2

SP - 1280

EP - 1281

JO - Chemical Communications

JF - Chemical Communications

IS - 12

ER -

Total synthesis of (-)-stevastelin B

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this