Synthesis of the spiroacetal parts of spirofungin A and B

Yuko Shimizu; Hiromasa Kiyota; Takayuki Oritani

doi:10.1016/S0040-4039(00)00371-3

Synthesis of the spiroacetal parts of spirofungin A and B

Yuko Shimizu, Hiromasa Kiyota, Takayuki Oritani

研究成果 › 査読

20 被引用数 (Scopus)

抄録

The C9-C20 spiroacetal parts of spirofungin A and B, antifungal antibiotics from Streptomyces violaceusniger Tu 4113, were synthesized simultaneously from (S)-citronellyl bromide and (±)-epoxy alcohol via alkyne-lactone coupling reaction and diastereomeric separation. (C) 2000 Elsevier Science Ltd.

本文言語	English
ページ（範囲）	3141-3144
ページ数	4
ジャーナル	Tetrahedron Letters
巻	41
号	17
DOI	https://doi.org/10.1016/S0040-4039(00)00371-3
出版ステータス	Published - 4月 22 2000
外部発表	はい

ASJC Scopus subject areas

生化学
創薬
有機化学

文献へのアクセス

10.1016/S0040-4039(00)00371-3

他のファイルとリンク

引用スタイル

@article{36581fbe6fe6450eaac20ceb57c39eb3,

title = "Synthesis of the spiroacetal parts of spirofungin A and B",

abstract = "The C9-C20 spiroacetal parts of spirofungin A and B, antifungal antibiotics from Streptomyces violaceusniger Tu 4113, were synthesized simultaneously from (S)-citronellyl bromide and (±)-epoxy alcohol via alkyne-lactone coupling reaction and diastereomeric separation. (C) 2000 Elsevier Science Ltd.",

keywords = "Antibiotics, Lactonization, Polyketides, Spiro compounds",

author = "Yuko Shimizu and Hiromasa Kiyota and Takayuki Oritani",

year = "2000",

month = apr,

day = "22",

doi = "10.1016/S0040-4039(00)00371-3",

language = "English",

volume = "41",

pages = "3141--3144",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "17",

}

TY - JOUR

T1 - Synthesis of the spiroacetal parts of spirofungin A and B

AU - Shimizu, Yuko

AU - Kiyota, Hiromasa

AU - Oritani, Takayuki

PY - 2000/4/22

Y1 - 2000/4/22

N2 - The C9-C20 spiroacetal parts of spirofungin A and B, antifungal antibiotics from Streptomyces violaceusniger Tu 4113, were synthesized simultaneously from (S)-citronellyl bromide and (±)-epoxy alcohol via alkyne-lactone coupling reaction and diastereomeric separation. (C) 2000 Elsevier Science Ltd.

AB - The C9-C20 spiroacetal parts of spirofungin A and B, antifungal antibiotics from Streptomyces violaceusniger Tu 4113, were synthesized simultaneously from (S)-citronellyl bromide and (±)-epoxy alcohol via alkyne-lactone coupling reaction and diastereomeric separation. (C) 2000 Elsevier Science Ltd.

KW - Antibiotics

KW - Lactonization

KW - Polyketides

KW - Spiro compounds

UR - http://www.scopus.com/inward/record.url?scp=0034701511&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034701511&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)00371-3

DO - 10.1016/S0040-4039(00)00371-3

M3 - Article

AN - SCOPUS:0034701511

SN - 0040-4039

VL - 41

SP - 3141

EP - 3144

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Synthesis of the spiroacetal parts of spirofungin A and B

抄録

ASJC Scopus subject areas

文献へのアクセス

他のファイルとリンク

フィンガープリント

引用スタイル