Construction of the [6-7-5-5] tetracyclic core of all the carbocyclic frameworks of yuzurimine-type alkaloids

Ichiro Hayakawa; Keisuke Niida; Hideo Kigoshi

doi:10.1039/c5cc03479e

Construction of the [6-7-5-5] tetracyclic core of all the carbocyclic frameworks of yuzurimine-type alkaloids

Ichiro Hayakawa, Keisuke Niida, Hideo Kigoshi

研究成果 › 査読

18 被引用数 (Scopus)

抄録

Yuzurimine-type alkaloids make up a sub-family of Daphniphyllum alkaloids structurally featuring a [6-7-5-5] tetracarbocyclic core framework. In this manuscript, we describe our construction of the [6-7-5-5] tetracarbocyclic core of yuzurimine-type alkaloids by using a unique in situ intramolecular Wittig reaction and Sm-mediated cyclization as key steps.

本文言語	English
ページ（範囲）	11568-11571
ページ数	4
ジャーナル	Chemical Communications
巻	51
号	58
DOI	https://doi.org/10.1039/c5cc03479e
出版ステータス	Published - 7月 25 2015

ASJC Scopus subject areas

触媒
電子材料、光学材料、および磁性材料
セラミックおよび複合材料
化学 (全般)
表面、皮膜および薄膜
金属および合金
材料化学

文献へのアクセス

10.1039/c5cc03479e

他のファイルとリンク

引用スタイル

@article{98d36498d44444309449de291ac4f50e,

title = "Construction of the [6-7-5-5] tetracyclic core of all the carbocyclic frameworks of yuzurimine-type alkaloids",

abstract = "Yuzurimine-type alkaloids make up a sub-family of Daphniphyllum alkaloids structurally featuring a [6-7-5-5] tetracarbocyclic core framework. In this manuscript, we describe our construction of the [6-7-5-5] tetracarbocyclic core of yuzurimine-type alkaloids by using a unique in situ intramolecular Wittig reaction and Sm-mediated cyclization as key steps.",

author = "Ichiro Hayakawa and Keisuke Niida and Hideo Kigoshi",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2015.",

year = "2015",

month = jul,

day = "25",

doi = "10.1039/c5cc03479e",

language = "English",

volume = "51",

pages = "11568--11571",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "58",

}

TY - JOUR

T1 - Construction of the [6-7-5-5] tetracyclic core of all the carbocyclic frameworks of yuzurimine-type alkaloids

AU - Hayakawa, Ichiro

AU - Niida, Keisuke

AU - Kigoshi, Hideo

N1 - Publisher Copyright: © The Royal Society of Chemistry 2015.

PY - 2015/7/25

Y1 - 2015/7/25

N2 - Yuzurimine-type alkaloids make up a sub-family of Daphniphyllum alkaloids structurally featuring a [6-7-5-5] tetracarbocyclic core framework. In this manuscript, we describe our construction of the [6-7-5-5] tetracarbocyclic core of yuzurimine-type alkaloids by using a unique in situ intramolecular Wittig reaction and Sm-mediated cyclization as key steps.

AB - Yuzurimine-type alkaloids make up a sub-family of Daphniphyllum alkaloids structurally featuring a [6-7-5-5] tetracarbocyclic core framework. In this manuscript, we describe our construction of the [6-7-5-5] tetracarbocyclic core of yuzurimine-type alkaloids by using a unique in situ intramolecular Wittig reaction and Sm-mediated cyclization as key steps.

UR - http://www.scopus.com/inward/record.url?scp=84936139186&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84936139186&partnerID=8YFLogxK

U2 - 10.1039/c5cc03479e

DO - 10.1039/c5cc03479e

M3 - Article

C2 - 26097917

AN - SCOPUS:84936139186

SN - 1359-7345

VL - 51

SP - 11568

EP - 11571

JO - Chemical Communications

JF - Chemical Communications

IS - 58

ER -

Construction of the [6-7-5-5] tetracyclic core of all the carbocyclic frameworks of yuzurimine-type alkaloids

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