Unique radical addition reactions onto perfluoro-enol esters

Ta i. Narita; Tokio Hagiwara; Hiroshi Hamana; Katsuhiko Tomooka; Yu Zhong Liu; Takeshi Nakai

doi:10.1016/0040-4039(95)01211-Y

Unique radical addition reactions onto perfluoro-enol esters

Ta i. Narita
, Tokio Hagiwara
, Hiroshi Hamana
, Katsuhiko Tomooka
, Yu Zhong Liu
, Takeshi Nakai

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

33 被引用数 (Scopus)

抄録

2-Benzoyloxy-F-propene, an F-enol ester, is shown to serve as a good and selective acceptor towards nucleophilic radicals generated from cyclic ethers, alcohols, and alkyl iodides to afford the addition product. The scope and synthetic utility of the radical addition reaction are described.

本文言語	英語
ページ（範囲）	6091-6094
ページ数	4
ジャーナル	Tetrahedron Letters
巻	36
号	34
DOI	https://doi.org/10.1016/0040-4039(95)01211-Y
出版ステータス	出版済み - 8月 21 1995
外部発表	はい

!!!All Science Journal Classification (ASJC) codes

生化学
創薬
有機化学

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10.1016/0040-4039(95)01211-Y

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引用スタイル

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title = "Unique radical addition reactions onto perfluoro-enol esters",

abstract = "2-Benzoyloxy-F-propene, an F-enol ester, is shown to serve as a good and selective acceptor towards nucleophilic radicals generated from cyclic ethers, alcohols, and alkyl iodides to afford the addition product. The scope and synthetic utility of the radical addition reaction are described.",

author = "Narita, \{Ta i.\} and Tokio Hagiwara and Hiroshi Hamana and Katsuhiko Tomooka and Liu, \{Yu Zhong\} and Takeshi Nakai",

year = "1995",

month = aug,

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doi = "10.1016/0040-4039(95)01211-Y",

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journal = "Tetrahedron Letters",

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T1 - Unique radical addition reactions onto perfluoro-enol esters

AU - Narita, Ta i.

AU - Hagiwara, Tokio

AU - Hamana, Hiroshi

AU - Tomooka, Katsuhiko

AU - Liu, Yu Zhong

AU - Nakai, Takeshi

PY - 1995/8/21

Y1 - 1995/8/21

N2 - 2-Benzoyloxy-F-propene, an F-enol ester, is shown to serve as a good and selective acceptor towards nucleophilic radicals generated from cyclic ethers, alcohols, and alkyl iodides to afford the addition product. The scope and synthetic utility of the radical addition reaction are described.

AB - 2-Benzoyloxy-F-propene, an F-enol ester, is shown to serve as a good and selective acceptor towards nucleophilic radicals generated from cyclic ethers, alcohols, and alkyl iodides to afford the addition product. The scope and synthetic utility of the radical addition reaction are described.

UR - https://www.scopus.com/pages/publications/0029099047

UR - https://www.scopus.com/pages/publications/0029099047#tab=citedBy

U2 - 10.1016/0040-4039(95)01211-Y

DO - 10.1016/0040-4039(95)01211-Y

M3 - Article

AN - SCOPUS:0029099047

SN - 0040-4039

VL - 36

SP - 6091

EP - 6094

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 34

ER -

Unique radical addition reactions onto perfluoro-enol esters

抄録

!!!All Science Journal Classification (ASJC) codes

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