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

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

32 Citations (Scopus)

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.

Original language	English
Pages (from-to)	6091-6094
Number of pages	4
Journal	Tetrahedron Letters
Volume	36
Issue number	34
DOIs	https://doi.org/10.1016/0040-4039(95)01211-Y
Publication status	Published - Aug 21 1995
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/0040-4039(95)01211-Y

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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",

language = "English",

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number = "34",

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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.

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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

Abstract

All Science Journal Classification (ASJC) codes

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