The preparation and reactions of 1,3,4,5,6,7,8-heptafluoro-2-naphthyl prop-2-enyl ether: Formation of 1,3,4,5,6,7,8-heptafluoro-1-(prop-2-enyl)naphthalen-2-one and the photolysis and pyrolysis of this ketone [1].-Reference-Cited by-同舟云学术

The preparation and reactions of 1,3,4,5,6,7,8-heptafluoro-2-naphthyl prop-2-enyl ether: Formation of 1,3,4,5,6,7,8-heptafluoro-1-(prop-2-enyl)naphthalen-2-one and the photolysis and pyrolysis of this ketone [1].

Published:1980-11 Issue:5 Volume:16 Page:461-477
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Brooke Gerald M.,Matthews Raymond S.,Robson Nigel S.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference13 articles.

1. A new route to the rare tricyclo[3.3.1.02,7]nonane skeleton. Synthesis of 1,2,3,4,7-pentafluorotricyclo[3.3.1.02,7]non-3-ene-8,8-diol hemihydrate via thermolysis of pentafluorophenyl prop-2-enyl ether, and related studies

2. The pyrolysis of pentafluorophenyl allyl ether : the formation of a stable cyclohexa-2,5-dienone

3. 36. Polycyclic fluoroaromatic compounds. Part I. Some reactions of octafluoronaphthalene

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1. The preparation and properties of polyfluoro aromatic and heteroaromatic compounds;Journal of Fluorine Chemistry;1997-10

2. [3,3]-Sigmatropic rearrangements of fluorinated compounds;Journal of Fluorine Chemistry;1992-02

3. The preparation and thermolysis reactions of allyl 3,4,5,6,7,8- hexafluoroquinolin-2-yl ether, allyl 2,3,5,6,7,8- hexafluoroquinolin-4-yl ether and allyl 3,4,5,6,7,8- hexafluoroisoquinolin-1-yl ether.;Journal of Fluorine Chemistry;1988-03

4. Photochemistry of 1-allyl-naphthalen-2(1H)-ones: A revised mechanism for the formation of benzotricyclo[3.3.1.02,7]nonen-8-ones.;Tetrahedron Letters;1987-01

5. Reactions of polyfluoro-arenols and -heteroarenols with activated dimethyl sulphoxide. Facile [2,3]-sigmatropic rearrangement reactions giving de-aromatised products;Journal of the Chemical Society, Perkin Transactions 1;1987