Syntheses with perfluoroalkyl iodides. Part II. Addition to non-conjugated alkadienes; cyclization of 1,6-heptadiene, and of 4-substituted 1,6-heptadienoic compounds: bis-allyl ether, ethyl diallylmalonate, N,N′-diallylamine and N-substituted diallylamines; and additions to homologous exo- and endocyclic alkenes, and to bicyclic alkenes-Reference-Cited by-同舟云学术

Syntheses with perfluoroalkyl iodides. Part II. Addition to non-conjugated alkadienes; cyclization of 1,6-heptadiene, and of 4-substituted 1,6-heptadienoic compounds: bis-allyl ether, ethyl diallylmalonate, N,N′-diallylamine and N-substituted diallylamines; and additions to homologous exo- and endocyclic alkenes, and to bicyclic alkenes

Published:1999-07 Issue:2 Volume:96 Page:101-127
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Brace Neal O.

Publisher

Elsevier BV

Subject

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

Reference98 articles.

1. Syntheses with perfluoroalkyl radicals from perfluoroalkyl iodides. A rapid survey of synthetic possibilities with emphasis on practical applications. Part one: alkenes, alkynes and allylic compounds

2. cyclization to a Five-Membered Ring in the Free-Radical Reaction of Iodoperfluoroalkanes with 1,6-Heptadiene

3. Cyclization Reactions of Perfluoroalkyl-Substituted Radicals

4. Cyclization reactions of 6-hepten-2-yl radicals, 1-trichloromethyl-6-hepten-2-yl radicals, and related compounds

5. Free-radical addition of iodoperfluoralkanes to terminal alkadienes. Relative reactivity as a function of chain length and reaction conditions

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