z-logo
Premium
Studies on sulfinatodehalogenation. XXVIII. The addition of polyfluoroalkyl iodides to olefins initiated by sodium disulfite
Author(s) -
Huang BingNan,
Wu FanHong
Publication year - 1993
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.19930110214
Subject(s) - chemistry , adduct , sodium , aqueous solution , sodium salt , radical , sodium iodide , medicinal chemistry , organic chemistry , inorganic chemistry
Polyfluoroalkyl iodides reacted with olefins in aqueous DMF solution of sodium disulfite under mild conditions to give the corresponding 1:1 adducts in good yields, providing a convenient polyfluoroalkylation method. This indicated that R F . radicals were formed in the reaction of polyfluoroalkyl iodides and sodium disulfite. A SET mechanism is proposed for the sulfinatodehalogenation reaction of sodium disulfite.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom