Phosphazenes with olefinic side groups: proton abstraction reactions of fluoroalkoxy derivatives

Harry R. Allcock; Paul R. Suszko; Thomas L. Evans

doi:10.1021/om00071a006

Phosphazenes with olefinic side groups: proton abstraction reactions of fluoroalkoxy derivatives

Harry R. Allcock, Paul R. Suszko, Thomas L. Evans

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

13 Scopus citations

Abstract

The cyclic phosphazenes N_aP_a(OPh)₅OCH₂CF_a, and [NP( OCH₂CF₃)₂]_a undergo dehydrofluorination and deprotonation when treated with n-butyllithium at -78 °C to form metalated

Original language	English (US)
Pages (from-to)	1443-1449
Number of pages	7
Journal	Organometalllics
Volume	1
Issue number	11
DOIs	https://doi.org/10.1021/om00071a006
State	Published - Jan 1 1982

All Science Journal Classification (ASJC) codes

Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1021/om00071a006

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@article{3716a8e8287342e78f72c2febe324f0d,

title = "Phosphazenes with olefinic side groups: proton abstraction reactions of fluoroalkoxy derivatives",

abstract = "The cyclic phosphazenes NaPa(OPh)5OCH2CFa, and [NP( OCH2CF3)2]a undergo dehydrofluorination and deprotonation when treated with n-butyllithium at -78 °C to form metalated",

author = "Allcock, {Harry R.} and Suszko, {Paul R.} and Evans, {Thomas L.}",

year = "1982",

month = jan,

day = "1",

doi = "10.1021/om00071a006",

language = "English (US)",

volume = "1",

pages = "1443--1449",

journal = "Organometallics",

issn = "0276-7333",

publisher = "American Chemical Society",

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TY - JOUR

T1 - Phosphazenes with olefinic side groups

T2 - proton abstraction reactions of fluoroalkoxy derivatives

AU - Allcock, Harry R.

AU - Suszko, Paul R.

AU - Evans, Thomas L.

PY - 1982/1/1

Y1 - 1982/1/1

N2 - The cyclic phosphazenes NaPa(OPh)5OCH2CFa, and [NP( OCH2CF3)2]a undergo dehydrofluorination and deprotonation when treated with n-butyllithium at -78 °C to form metalated

AB - The cyclic phosphazenes NaPa(OPh)5OCH2CFa, and [NP( OCH2CF3)2]a undergo dehydrofluorination and deprotonation when treated with n-butyllithium at -78 °C to form metalated

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U2 - 10.1021/om00071a006

DO - 10.1021/om00071a006

M3 - Article

AN - SCOPUS:0000851273

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EP - 1449

JO - Organometallics

JF - Organometallics

SN - 0276-7333

IS - 11

ER -

Phosphazenes with olefinic side groups: proton abstraction reactions of fluoroalkoxy derivatives

Abstract

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