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Fluoroalkenylphosphonates

Aleksandr Anatol'evich Kadyrov 1
Aleksandr Anatol'evich Kadyrov
, 
Evgenii Maksovich Rokhlin 1
Evgenii Maksovich Rokhlin
1 A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
Published 30 November 1987
Communication , Volume 57, Issue 9, 852-863
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Kadyrov A. A., Rokhlin E. M. Fluoroalkenylphosphonates // Russian Chemical Reviews. 1988. Vol. 57. No. 9. pp. 852-863.
GOST all authors (up to 50)
Kadyrov A. A., Rokhlin E. M. Fluoroalkenylphosphonates // Russian Chemical Reviews. 1988. Vol. 57. No. 9. pp. 852-863.
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TY - JOUR
DO - 10.1070/RC1988v057n09ABEH003395
UR - https://rcr.colab.ws/publications/10.1070/RC1988v057n09ABEH003395
TI - Fluoroalkenylphosphonates
T2 - Russian Chemical Reviews
AU - Kadyrov, Aleksandr Anatol'evich
AU - Rokhlin, Evgenii Maksovich
PY - 1988
DA - 1987/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 852-863
IS - 9
VL - 57
ER -
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@article{1988_Kadyrov,
author = {Aleksandr Anatol'evich Kadyrov and Evgenii Maksovich Rokhlin},
title = {Fluoroalkenylphosphonates},
journal = {Russian Chemical Reviews},
year = {1988},
volume = {57},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1988v057n09ABEH003395},
number = {9},
pages = {852--863},
doi = {10.1070/RC1988v057n09ABEH003395}
}
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Kadyrov, Aleksandr Anatol'evich, and Evgenii Maksovich Rokhlin. “Fluoroalkenylphosphonates.” Russian Chemical Reviews, vol. 57, no. 9, Nov. 1988, pp. 852-863. https://rcr.colab.ws/publications/10.1070/RC1988v057n09ABEH003395.
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Abstract

In this review we survey the methods for the preparation of derivatives of fluoroalkenylphosphonic acid and their reactions. The main methods for obtaining these compounds are based on the reactions of fluoroolefins with phosphites and also on the elimination of halogens, hydrogen halides and alkyl halides from fluoroalkylphosphonates or fluorine-containing phosphorus ylides. The chemical properties of fluoroalkenylphosphonates are due to the combined effect of the fluorine atoms and the phosphonate group. Their reactions with different reagents leads to modifications of the phosphonate group, addition to the C=C bond, replacement of the vinyl halogen atom, and cleavage of the C–P bond.
The bibliography includes 96 references.