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Acyclic Alkoxy- and Aryloxy-phosphoranes

Leonid Nikolaevich Markovskii 1
Leonid Nikolaevich Markovskii
, 
Natal'ya Petrovna Kolesnik 1
Natal'ya Petrovna Kolesnik
, 
Yuriy Grigorievich Shermolovich 1
Yuriy Grigorievich Shermolovich
1 Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, Kyiv
10.1070/RC1987v056n09ABEH003312
Published 30 November 1986
Communication , Volume 56, Issue 9, 894-905
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Markovskii L. N., Kolesnik N. P., Shermolovich Y. G. Acyclic Alkoxy- and Aryloxy-phosphoranes // Russian Chemical Reviews. 1987. Vol. 56. No. 9. pp. 894-905.
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Markovskii L. N., Kolesnik N. P., Shermolovich Y. G. Acyclic Alkoxy- and Aryloxy-phosphoranes // Russian Chemical Reviews. 1987. Vol. 56. No. 9. pp. 894-905.
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TY - JOUR
DO - 10.1070/RC1987v056n09ABEH003312
UR - https://rcr.colab.ws/publications/10.1070/RC1987v056n09ABEH003312
TI - Acyclic Alkoxy- and Aryloxy-phosphoranes
T2 - Russian Chemical Reviews
AU - Markovskii, Leonid Nikolaevich
AU - Kolesnik, Natal'ya Petrovna
AU - Shermolovich, Yuriy Grigorievich
PY - 1987
DA - 1986/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 894-905
IS - 9
VL - 56
ER -
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@article{1987_Markovskii,
author = {Leonid Nikolaevich Markovskii and Natal'ya Petrovna Kolesnik and Yuriy Grigorievich Shermolovich},
title = {Acyclic Alkoxy- and Aryloxy-phosphoranes},
journal = {Russian Chemical Reviews},
year = {1987},
volume = {56},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1987v056n09ABEH003312},
number = {9},
pages = {894--905},
doi = {10.1070/RC1987v056n09ABEH003312}
}
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Markovskii, Leonid Nikolaevich, et al. “Acyclic Alkoxy- and Aryloxy-phosphoranes.” Russian Chemical Reviews, vol. 56, no. 9, Nov. 1987, pp. 894-905. https://rcr.colab.ws/publications/10.1070/RC1987v056n09ABEH003312.
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Abstract

The review gives a systematic account of the methods of synthesis, physical properties, structure, and reactivity of pentacoordinate phosphorus compounds having an acyclic structure and containing alkoxy- and aryloxy-substituents.
The bibliography includes 91 references.