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Chiral hydroxy phosphonates: synthesis, configuration and biological properties

Oleg Ivanovich Kolodiazhnyi 1
Oleg Ivanovich Kolodiazhnyi
1 Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, Kyiv
Published 30 November 2005
Communication , Volume 75, Issue 3, 227-253
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Kolodiazhnyi O. I. Chiral hydroxy phosphonates: synthesis, configuration and biological properties // Russian Chemical Reviews. 2006. Vol. 75. No. 3. pp. 227-253.
GOST all authors (up to 50)
Kolodiazhnyi O. I. Chiral hydroxy phosphonates: synthesis, configuration and biological properties // Russian Chemical Reviews. 2006. Vol. 75. No. 3. pp. 227-253.
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TY - JOUR
DO - 10.1070/RC2006v075n03ABEH001193
UR - https://rcr.colab.ws/publications/10.1070/RC2006v075n03ABEH001193
TI - Chiral hydroxy phosphonates: synthesis, configuration and biological properties
T2 - Russian Chemical Reviews
AU - Kolodiazhnyi, Oleg Ivanovich
PY - 2006
DA - 2005/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 227-253
IS - 3
VL - 75
ER -
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@article{2006_Kolodiazhnyi,
author = {Oleg Ivanovich Kolodiazhnyi},
title = {Chiral hydroxy phosphonates: synthesis, configuration and biological properties},
journal = {Russian Chemical Reviews},
year = {2006},
volume = {75},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2006v075n03ABEH001193},
number = {3},
pages = {227--253},
doi = {10.1070/RC2006v075n03ABEH001193}
}
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Kolodiazhnyi, Oleg Ivanovich. “Chiral hydroxy phosphonates: synthesis, configuration and biological properties.” Russian Chemical Reviews, vol. 75, no. 3, Nov. 2006, pp. 227-253. https://rcr.colab.ws/publications/10.1070/RC2006v075n03ABEH001193.
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Abstract

Published data on the synthesis, absolute configurations and biological properties of chiral hydroxy phosphonates are generalised and described systematically. Examples of asymmetric synthesis of hydroxy phosphonates by the phospho-aldol reaction, reduction of keto phosphonates, chemo-enzymatic approach, and so on are discussed. Methods for determination of the optical purity and absolute configuration of hydroxy phosphonates using modification by chiral reagents, NMR, circular dichroism, GLC and HPLC on columns with chiral sorbents are considered. The significance of hydroxy phosphonates as promising compounds for the development of new drugs and bioregulators is demonstrated.