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Phosphorylated Resorcinol-based Cyclophanes

Leonid Nikolaevich Markovsky 1
Leonid Nikolaevich Markovsky
, 
Vitaliy Ivanovich Kalchenko 1
Vitaliy Ivanovich Kalchenko
, 
Dmitrii Mar'yanovich Rudkevich 1
Dmitrii Mar'yanovich Rudkevich
, 
Aleksandr Nikolaevich Shivanyuk 1
Aleksandr Nikolaevich Shivanyuk
1 Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, Ukraine
10.1070/MC1992v002n03ABEH000157
Published 1992-09-30
Communication , Volume 2, Issue 3, 106-108
17
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Markovsky L. N. et al. Phosphorylated Resorcinol-based Cyclophanes // Mendeleev Communications. 1992. Vol. 2. No. 3. pp. 106-108.
GOST all authors (up to 50) Copy
Markovsky L. N., Kalchenko V. I., Rudkevich D. M., Shivanyuk A. N. Phosphorylated Resorcinol-based Cyclophanes // Mendeleev Communications. 1992. Vol. 2. No. 3. pp. 106-108.
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TY - JOUR
DO - 10.1070/MC1992v002n03ABEH000157
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000157
TI - Phosphorylated Resorcinol-based Cyclophanes
T2 - Mendeleev Communications
AU - Markovsky, Leonid Nikolaevich
AU - Kalchenko, Vitaliy Ivanovich
AU - Rudkevich, Dmitrii Mar'yanovich
AU - Shivanyuk, Aleksandr Nikolaevich
PY - 1992
DA - 1992/09/30
PB - Mendeleev Communications
SP - 106-108
IS - 3
VL - 2
ER -
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@article{1992_Markovsky,
author = {Leonid Nikolaevich Markovsky and Vitaliy Ivanovich Kalchenko and Dmitrii Mar'yanovich Rudkevich and Aleksandr Nikolaevich Shivanyuk},
title = {Phosphorylated Resorcinol-based Cyclophanes},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000157},
number = {3},
pages = {106--108},
doi = {10.1070/MC1992v002n03ABEH000157}
}
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Markovsky, Leonid Nikolaevich, et al. “Phosphorylated Resorcinol-based Cyclophanes.” Mendeleev Communications, vol. 2, no. 3, Sep. 1992, pp. 106-108. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000157.

Abstract

Complete and partial O-functionalization of the octahydroxytetramethyl[14]metacyclophane with phosphoryl groups has been carried out, arid reversible intramolecular addition of hydroxy or trimethylsilyloxy groups to the neighbouring P=O bonds with the formation of spirophosphorane fragments has been shown to be typical of the 3,10,17,24-tetrahydroxy(tetrakistrimethylsilbxy)-5,12,19,26-tetrakis-o-phenylenephosphoryloxy-1,8,15,22-tetramethyl [14]metacyclophane.

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