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Mendeleev Communications, 1992, Volume 2, Issue 3, Pages 106–108
DOI: https://doi.org/10.1070/MC1992v002n03ABEH000157
(Mi mendc5428)
 

This article is cited in 20 scientific papers (total in 20 papers)

Phosphorylated Resorcinol-based Cyclophanes

L. N. Markovsky, V. I. Kalchenko, D. M. Rudkevich, A. N. Shivanyuk

Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, Ukraine
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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Document Type: Article
Language: English


Citation: L. N. Markovsky, V. I. Kalchenko, D. M. Rudkevich, A. N. Shivanyuk, “Phosphorylated Resorcinol-based Cyclophanes”, Mendeleev Commun., 2:3 (1992), 106–108
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  • This publication is cited in the following 20 articles:
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