Аннотация:
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.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
L. N. Markovsky, V. I. Kalchenko, D. M. Rudkevich, A. N. Shivanyuk, “Phosphorylated Resorcinol-based Cyclophanes”, Mendeleev Commun., 2:3 (1992), 106–108
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5428
https://www.mathnet.ru/rus/mendc/v2/i3/p106
Эта публикация цитируется в следующих 19 статьяx:
Pawan Kumar, V. B. Raja Mani Kandan, Prabukumar Balakrishnan, P. K. Sudhadevi Antharjanam, Venkatakrishnan Parthasarathy, “Leveraging Torsional and Steric Strains: A Pre‐macrocyclization Strategy Enables Conformation‐Specific Fullerene Binding in m‐Cyclophanes”, Angewandte Chemie, 135:41 (2023)
Pawan Kumar, V. B. Raja Mani Kandan, Prabukumar Balakrishnan, P. K. Sudhadevi Antharjanam, Venkatakrishnan Parthasarathy, “Leveraging Torsional and Steric Strains: A Pre‐macrocyclization Strategy Enables Conformation‐Specific Fullerene Binding in m‐Cyclophanes”, Angew Chem Int Ed, 62:41 (2023)
Jordan N. Smith, Thomasin K. Brind, Simon B. Petrie, Mikaela S. Grant, Nigel T. Lucas, “One-Step Synthesis of C2v-Symmetric Resorcin[4]arene Tetraethers”, J. Org. Chem., 85:6 (2020), 4574
Anthony Wishard, Bruce C. Gibb, Calixarenes and Beyond, 2016, 195
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