Cyclocondensation of 2-Methylresorcinol with Formaldehyde. A Synthesis of Conformationally Mobile Metacyclophanes
- 1 October 1989
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 18 (10) , 1815-1816
- https://doi.org/10.1246/cl.1989.1815
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Host-guest complexation. 48. Octol building blocks for cavitands and carcerandsThe Journal of Organic Chemistry, 1989
- Structurally new macrocycles from the resorcinol-aldehyde condensation. Configurational and conformational analyses by means of dynamic NMR, NOE, and T1 experimentsThe Journal of Organic Chemistry, 1988
- New hydrophobic host molecules containing multiple redox-active centresTetrahedron Letters, 1988
- Polar host-guest interaction. Binding of nonionic polar compounds with a resorcinol-aldehyde cyclooligomer as a lipophilic polar hostJournal of the American Chemical Society, 1988
- A Macrobicyclic Polyphenoxide as Receptor Analogue for Choline and Related Ammonium CompoundsAngewandte Chemie International Edition in English, 1986
- Calixarenes. 13. The conformational properties of calix[4]arenes, calix[6]arenes, calix[8]arenes, and oxacalixarenesJournal of the American Chemical Society, 1985
- Two stereoisomeric macrocyclic resorcinol-acetaldehyde condensation productsThe Journal of Organic Chemistry, 1980
- Cyclooligomeric phenol-aldehyde condensation products. 2. Stereoselective synthesis and DNMR study of two 1,8,15,22-tetraphenyl[14]metacyclophan-3,5,10,12,17,19,24,26-octolsJournal of the American Chemical Society, 1980