Highly distorted Cone calix[4]arenes through intramolecular mc murry coupling reaction
- 1 July 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (29) , 7951-7958
- https://doi.org/10.1016/0040-4020(95)00411-z
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Calix[4]arenes Blocked in a Rigid Cone Conformation by Selective Functionalization at the Lower RimThe Journal of Organic Chemistry, 1995
- Direct Regioselective Formylation of Tetraalkoxycalix[4]arenes Fixed in the Cone Conformation and Synthesis of New CavitandsThe Journal of Organic Chemistry, 1995
- Gas-phase complexation of neutral molecules by upper rim bridged calix[4]arenesTetrahedron, 1995
- Urea-Derivatized p-tert-Butylcalix[4]arenes: Neutral Ligands for Selective Anion ComplexationThe Journal of Organic Chemistry, 1994
- NMR spectroscopic and X-ray crystallographic studies of calix[4]arene·Ag+complexes. Influence of bound Ag+on C2v–C2vinterconversion in cone-calix[4]arenesJournal of the Chemical Society, Perkin Transactions 2, 1994
- Computational studies of calix[4]arene homologs: influence of 5,11,17,23- and 25,26,27,28-substituents on the relative stability of four conformersTetrahedron, 1993
- Computational study of the structural, energetic, and acid-base properties of calix[4]arenesJournal of the American Chemical Society, 1990
- Carbonyl-coupling reactions using low-valent titaniumChemical Reviews, 1989
- The Application of Low-Valent Titanium Reagents in Organic SynthesisSynthesis, 1989
- New reagents for the intermolecular and intramolecular pinacolic coupling of ketones and aldehydesThe Journal of Organic Chemistry, 1976