Novel Upper Rim Functionalizations of Calix[4]arenes using the Tscherniac-Einhorn Amidomethylation Reaction
β Scribed by Kjeld J.C. van Bommel; Folke Westerhof; Willem Verboom; David N. Reinhoudt; Ron Hulst
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 147 KB
- Volume
- 341
- Category
- Article
- ISSN
- 1615-4150
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β¦ Synopsis
A variety of novel upper rim functionalized calix-[4]arenes have been synthesized, using the Tscherniac-Einhorn amidomethylation reaction. Partially or fully alkylated calix [4]arenes bearing propyl or ethoxyethyl substituents could be easily condensed with various N-methylol-amides and -imides under mild conditions. The resulting methyl-1
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Synthetic routes were developed to link L-alanine methyl ester or L-alanyl-L-alanine methyl ester at the upper rim of calix [4]arenes blocked in the cone conformation. Several tetra-(3 and 6) and difunctionalized (11 and 12) amino acids containing macrocycles were obtained. Reaction of these compoun