Synthesis of a novel 1,4-bridged calix[8]arene “Host” cavity
✍ Scribed by Youla S. Tsantrizos; Warren Chew; Lawrence D. Colebrook; Françoise Sauriol
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 273 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Two calix [4]arene cyclopeptides were synthesized by reacting 1,3-di(chlorocarbonyi-methoxy)-p-tert-butylca|ix[4]arene with cystine dimethyl ester dihydrochioride. One of them was found to be a good receptor for phosphomonoester.
## Synthesis and Conformational Analysis of Extended Calix[4]arenes and a Doubly Bridged arene. --(JOERGENSEN, M.;
New methods to obtain 1,2-bridged calix[4]arene-biscrowns in the 1,2-alternate conformation are described. The stereochemistry of the proximal double functionalization reaction is mainly governed by the solvent, the length of the polyether units and the base used to deprotonate the calix[4]arene.