Inherently chiral calix[4]arenes with asymmetrical superposition of substituents at the lower and the upper rims of macrocycle
β Scribed by Myroslav O Vysotsky; Maxym O Tairov; Vladimir V Pirozhenko; Vitaly I Kalchenko
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 212 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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## 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
A comparative study on a series of penta-O-alkylated p-H-calix[5]arenes lb-e and p-tertbutylcalix[5]arenes lg-m shows that the former are inherently mobile and adopt in solution non-cone conformations. The 1,2-alternate conformation for penta-O-benzyl ether lc was proven by single-crystal X-ray anal