## Abstract Bowlβshaped chiral homotriazacalixarenes were prepared by the cyclization reactions of chiral triamines with three equimolar amounts of bis(chloromethyl) phenols or bis(chloromethyl) phenolβformaldehyde dimers in moderate yields. The corresponding acyclic phenolβformaldehyde oligomers w
Synthesis and Properties of Bowl-Shaped Homotriazacalix[3 and 6]arenes and the Acyclic Analogues.
β Scribed by Kazuaki Ito; Tomokazu Sato; Yoshihiro Ohba
- Book ID
- 101946186
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 4 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Three oligomers of ethylene-bridged 3,6-fluorene were synthesized starting from phenanthrenequinone. McMurry reaction was applied to synthesize the cyclic compound. Horner-Emmons reaction was used to synthesize the linear compounds with all-trans configuration. The crystal structure of the cyclic c
1,3-Dithiole-[3]-and [4]-dendralenes (2 and 3) have successfully been synthesized by using Vilsmeyer reactions on 2,2'-(ethanediylidene)bis(l,3-dithiole) (5) and 2 and the following Wittig reaction, Their electrochemical properties are discussed in comparison with those of 2 and 1,3-dithioleI4lradia