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Synthesis of Substituted Crown-Ethers by radical addition of 18-crown-6

✍ Scribed by Ju. B. Zeleconok; V. V. Orlovskij; Prof. Dr. S. S. Zlotskij; Prof. Dr. D. L. Rachmankulov


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
238 KB
Volume
332
Category
Article
ISSN
1615-4150

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✦ Synopsis


Abstract

An example of the synthesis of substituted crown‐ethers by radical addition reaction of 18‐crown‐6 (1) to several α‐olefins (2a‐e), cyclohexene (2f), vinyl butyl ether (2g), allyl alcohol (2h), trimethylvinylsilane (2i), diethylmaleate (2j) and formaldehyde (2k) in the presence of a peroxide initiator was studied.

The dependence of the yield of the addition product upon reaction conditions was also investigated.


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## Abstract The synthesis and characterization of novel Schiff base liquid crystalline crown ethers prepared from the intermediates 4‐(4′‐alkoxylbiphenyl‐4‐carbonyl) benzaldehyde, __cis‐__ and __trans__‐4,4′‐diaminodibenzo‐18‐crown‐6 are described. The structure of these compounds have been well ch