z-logo
Premium
Synthesis of p‐tert ‐Butylcalix[10]crowns
Author(s) -
ZHAN JunYan,
LI HaiBing,
HUANG ShaoWei
Publication year - 2008
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.200890230
Subject(s) - chemistry , crown (dentistry) , polyethylene glycol , calixarene , toluene , ethylene glycol , polymer chemistry , acetone , medicinal chemistry , organic chemistry , molecule , materials science , composite material
A series of calix[10]crowns were synthesized for the first time. By reacting p‐tert ‐butylcalix[10]arene with ethylene glycol ditosylate or polyethylene glycol ditosylates in a system of K 2 CO 3 /toluene or Cs 2 CO 3 /acetone, a series of calix[10]crowns such as 1,2‐calix[10]crown‐4, 1,3‐calix[10]crown‐2, 1,2‐calix[10]crown‐3, 1,3‐calix[10]crown‐3, 1,4‐calix[10]crown‐4 and 1,6‐calix[10]crown‐4 were obtained.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom