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Regioselective synthesis of calix[4]arene 1,3-di- and monosubstituted sulfur-containing Schiff bases
Authors:Jing Sun  Dong Mei Liu  Jin Xiang Wang  Chao Guo Yan
Affiliation:1. College of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou, 225002, China
Abstract:Regioselective alkylations of p-tert-butylcalix[4]arene with 3-methoxy-4-ω-chloroalkoxy-benzaldehydes in the system of K2CO3/KI/CH3CN efficiently produce 1,3-di- and monosubstituted aldehydes according to the length of alkyl chains in alkylating reagent, which provides a versatile protocol for preparing calixarene 1,3-di- and sulfur-containing Schiff bases.
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