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Chem Commun (Camb) ; 52(2): 319-22, 2016 Jan 07.
Article in English | MEDLINE | ID: mdl-26515104

ABSTRACT

[5]Catenanes were synthesized by olefin metathesis dimerization. The reaction of pseudorotaxanes, which were derived from a [2]catenane and one equivalent of an ammonium salt bearing two terminal olefins in dichloromethane, with a catalytic amount of Grubbs catalyst afforded linear [5]catenanes in 12% yield. Intermolecular and intramolecular olefin metathesis reactions were controlled by the length of the alkyl chain of the ammonium salts.


Subject(s)
Alkenes/chemistry , Ammonium Compounds/chemistry , Catenanes/chemical synthesis , Rotaxanes/chemistry , Catalysis , Dimerization , Molecular Structure , Proton Magnetic Resonance Spectroscopy
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