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J Org Chem ; 67(5): 1705-7, 2002 Mar 08.
Article in English | MEDLINE | ID: mdl-11871910

ABSTRACT

Stereochemically well-defined homoallylic thioethers 3 are synthesized via Lewis acid promoted condensation reaction between chiral organosilane reagents 2 and in situ generated thionium ions. The stereochemical course of the reaction is consistent with earlier reports concerning crotylsilations of oxonium ions.


Subject(s)
Ethers/chemical synthesis , Quaternary Ammonium Compounds/chemistry , Silanes/chemistry , Acetals/chemistry , Alkanes/chemistry , Butanols/chemistry , Catalysis , Chemistry, Organic/methods , Ethers/chemistry , Ketones/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Stereoisomerism , Sulfur/chemistry , Tin Compounds/chemistry
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