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J Org Chem ; 76(20): 8347-54, 2011 Oct 21.
Article in English | MEDLINE | ID: mdl-21882812

ABSTRACT

In the presence of copper(I) iodide, heteroaromatic ß-iodo-α,ß-unsaturated carboxylic acid systems opposed to terminal alkyne afford selectively 6-endo-dig cyclization products via a tandem coupling oxacyclization reaction.


Subject(s)
Chemistry, Pharmaceutical/methods , Indoles/chemical synthesis , Pyrans/chemical synthesis , Thiophenes/chemical synthesis , Alkynes/chemistry , Carboxylic Acids/chemistry , Catalysis , Copper/chemistry , Cyclization , Iodides/chemistry , Magnetic Resonance Spectroscopy , Stereoisomerism
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