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Org Lett ; 11(10): 2189-92, 2009 May 21.
Article in English | MEDLINE | ID: mdl-19371074

ABSTRACT

Bicyclic diazenium salts were efficiently prepared by a Lewis acid mediated intramolecular cycloaddition. Terminal olefins provided mixtures of fused and bridged bicyclic diazenium salts. The alpha-chloroazo cycloaddition precursors were conveniently prepared from the corresponding phenyl hydrazones by treatment with chlorodimethylsulfonium chloride.


Subject(s)
Alkenes/chemical synthesis , Azo Compounds/chemical synthesis , Bridged Bicyclo Compounds/chemical synthesis , Alkenes/chemistry , Azo Compounds/chemistry , Bridged Bicyclo Compounds/chemistry , Combinatorial Chemistry Techniques , Cyclization , Models, Molecular , Molecular Structure , Salts
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