Title of article :
Gold-catalyzed reactivity of 3-silyloxy-1,5-enynes: a synthetic tool for the synthesis of complex structures and its limitations
Author/Authors :
Helge Menz، نويسنده , , J?rg T. Binder، نويسنده , , Benedikt Crone، نويسنده , , Alexander Duschek، نويسنده , , Timm T. Haug، نويسنده , , Stefan F. Kirsch، نويسنده , , Philipp Klahn، نويسنده , , Clémence Liébert، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
9
From page :
1880
To page :
1888
Abstract :
Gold-catalyzed reactions of 3-silyloxy-1,5-enynes in the presence of sterically demanding alcohols afford 4-acylcyclopentenes. The cascade process most likely proceeds through a 6-endo-dig carbocyclization and subsequent pinacol-type rearrangement. Studies that define scope and limitations of the cyclization–migration strategy are also described. An alternative cascade yields highly substituted aryls through an unprecedented cyclization–fragmentation pathway.
Journal title :
Tetrahedron
Serial Year :
2009
Journal title :
Tetrahedron
Record number :
1095159
Link To Document :
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