Title of article :
Cycloaddition studies directed toward the strychnos alkaloid minfiensine
Author/Authors :
Drew R. Bobeck، نويسنده , , Drew R. and France، نويسنده , , Stefan and Leverett، نويسنده , , Carolyn A. and Sلnchez-Cantalejo، نويسنده , , Fernando and Padwa، نويسنده , , Albert، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
3
From page :
3145
To page :
3147
Abstract :
The thermolysis of several imidofuranyl carbamates delivers products derived from an intramolecular [4+2]-cycloaddition reaction. In the case of the ortho-azido aryl carbamate 13, the preferred path proceeds by an electrocyclization of a nitrene intermediate to produce a 3-substituted indole. Attempts to reduce the azido group resulted in a novel intramolecular aza-Wittig reaction with the neighboring imido group.
Journal title :
Tetrahedron Letters
Serial Year :
2009
Journal title :
Tetrahedron Letters
Record number :
1864185
Link To Document :
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