Title of article :
Cycloisomerization of 1,6-enynes in organoaqueous medium: an efficient and eco-friendly access to furan derivatives. Synthesis of a key intermediate of podophyllotoxin
Author/Authors :
Jean-Christophe Galland، نويسنده , , Sonia Dias، نويسنده , , Monique Savignac، نويسنده , , Jean-Pierre Genêt، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
12
From page :
5137
To page :
5148
Abstract :
The first cycloisomerization of enynes catalyzed by Pd(TPPTS)3 catalyst in aqueous medium to give functionalized furans is described. This new reaction has been applied to the synthesis of podophyllotoxin analog.
Keywords :
organoaqueous medium , carbohydroxypalladation , enynes , Palladium , Podophyllotoxin
Journal title :
Tetrahedron
Serial Year :
2001
Journal title :
Tetrahedron
Record number :
1082110
Link To Document :
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