Title of article :
Silyl-enolization-asymmetric Claisen rearrangement of 2-allyloxyindolin-3-one: enantioselective total synthesis of 3a-hydroxypyrrolo[2,3-b]indoline alkaloid alline
Author/Authors :
Kawasaki، نويسنده , , Tomomi and Takamiya، نويسنده , , Wataru and Okamoto، نويسنده , , Naoki and Nagaoka، نويسنده , , Miyuki and Hirayama، نويسنده , , Tetsuya، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2006
Pages :
4
From page :
5379
To page :
5382
Abstract :
Asymmetric Claisen rearrangement triggered by silyl-enolization of 2-(1′-nonel-3′-yloxy)indolin-3-ones was performed in order to prepare 3-(2′-nonenyl)-3-hydroxyindolin-2-ones. Total synthesis of 3-hydroxypyrrolo[2,3-b]indoline alkaloid, (+)-alline was achieved by transformation of the allylic moiety of 3-(2′-nonenyl)-3-hydroxyindolin-2-one to amine followed by reductive cyclization.
Journal title :
Tetrahedron Letters
Serial Year :
2006
Journal title :
Tetrahedron Letters
Record number :
1851500
Link To Document :
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