Title of article :
A direct entry to the 1-methoxyindole skeleton and to the corresponding indoles by a novel rearrangement: general syntheses of substituted 1-methoxyindoles
Author/Authors :
Selvakumar، نويسنده , , N and Reddy، نويسنده , , B.Yadi and Azhagan، نويسنده , , A.Malar and Khera، نويسنده , , Manoj Kumar and Babu، نويسنده , , J.Moses and Iqbal، نويسنده , , Javed، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
5
From page :
7065
To page :
7069
Abstract :
A short and efficient route to 1-methoxyindoles via a novel rearrangement is disclosed. This route involves only three steps from commercially available nitro compounds. The methodology is also generalized with a variety of examples to afford a series of 2-substituted-1-methoxyindoles possessing an electron-withdrawing group at position 3. In addition, a 1-methoxyindole compound 10 was converted to the corresponding indole 11 under mild conditions thereby constituting a new synthesis of substituted indoles.
Keywords :
Decarboxylation , Rearrangement , alkaloid , Alkylation , nucleophilic catalysis
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1654569
Link To Document :
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