Title of article
A Regioselective Route to 5- and 6-Azaindoles
Author/Authors
Lomberget، Thierry نويسنده , , Radix، Sylvie نويسنده , , Barret، Roland نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
-207
From page
208
To page
0
Abstract
The synthesis of 4,7-dimethoxy 5- and 6-azaindoles, a structural unit that is present in recently developed anti-HIV-1 agents, was achieved in a regioselective manner. The developed strategy is based on the appropriate choice of a protecting group during a lithium-mediated formylation step, followed by thermal cyclization of azidoacrylates.
Keywords
pyridines , Metalations , 5- and 6-azaindoles , Azides , regioselectivity
Journal title
Synlett
Serial Year
2005
Journal title
Synlett
Record number
110744
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