Title of article :
Reversal of the regioselectivity in a cycloaddition of o-quinones by varying the position of alkoxy substituents
Author/Authors :
Kuboki، نويسنده , , Atsuhito and Yamamoto، نويسنده , , Toru and Taira، نويسنده , , Mamie and Arishige، نويسنده , , Tetsuya and Konishi، نويسنده , , Rina and Hamabata، نويسنده , , Mami and Shirahama، نويسنده , , Mutsumi and Hiramatsu، نويسنده , , Takeya and Kuyama، نويسنده , , Kohei and Ohira، نويسنده , , Susumu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2008
Pages :
4
From page :
2558
To page :
2561
Abstract :
We have investigated the regioselective cycloaddition of o-quinones 1b–e with the protected sinapyl alcohol 2. It was found that the position of the alkoxy substituent on the o-quinone ring controlled the regioselectivity of the cycloaddition. In addition, our reported procedure for determining the location of the side chains on 1,4-benzodioxanes has been improved.
Keywords :
1 , o-quinone , 4-benzodioxane , cycloaddition , regioselectivity
Journal title :
Tetrahedron Letters
Serial Year :
2008
Journal title :
Tetrahedron Letters
Record number :
1858915
Link To Document :
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