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