Title of article
Alkylindan synthesis via an intermolecular [3+2] cycloaddition between unactivated alkenes and in situ generated p-quinomethanes
Author/Authors
Kim، نويسنده , , Shokaku and Kitano، نويسنده , , Yoshikazu and Tada، نويسنده , , Masahiro and Chiba، نويسنده , , Kazuhiro، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
5
From page
7079
To page
7083
Abstract
Alkylindans were synthesized by the intermolecular [3+2] cycloaddition of in situ generated p-quinomethanes and aliphatic alkenes. In a highly concentrated lithium perchlorate in nitromethane, p-quinomethanes were generated by DDQ oxidation of corresponding alkylphenols, and the desired cycloaddition reaction was completed efficiently to give various indans.
Keywords
Phenols , indanes/hydrindane , cyclization , addition reactions
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1638821
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