Title of article
Extending Pummerer reaction chemistry. Examination of the prospects for forming vicinal quaternary carbon centers
Author/Authors
Feldman، نويسنده , , Ken S. and Nuriye، نويسنده , , Ahmed Yimam، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2009
Pages
3
From page
1914
To page
1916
Abstract
Pummerer chemistry applied to 2-sulfinyl indoles promotes oxidative cyclization of pendant nucleophiles to furnish C(3) spirocyclic indolenine products. Use of tetrasubstituted silyl enol ether nucleophiles in this transform yields spirocycles featuring vicinal all-carbon quaternary centers in two cases, but fails when a nearby amine can intervene.
Journal title
Tetrahedron Letters
Serial Year
2009
Journal title
Tetrahedron Letters
Record number
1863286
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