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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 1
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Original Articles

Regioselective C-3 Alkylations of Oxindole Dianion

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Pages 1-10 | Published online: 03 Jan 2007
 

Abstract

Oxindole is converted to its dianion by treatment with two equivalents each of n-BuLi and TMEDA. Alkylations with a number of common electrophiles define the scope of synthetically useful transformations leading to 3-monosubstituted and 3,3-disubstituted oxindoles.

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