Regioselective mannich reactions via trimethylsilyl enol ethers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Dimethyl(methylene)ammonium Iodide
2. Reactions of silyl enol ethers and lactone enolates with dimethyl(methylene)ammonium iodide. The bis-.alpha.-methylenation of pre-vernolepin and pre-vernomenin
3. New applications of the Mannich reaction. Use of dimethyl(methylene)ammonium trifluoroacetate for regiospecific carbanion quenching. A new route to .alpha.-methylene-.gamma.-butyrolactone
4. Addition of eschenmoser's salt to ketone, ester, & lactone enolates. A convenient synthesis of a-methylene carbonyls via mannich intermediates
5. A Convenient Tertiary Amine Synthesis. Use of Methylenedimethylammonium Trifluoroacetate
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