Title of article
Lithium Acetate-catalyzed Michael Reaction between Trimethylsilyl Enolate and (alpha),(beta)-Unsaturated Carbonyl Compound
Author/Authors
Mukaiyama، Teruaki نويسنده , , Nakagawa، Takashi نويسنده , , Fujisawa، Hidehiko نويسنده , , Nagata، Yuzo نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
-1015
From page
1016
To page
0
Abstract
Lithium acetate-catalyzed Michael reaction between trimethylsilyl enolates and (alpha),(beta)-unsaturated carbonyl compounds in DMF proceeded smoothly to afford the corresponding Michael-adducts in good to high yields. Hindered (alpha),(beta)-unsaturated ketones also behaved as an excellent Michael-acceptor in the above reaction at room temperature.
Keywords
grinding , Surface finish , Genetic-fuzzy system , prediction , Power requirement , Application-production research
Journal title
CHEMISTRY LETTERS
Serial Year
2004
Journal title
CHEMISTRY LETTERS
Record number
28671
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