A HighlySyn-selective Michael Reaction of Enamines with α,β-Unsaturated EstersviaCationic Intermediates
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/18/6/18_6_943/_pdf
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1. Michael Addition of Ketone Enolates to α,β-Unsaturated Esters or Amides in a One-Pot Procedure: Highly Efficient Effect of Lithium Salt Generated in situ on Organotin Enolate;Synthesis;2005
2. Michael Addition of Stannyl Ketone Enolate to α,β-Unsaturated Esters Catalyzed by Tetrabutylammonium Bromide and an ab Initio Theoretical Study of the Reaction Course;Journal of the American Chemical Society;2003-05-23
3. 1-Pyrrolidino-1-cyclohexene;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. Novel Reaction System Using Highly Coordinated Organotin Enolates.;Journal of Synthetic Organic Chemistry, Japan;2001
5. The First Michael Addition of Metal Ketone Enolates to α,β-Unsaturated Esters under Catalytic Conditions: Tin Enolate with a Catalytic Amount of Tetrabutylammonium Bromide;The Journal of Organic Chemistry;1999-03-13
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