Stereoselective Conjugate Additions of Hydrazines, Oximes, and Hydroxylamines to α,β-Unsaturated Imides
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Elsevier
Reference30 articles.
1. Enantioselective Synthesis of β-Amino Acids: TMS-SAMP as a Chiral Ammonia Equivalent for the Aza Analogous Michael Addition to α,β-Unsaturated Esters;Enders;Angew. Chem., Int. Ed. Engl.,1995
2. Diastereo- and Enantioselective Synthesis of Carbocyclic and Heterocyclic β-Amino Acids by Tandem Aza Michael Addition/Intramolecular Cyclization;Enders;Liebigs Ann./Rec.,1997
3. One Step Synthesis of Optically Active Diazabicyclo[3.3.0]octanones or Diazabicyclo[4.3.0]nonanones by Asymmetric Conjugate Addition of Cyclic Hydrazine;Seki;Heterocycles,2012
4. Enantioselective Conjugate Addition of Hydrazines to α,β-Unsaturated Imides. Synthesis of Chiral Pyrazolidinones;Sibi;J. Am. Chem. Soc.,2007
5. Enantioselective Conjugate Additions of Aldoximes to 3-Crotonoyl-2-oxazolidinone and 1-Crotonoyl-3-phenyl-2-imidazolidinone Catalyzed by the Aqua Complex Between R, R-DBFOX/Ph and Zinc(II) Perchlorate;Nakama;Tetrahedron Lett.,2002
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