N,N-Diisopropyl-N-phosphonyl Imines Lead to Efficient Asymmetric Synthesis of Aziridine-2-Carboxylic Esters

Similar Items

• Chiral N-Phosphonyl Imine Chemistry: Asymmetric Additions of Ester Enolates for the Synthesis of β-Amino Acids
  od: Han, Jianlin, i dr.
  Izdano: (2008)
• Asymmetric Synthesis of α-Amino 1,3-Dithianes via Chiral N-Phosphonyl Imine-based Umpolung Reaction
  od: Kattamuri, Padmanabha V., i dr.
  Izdano: (2011)
• Asymmetric Hydrophosphylation of Chiral N-Phosphonyl Imines Provides an Efficient Approach to Chiral α-Amino Phosphonates
  od: Kaur, Parminder, i dr.
  Izdano: (2010)
• Asymmetric synthesis of α-alkenyl homoallylic primary amines via 1,2-addition of Grignard reagent to α,β-unsaturated phosphonyl imines
  od: Xiong, Yiwen, i dr.
  Izdano: (2013)
• Asymmetric Carbamoyl Anion Additions to Chiral N-Phosphonyl Imines via the GAP Chemistry Process and Stereoselectivity Enrichments
  od: Seifert, Cole W., i dr.
  Izdano: (2014)