Regioselective Nucleophilic Ring Opening Reactions of 2,2-Disubstituted Aziridines -The Asymmetric Synthesis of Ξ±,Ξ±-Disubstituted Amino Acids. -It is shown that, under appropriate conditions, 2,2disubstituted aziridines like (I) and (V) undergo regioselective ring opening reactions at C-3 with carb
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ChemInform Abstract: Regioselective Ring Opening of Malic Acid Anhydrides by Carbon Nucleophiles. Application in the Synthesis of Chiral Tetronic Acids.
β Scribed by Christos A. Mitsos; Alexandros L. Zografos; Olga Igglessi-Markopoulou
- Publisher
- John Wiley and Sons
- Year
- 2000
- Weight
- 28 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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