ChemInform Abstract: Asymmetric Synthesis of Amino Acids by Catalytic Reduction of Azlactones of Substituted Acylaminoacrylic Acids. Part 23. Reductive Aminolysis of 2‐Methyl‐4‐benzylidene‐δ2‐oxazolin‐5‐one (I) with the Chiral Catalytic System Pd/(S)‐Amino Alcohol, e.g. PdCl2/(S)‐(II).

G V Chel'Tsova,E I Karpeiskaya,E I Klabunovskii

doi:10.1002/chin.198948291

ChemInform Abstract: Asymmetric Synthesis of Amino Acids by Catalytic Reduction of Azlactones of Substituted Acylaminoacrylic Acids. Part 23. Reductive Aminolysis of 2‐Methyl‐4‐benzylidene‐δ2‐oxazolin‐5‐one (I) with the Chiral Catalytic System Pd/(S)‐Amino Alcohol, e.g. PdCl2/(S)‐(II).

G V Chel'Tsova, E I Karpeiskaya + Show 1 more

https://doi.org/10.1002/chin.198948291

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Journal: ChemInform

Publication Date: Nov 28, 1989

Affiliation: Eskom (South Africa)

#Asymmetric Synthesis Of Amino Acids #Amino Alcohol + Show 8 more

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ChemInform Abstract: Asymmetric Synthesis of Amino Acids by Catalytic Reduction of Azlactones of Substituted Acylaminoacrylic Acids. Part 23. Reductive Aminolysis of 2‐Methyl‐4‐benzylidene‐δ2‐oxazolin‐5‐one (I) with the Chiral Catalytic System Pd/(S)‐Amino Alcohol, e.g. PdCl2/(S)‐(II).

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