Strecker synthesis

A method for synthesizing amino acids from aldehydes or ketones, ammonia, and a cyanide source.

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Sc(BINOL)₂Li: A new heterobimetallic catalyst for the asymmetric Strecker reaction
Related Chemicals
- α-<(phenylmethyl)amino>-2-naphthalenacetonitrile
- Benzaldehyde
- Cyclohexane
Synthesis of γ-oxo α-amino acids from L-aspartic acid
Related Chemicals
- 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)-
General synthesis of enantiomerically pure β-amino acids
Related Chemicals
- (S)-2-N,N-dibenzylamino-3-cyanopropanoic acid benzyl ester
α-Phenylglycinol as chiral auxiliary in diastereoselective Strecker synthesis of α-amino acids
Related Chemicals
- methyl (E)-2-(benzylideneamino)-2-phenylacetate

Characterization Chiral Heterobimetallic complex Sc(BINOL)2Li Catalyst Enantioselective Addition Cyanide source Imines Hydrolysis Diastereoselective Asymmetric catalysis Work-Up Organocatalysis Chiral Auxiliary Approach Chirality transfer Transition Metal-Catalyzed Reactions Oxidative Cleavage Chiral Auxiliary Enzymatic Resolution Scandium (Sc) BINOL (1,1'-Bi-2-naphthol) Li (Lithium) Chiral Pool Approach Resolution Techniques Stereocontrolled Functionalization α-Phenylglycinol

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