Stereoselection in the Synthesis of threo‐ and erythro‐3‐Amino‐2‐hydroxy‐4‐phenylbutanoic Acid Using Chiral Acetal Templates.

@article{Herranz1989StereoselectionIT,
  title={Stereoselection in the Synthesis of threo‐ and erythro‐3‐Amino‐2‐hydroxy‐4‐phenylbutanoic Acid Using Chiral Acetal Templates.},
  author={Rosario Herranz and Julia Castro‐Pichel and Soledad Vinuesa and T. Garcia‐Lopez},
  journal={ChemInform},
  year={1989},
  volume={20}
}
1 Citations
Aminopeptidase‐N/CD13 (EC 3.4.11.2) inhibitors: Chemistry, biological evaluations, and therapeutic prospects
TLDR
An update on the biological and pharmacological profiles of known natural and synthetic APN inhibitors and current status on their potential use as therapeutic agents is discussed with regard to toxicity and specificity.

References

Stereoselection in the synthesis of threo- and erythro-3-amino-2-hydroxy-4-phenyl-butanoic acid using chiral acetal templates
Boron trifluoride-diethyl ether mediated addition of trimethylsilylcyanide (TMSCN) to the chiral acetals derived from Z-L- and Z-D-phenyl alaninal, (Z=N-benzyloxycarbonyl), and (+)-(2S,4S)- and