101669-82-3Relevant articles and documents
Ready access to stereodefined β-hydroxy-γ-amino acids. Enantioselective synthesis of fully protected cyclohexylstatine
Castejon, Patricia,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni
, p. 7063 - 7086 (2007/10/03)
A convenient entry to enantiopure syn or anti β-hydroxy-γ-amino acids is described. The starting compounds for the synthesis, anti 3-amino-1,2-diols, are readily available in high enantiomeric purity through catalytic asymmetric epoxidation of an allylic alcohol and titanium-promoted oxirane opening. After adequate protection of the nitrogen, a stereodivergent sequence leads to both anti and syn N-Boc aminoalkyl epoxides. Subsequent regioselective ring-opening with cyanide, protection of the resulting secondary alcohol and nitrile to carboxyl conversion afford, in good yields, protected β-hydroxy-γ-amino acid belonging to either the anti (erythro) or syn (threo) series. This methodology has been applied to the enantioselective preparation of cyclohexylstatine, a key component of several aspartyl protease inhibitors, in fully protected form.
A NOVEL SHORT AND EFFICIENT ASYMMETRIC SYNTHESIS OF STATINE ANALOGUES
Devant, Ralf M.,Radunz, Hans-E.
, p. 2307 - 2310 (2007/10/02)
The statine analogues 1a-c have been obtained in high optical purity via addition of chiral acetate enolate 4 to the α-aminoaldehydes 5a-c, followed by transesterification.