1382153-84-5Relevant articles and documents
A stereoselective synthesis of an α-substituted α-amino acid as a substructure for the construction of myriocin
Martinkova, Miroslava,Gonda, Jozef,Raschmanova, Jana Spakova,Kuchar, Juraj,Kozisek, Jozef
, p. 536 - 546 (2012)
A synthetic route to the protected quaternary α-amino acid 2 with a hydroxylated side chain has been achieved. The key transformations are the diastereoselective substrate-controlled epoxidation of allylic alcohol 4; a highly stereoselective oxidation-reduction protocol, and the excellent regioselective isomerization of the oxazolidinone ring to give an oxazinanone skeleton in derivative 3. The carboxylic acid 2 obtained represents the polar substructure, which is present in myriocin 1.