351340-32-4Relevant academic research and scientific papers
A strategy for the asymmetric aminohomologation of α,β-dihydroxy aldehydes: Application to the synthesis of the southwest tripeptide segment of echinocandin B
Palomo, Claudio,Oiarbide, Mikel,Landa, Aitor
, p. 41 - 46 (2007/10/03)
The synthesis of the (2S,3S,4S)-3,4-dihydroxyhomotyrosine amino acid segment, present in echinocandin B, in its activated form ready for peptide coupling is described. The key steps of the approach are the enantioselective AD reaction of 4-methoxycinnamic
