# name
Stereoselective synthesis of protected peptides containing an anti β‐Hydroxy tyrosine

# metadata.dc.description.abstract[].value
Protected peptides containing an anti b-hydroxy tyrosine are synthesized in a straightforward and highly efficient manner through the direct and stereoselective addition of N-azidoacetyl-4-isopropyl-1,3-thiazolidine-2-thione to dialkyl acetals catalyzed by a nickel(II) complex, the forging of an amide bond by removal of the chiral auxiliary with an amino ester, and final coupling with a third amino acid.

# metadata.dc.relation.ispartof[].value
European Journal of Organic Chemistry, 2019, vol. 2019, num. 16, p. 2745-2752

# metadata.dc.source[].value
Articles publicats en revistes (Química Inorgànica i Orgànica)

# metadata.dc.title[].value
Stereoselective synthesis of protected peptides containing an anti β‐Hydroxy tyrosine