TY - JOUR
T1 - Syntheses of optically pure, conformationally constrained, and highly hydrophobic unusual amino acids
T2 - 2-Amino-3, 3-diarylpropionic acids
AU - Lin, J.
AU - Liao, S.
AU - Hruby, V. J.
PY - 2005/1
Y1 - 2005/1
N2 - A series of optically pure, conformationally constrained, and highly hydrophobic unusual aromatic amino acids, 2-amino-3,3-diarylpropionic acids, were synthesized via asymmetric 1,4-Michael addition reaction/azidation reactions in seven steps with overall yields of 20-30%.
AB - A series of optically pure, conformationally constrained, and highly hydrophobic unusual aromatic amino acids, 2-amino-3,3-diarylpropionic acids, were synthesized via asymmetric 1,4-Michael addition reaction/azidation reactions in seven steps with overall yields of 20-30%.
KW - Aromatic amino acids
KW - Asymmetric synthesis
KW - Conformationally constrained amino acids
UR - http://www.scopus.com/inward/record.url?scp=14044259963&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=14044259963&partnerID=8YFLogxK
U2 - 10.1111/j.1399-3011.2004.00194.x
DO - 10.1111/j.1399-3011.2004.00194.x
M3 - Article
C2 - 15686541
AN - SCOPUS:14044259963
SN - 1397-002X
VL - 65
SP - 105
EP - 112
JO - Journal of Peptide Research
JF - Journal of Peptide Research
IS - 1
ER -