TY - JOUR
T1 - Unusual peptides containing the 2,6-diaminopimelic acid framework
T2 - Stereocontrolled synthesis, X-ray analysis, and computational modelling. Part 2
AU - Galeazzi, R.
AU - Garavelli, M.
AU - Grandi, A.
AU - Monari, M.
AU - Porzi, G.
AU - Sandri, S.
PY - 2003/9/5
Y1 - 2003/9/5
N2 - The stereocontrolled synthesis of peptides 6, 9 and 14, structural variants of 2,6-diaminopimelic acid, was carried out starting from the chiral synthon 1, easily obtained from L-valine. The configuration of the introduced stereogenic centres has been assigned on the basis of 1H NMR spectroscopic data. X-Ray crystal structure and conformation analysis of 5 are also reported.
AB - The stereocontrolled synthesis of peptides 6, 9 and 14, structural variants of 2,6-diaminopimelic acid, was carried out starting from the chiral synthon 1, easily obtained from L-valine. The configuration of the introduced stereogenic centres has been assigned on the basis of 1H NMR spectroscopic data. X-Ray crystal structure and conformation analysis of 5 are also reported.
UR - http://www.scopus.com/inward/record.url?scp=0041829504&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0041829504&partnerID=8YFLogxK
U2 - 10.1016/S0957-4166(03)00541-X
DO - 10.1016/S0957-4166(03)00541-X
M3 - Article
AN - SCOPUS:0041829504
VL - 14
SP - 2639
EP - 2649
JO - Tetrahedron Asymmetry
JF - Tetrahedron Asymmetry
SN - 0957-4166
IS - 17
ER -