Extremely stereoselective and stereospecific reductive cleavage of .beta.-lactams. A highly efficient route to labeled homochiral peptides
- 1 May 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 108 (11) , 3100-3102
- https://doi.org/10.1021/ja00271a048
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Synthesis of chiral oligopeptides by means of catalytic asymmetric hydrogenation of dehydropeptidesTetrahedron, 1984
- Tritiated peptides. Part 141. Catalytic exchange labelling of various synthetic peptidesJournal of Labelled Compounds and Radiopharmaceuticals, 1983
- Synthesis of chiral dipeptides by means of asymmetric hydrogenation of dehydro dipeptidesThe Journal of Organic Chemistry, 1982
- Asymmetric tritiation of N-acetyl dehydrophenylalanyl-(S) phenylalanine (methylester) catalyzed with a rhodium (+) diop complexTetrahedron, 1982