Stereoselective synthesis of sterically constrained dipeptides. Part 2
摘要:
The alkylation of the diastereomeric mixture of lactims 2 and 3 occurs in total regioselectivity and good to high facial stereoselectivity (d.s. ranging from 82 to 97%). Cleavage of the lactim 4e gives enantiomerically pure dipeptide 12, sterically constrained at the alpha-carbon. The absolute configuration of the new stereocentres has been assigned on the basis of H-1-NMR data and NOE measurements. (C) 1998 Elsevier Science Ltd. All rights reserved.
Stereoselective synthesis of sterically constrained dipeptides. Part 2
摘要:
The alkylation of the diastereomeric mixture of lactims 2 and 3 occurs in total regioselectivity and good to high facial stereoselectivity (d.s. ranging from 82 to 97%). Cleavage of the lactim 4e gives enantiomerically pure dipeptide 12, sterically constrained at the alpha-carbon. The absolute configuration of the new stereocentres has been assigned on the basis of H-1-NMR data and NOE measurements. (C) 1998 Elsevier Science Ltd. All rights reserved.