Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4012
Title: Cyclic Dipeptides - A Stereocontrolled Synthesis of (2s,3r,6r) and (2r,3r,6r)-6-tert-butoxycarbonylamino-3-methoxycarbonyl-2-methyl-5-oxope Rhydro-1,4-thiazepine
Authors: Corelli, Federico 
A., Crescenza
D., Dei
Taddei, Maurizio 
Botta, Maurizio 
Issue Date: 1994
Project: None 
Journal: TETRAHEDRON-ASYMMETRY
Abstract: 
A stereselective synthesis of the title compounds, starting from commercially available amino acids, is described. The absolute stereochemistry of 3a and 3b has been deduced on the basis of H-1 NMR and chemical degradation studies. The formation of only these two isomers has been rationalized in terms of molecular mechanics calculations.
Description: 
45953
URI: http://hdl.handle.net/20.500.12779/4012
ISSN: 0957-4166
DOI: 10.1016/0957-4166(94)80115-0
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