I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
They are found as constituents of an increasing group of biologically active peptides. Stereocontrolled syntheses of chiral and racemic key intermediates to thienamycin from d-allo-threonine and trans-crotonic acid.
Peter Wipf,; Chris P. Miller. Stereospecific synthesis of peptide analogs with allo-threonine and D-allo-threonine residues . J. Org. Chem.. 1993, 58 (6),1575-1578.
Masao Shiozaki,; Noboru Ishida,; Hiroshi Maruyama,; Tetsuo Hiraoka. Stereocontrolled syntheses of chiral and racemic key intermediates to thienamycin from d-allo-threonine and trans-crotonic acid. Tetrahedron. 1983, 39(14),2399-2407.