An efficient stereoselective route to polyhydroxy-alfa-amino acids 7a-f was developed by exploiting N-tert-butoxycarbonyl-2-(tert-butyldimetylsiloxy)pyrrole as a glycine anion equivalent
N-tert-BUTOXYCARBONYL-2-(tert-BUTYLDIMETHYLSILOXY)PYRROLE AS A GLYCINE ANION EQUIVALENT: A FLEXIBLE ENANTIOSELECTIVE ACCESS TO POLYHYDROXY-alfa-AMINO ACIDS
Pietro Spanu;
1994
Abstract
An efficient stereoselective route to polyhydroxy-alfa-amino acids 7a-f was developed by exploiting N-tert-butoxycarbonyl-2-(tert-butyldimetylsiloxy)pyrrole as a glycine anion equivalentFile in questo prodotto:
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