N-tert-butoxycarbonyl-2-(tert-butyldimethylsiloxy)pyrrole as a glycine anion equivalent: A flexible enantioselective access to polyhydroxy-α-amino acids

Add time:09/08/2019    Source:sciencedirect.com

An efficient stereoselective route to polyhydroxy-α-amino acids 7a-f was developed by exploiting N-tert-butoxycarbonyl-2-(tert-butyldimethylsiloxy)pyrrole as a glycine anion equivalent.

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