Stereoselective synthesis of 4,5-dihydroxy-D-erythro- and 4,5-dihydroxy-D-threo-L-norvaline from D-ribonolactone
Nitrogen functions have been introduced stereoselectively at the C-2 position in D-ribonolactone derivatives in order to prepared the title unnatural amino acids. The synthetic strategies lie in the inversion of configuration in S(N)2-type substitution re
Ariza,Diaz,Font,Ortuno
p. 1315 - 1326
(2007/10/02)
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