104945-87-1Relevant articles and documents
SYNTHESIS OF 2R,3S,4R-DIHYDROXYPROLINE FROM D-RIBONOLACTONE
Dho, J. C.,Fleet, G. W. J.,Peach, J. M.,Prout, K.,Smith, P. W.
, p. 3203 - 3204 (1986)
A synthesis of 2R,3S,4R-dihydroxyproline is described in which an azide is introduced into C-2 position of D-ribonolactone with retention of configuration.
An efficient and concise entry to (-)-4,5-dihydroxy-d-threo-l norvaline. Formal synthesis of clavalanine
Ariza, Jesus,Font, Josep,Ortuno, Rosa M.
, p. 1979 - 1982 (2007/10/02)
The title amino acid (2) has been synthesized for the first time in a seven-step sequence from D-ribonolactone, in 20% overall yield. Since the N-carbamoyl derivative of (2) in its y-lactone form has been used to prepare clavalanine, a formal total synthe