38146-56-4Relevant academic research and scientific papers
SYNTHESIS OF 2S,4S,5S-DIHYDROXYPIPECOLIC ACID AND BULGECININE FROM D-GLUCURONOLACTONE; A STRATEGY FOR THE SYNTHESIS OF 2S,4S-4-HYDROXY-α-AMINO ACIDS
Bashyal, Bharat P.,Chow, Hak-Fun,Fleet, George W. J.
, p. 423 - 430 (2007/10/02)
The efficient synthesis of 4S,5S-2-(N-benzyloxycarbonyl)amino-5,6-dihydrohex-2-en-4-olide (4) from D-glucuronolactone is described; the potential of (4) as a divergent intermediate for the synthesis of 2S,4S-4-hydroxy-α-amino acids is illustrated by the c
ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM D-GLUCURONOLACTONE
Bashyal, B. P.,Chow, H.-F.,Fleet, G. W. J.
, p. 3205 - 3208 (2007/10/02)
The potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine.
