Answers are grounded in this paper and cite their sources.
The direct resolution of (3aRS, 6SR, 6aSR)-1, 3-dibenzyl-6-hydroxy-3, 3a, 6, 6a-tetrahydro-1H-furo[3, 4-d]imidazole-2, 4-dione [(±)-9], a key intermediate for biotin, with optically active amines was examined. Reaction of (±)-9 with cinchonidine readili gave the cinchonidine salt of the (4S, 5R)-aldehyde-carboxylic acid (12), acidification of which gave (3aS.6R, 6aR)-9, convertible to biothin. N-alkyl-D-glucamines (14) were also found to be effective resolving agents for (±)-9 applicable for industrial use. Reutilizatin of the unwanted epimer [(3aR, 6S, 6aS)-9] was effected by facile oxidation to the meso-diacid (3) with sodium chlorite.
No takes yet. Share an insight, caveat, or question.
Senuma et al. (1990) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: