All articles of this category An acidic opening of the benzyl esters of D and L arabinal (1,5-anhydro-2-deoxy- erythro -pent-1-enitol) catalyzed by mercuric sulfate has been proposed as the key step in the preparation of chiral synthons with selectively substituted hydroxy groups.
No takes yet. Share an insight, caveat, or question.
Tolstikov et al. (1988) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: