Lok, C. M.; Ward, J. P.; Van Dorp, D. A. published the article 《The synthesis of chiral glycerides starting from D- and L-serine》. Keywords: glyceride chiral synthesis serine.They researched the compound: (2S)-(+)-3-Chloropropane-1,2-diol( cas:60827-45-4 ).HPLC of Formula: 60827-45-4. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:60827-45-4) here.
Chiral glycerides were prepared starting from D- and L-serine by a multistep stereospecific sequence. E.g., L-serine was converted by diazotization and esterification into Me L-glycerate, this by acetalization and reduction to 2,3-O-isopropylidene-sn-glycerol, which was converted by sequential chlorination, hydrolysis, and cyclocondensation to D-glycidol (I). I could be acylated, then esterified with a fatty acid to give a diglyceride mixture, which could be isomerized by heating to 100% 1,3-diglycerides, or its hydroxyl group could be protected by a trityl group and it could be converted into a 1,2-diglyceride. Both types of diglycerides could be converted conventionally into sn-triglycerides.
After consulting a lot of data, we found that this compound(60827-45-4)HPLC of Formula: 60827-45-4 can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com