The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 2,6-Dimethyl-3,5-heptanedione( cas:18362-64-6 ) is researched.Application of 18362-64-6.Jacoby, C.; Braekman, J. C.; Daloze, D. published the article 《Asymmetric synthesis of (3R,5R)- and (3S,5S)-2,6-dimethylheptane-3,5-diol, useful C2 chiral auxiliaries》 about this compound( cas:18362-64-6 ) in Tetrahedron: Asymmetry. Keywords: asym preparation dimethylheptanediol chiral auxiliary. Let’s learn more about this compound (cas:18362-64-6).
(R,R)- and (S,S)-2,6-dimethylheptane-3,5-diol, which are useful C2 chiral auxiliaries, have been both synthesized in high optical purity from 2,6-dimethylheptane-3,5-dione, by using as key step a Sharpless kinetic resolution
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Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica