Thompson, David H. published the artcileSynthesis of Chiral Diether and Tetraether Phospholipids: Regiospecific Ring Opening of Epoxy Alcohol Intermediates Derived from Asymmetric Epoxidation, Formula: C9H9NO6S, the publication is Journal of Organic Chemistry (1994), 59(11), 2945-55, database is CAplus.
Diether and tetraether glycerophospholipids, e.g. I (R = CH2CH2N+Me2, R1 = C8H17, n = 16; R1 = C10H21, n = 20), have been synthesized using chiral epoxy alc. starting materials (e.g. glycidol 3-nitrobenzenesulfonate esters or tert-butyldiphenylsilyl ethers) via regioselective oxirane ring cleavage of epoxides, e.g. II.. These chiral precursors provide control over the stereochem., substitution patterns, and steric properties of the phosphoglycerol backbone. Bolaamphiphiles adopted a U-shaped conformation at the air-water interface.
Journal of Organic Chemistry published new progress about 115314-17-5. 115314-17-5 belongs to esters-buliding-blocks, auxiliary class Epoxides,Chiral,Nitro Compound,Sulfonate,Benzene, name is (R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate, and the molecular formula is C7H11N, Formula: C9H9NO6S.
Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics