Murthy, Satya S. published the artcileA facile stereospecific synthesis of the [2H6]-isopropyl-labeled metoprolol enantiomers from (2R)- and (2S)-glycidyl 3-nitrobenzenesulfonate, SDS of cas: 115314-17-5, the publication is Journal of Labelled Compounds and Radiopharmaceuticals (1990), 28(12), 1410-16, database is CAplus.
Enantiomers of metoprolol, e.g. I, containing six deuterium atoms in the iso-Pr Me groups were prepared in two steps from the sodium salt of 4-(2-methoxyethyl)phenol and the com. available (2R)- and (2S)-glycidyl 3-nitrobenzenesulfonate. The resulting (2R)- and (2S)-epoxides were opened using [2H6]-isopropylamine. The enantiomeric excesses were 93 and 95% for the deuterated (2R)- and (2S)-enantiomers of metoprolol as determined by chiral column HPLC.
Journal of Labelled Compounds and Radiopharmaceuticals 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 C9H9NO6S, SDS of cas: 115314-17-5.
Referemce:
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