Optical resolution of chirally functionalized [60]fullerene through formation of diastereomeric methoxyphenylacetic acid esters

Hiroyuki Isobe, Masaya Sawamura, Eiichi Nakamura

    Research output: Contribution to journalConference articlepeer-review

    7 Citations (Scopus)

    Abstract

    Optical resolution of chirally functionalized [60]fullerene has been achieved through formation of diastereomeric α-methoxyphenylacetic acid (MPA) esters. The diastereomeric ester products were easily separated either by open column silica gel chromatography or by high pressure liquid chromatography (HPLC) with BuckyPrep column.

    Original languageEnglish
    Pages (from-to)519-528
    Number of pages10
    JournalFullerene Science and Technology
    Volume7
    Issue number4
    DOIs
    Publication statusPublished - 1999

    ASJC Scopus subject areas

    • Chemical Engineering(all)

    Fingerprint

    Dive into the research topics of 'Optical resolution of chirally functionalized [60]fullerene through formation of diastereomeric methoxyphenylacetic acid esters'. Together they form a unique fingerprint.

    Cite this