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

Hiroyuki Isobe; Masaya Sawamura; Eiichi Nakamura

doi:10.1080/10641229909351358

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

Hiroyuki Isobe, Masaya Sawamura, Eiichi Nakamura

Research output: Contribution to journal › Conference article › peer-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 language	English
Pages (from-to)	519-528
Number of pages	10
Journal	Fullerene Science and Technology
Volume	7
Issue number	4
DOIs	https://doi.org/10.1080/10641229909351358
Publication status	Published - 1999

ASJC Scopus subject areas

Chemical Engineering(all)

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10.1080/10641229909351358

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title = "Optical resolution of chirally functionalized [60]fullerene through formation of diastereomeric methoxyphenylacetic acid esters",

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.",

author = "Hiroyuki Isobe and Masaya Sawamura and Eiichi Nakamura",

year = "1999",

doi = "10.1080/10641229909351358",

language = "English",

volume = "7",

pages = "519--528",

journal = "Fullerenes Nanotubes and Carbon Nanostructures",

issn = "1536-383X",

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T1 - Optical resolution of chirally functionalized [60]fullerene through formation of diastereomeric methoxyphenylacetic acid esters

AU - Isobe, Hiroyuki

AU - Sawamura, Masaya

AU - Nakamura, Eiichi

PY - 1999

Y1 - 1999

N2 - 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.

AB - 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.

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U2 - 10.1080/10641229909351358

DO - 10.1080/10641229909351358

M3 - Conference article

AN - SCOPUS:0032599615

VL - 7

SP - 519

EP - 528

JO - Fullerenes Nanotubes and Carbon Nanostructures

JF - Fullerenes Nanotubes and Carbon Nanostructures

SN - 1536-383X

IS - 4

ER -

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

Abstract

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