Addition of Nitrile Oxides to C60: Formation of Isoxazoline Derivatives of Fullerenes

Mark S. Meier; Magdalena Poplawska

doi:10.1021/jo00069a007

Addition of Nitrile Oxides to C₆₀: Formation of Isoxazoline Derivatives of Fullerenes

Mark S. Meier
, Magdalena Poplawska

Chemistry

Producción científica: Article › revisión exhaustiva

101 Citas (Scopus)

Resumen

Nitrile oxides add to C₆₀ in a 1,3-dipolar fashion. The nitrile oxides were generated in situ, and the products were isolated by gel permeation chromatography. Products with C₈ symmetry are indicated by the ¹³C NMR spectra, suggesting that the addition takes place across a 6,6 ring fusion.

Idioma original	English
Páginas (desde-hasta)	4524-4525
Número de páginas	2
Publicación	Journal of Organic Chemistry
Volumen	58
N.º	17
DOI	https://doi.org/10.1021/jo00069a007
Estado	Published - 1993

ASJC Scopus subject areas

Organic Chemistry

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10.1021/jo00069a007

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abstract = "Nitrile oxides add to C60 in a 1,3-dipolar fashion. The nitrile oxides were generated in situ, and the products were isolated by gel permeation chromatography. Products with C8 symmetry are indicated by the 13C NMR spectra, suggesting that the addition takes place across a 6,6 ring fusion.",

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Y1 - 1993

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AB - Nitrile oxides add to C60 in a 1,3-dipolar fashion. The nitrile oxides were generated in situ, and the products were isolated by gel permeation chromatography. Products with C8 symmetry are indicated by the 13C NMR spectra, suggesting that the addition takes place across a 6,6 ring fusion.

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JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

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