Addition Reaction of Allylic Stannanes to the Triplet Excited State of C60 via Photoinduced Electron Transfer Process Leading to Asymmetric Hybridization Chemistry for Fullerene Terpenoid

Koichi Mikami; Shoji Matsumoto; Takayuki Tonoi; Tomoyoshi Suenobu; Akito Ishida; Shunichi Fukuzumi

doi:10.1055/s-1997-720

Addition Reaction of Allylic Stannanes to the Triplet Excited State of C₆₀ via Photoinduced Electron Transfer Process Leading to Asymmetric Hybridization Chemistry for Fullerene Terpenoid

Koichi Mikami, Shoji Matsumoto, Takayuki Tonoi, Tomoyoshi Suenobu, Akito Ishida, Shunichi Fukuzumi

応用化学科

研究成果: Article › 査読

25 被引用数 (Scopus)

抄録

Addition of allylic stannanes to C₆₀ takes place under UV-irradiation in benzene as well as benzonitrile to yield the allylic fullerenes, of which the asymmetric version with pinene-derived chiral allylic stannane leads to an enantio-pure fullerene terpenoid.

本文言語	English
ページ（範囲）	85-87
ページ数	3
ジャーナル	Synlett
巻	1997
号	1
DOI	https://doi.org/10.1055/s-1997-720
出版ステータス	Published - 1997

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10.1055/s-1997-720

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引用スタイル

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abstract = "Addition of allylic stannanes to C60 takes place under UV-irradiation in benzene as well as benzonitrile to yield the allylic fullerenes, of which the asymmetric version with pinene-derived chiral allylic stannane leads to an enantio-pure fullerene terpenoid.",

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AU - Tonoi, Takayuki

AU - Suenobu, Tomoyoshi

AU - Ishida, Akito

AU - Fukuzumi, Shunichi

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AB - Addition of allylic stannanes to C60 takes place under UV-irradiation in benzene as well as benzonitrile to yield the allylic fullerenes, of which the asymmetric version with pinene-derived chiral allylic stannane leads to an enantio-pure fullerene terpenoid.

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