Easy Access to [60]Fulleroalkaloids <i>via</i> Photoinduced Reactions of Tertiary Amines with [60]Fullerene
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- Li-Wei Guo
- Department of Chemistry, Fudan UniversityShanghai 200433, P.R . China
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- Xiang Gao
- Department of Chemistry, Fudan UniversityShanghai 200433, P.R . China
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- Dan-Wei Zhang
- Department of Chemistry, Fudan UniversityShanghai 200433, P.R . China
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- Shi-Hui Wu
- Department of Chemistry, Fudan UniversityShanghai 200433, P.R . China
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- Hou-Ming Wu
- State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic ChemistryShanghai 200032, P.R . China
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- Yong-Jiang Li
- State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic ChemistryShanghai 200032, P.R . China
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Abstract
<jats:title>Abstract</jats:title> <jats:p>Photoinduced reactions of tertiary amines with [60]fullerene (C60) were successfully applied to the synthesis of [60]fulleroalkaloids. This method is easy and effective for constructing C60 derivatives containing natural alkaloids for the purpose of checking the influence of the carbon cage on the biological activities of the alkaloids. In this letter, the preparation and characterization of [60]fulleroscandine is reported.</jats:p>
Journal
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- Chemistry Letters
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Chemistry Letters 28 (5), 411-412, 1999-05-01
Oxford University Press (OUP)
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Keywords
Details 詳細情報について
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- CRID
- 1360846644039797504
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- NII Article ID
- 10004341521
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- NII Book ID
- AA00603318
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- ISSN
- 13480715
- 03667022
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- Data Source
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- Crossref
- CiNii Articles