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Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride
Xiao, SQ; Li, YJ; Li, YL; Liu, HB; Li, HM; Zhuang, JP; Liu, Y; Lu, FS; Zhang, DQ; Zhu, DB
2004-05-10
Source PublicationTETRAHEDRON LETTERS
ISSN0040-4039
Volume45Issue:20Pages:3975-3978
Abstract[60]Fulleropyrrolidines were used as secondary amines to react with aldehydes through reductive animations to afford N-alkylated derivatives. In spite of the very weak base activity of the nitrogen atom of N-unsubstituted [60]fulleropyrrolidines, this method was found to be efficient at the aid of sodium triacetoxyborohydride. Several N-alkylated derivatives were synthesized and fully characterized. (C) 2004 Elsevier Ltd. All rights reserved.
KeywordN-alkylation [60]Fulleropyrrolidines Reductive Amination Sodium Triacetoxyborohydride
DOI10.1016/j.tetlet.2004.03.104
Indexed BySCI ; IC
Language英语
WOS IDWOS:000221201900030
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Cited Times:28[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/81558
Collection中国科学院化学研究所
Corresponding AuthorZhu, DB
Affiliation1.Chinese Acad Sci, Inst Chem, CAS, Key Lab Organ Solids, Beijing 100080, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Xiao, SQ,Li, YJ,Li, YL,et al. Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride[J]. TETRAHEDRON LETTERS,2004,45(20):3975-3978.
APA Xiao, SQ.,Li, YJ.,Li, YL.,Liu, HB.,Li, HM.,...&Zhu, DB.(2004).Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride.TETRAHEDRON LETTERS,45(20),3975-3978.
MLA Xiao, SQ,et al."Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride".TETRAHEDRON LETTERS 45.20(2004):3975-3978.
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