Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride
文献类型:期刊论文
作者 | Xiao, SQ; Li, YJ; Li, YL; Liu, HB; Li, HM; Zhuang, JP; Liu, Y; Lu, FS; Zhang, DQ; Zhu, DB |
刊名 | TETRAHEDRON LETTERS
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出版日期 | 2004-05-10 |
卷号 | 45期号:20页码:3975-3978 |
关键词 | N-alkylation [60]Fulleropyrrolidines Reductive Amination Sodium Triacetoxyborohydride |
ISSN号 | 0040-4039 |
DOI | 10.1016/j.tetlet.2004.03.104 |
英文摘要 | [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. |
语种 | 英语 |
WOS记录号 | WOS:000221201900030 |
出版者 | PERGAMON-ELSEVIER SCIENCE LTD |
源URL | [http://ir.iccas.ac.cn/handle/121111/81557] ![]() |
专题 | 中国科学院化学研究所 |
通讯作者 | Zhu, DB |
作者单位 | 1.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 |
推荐引用方式 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. |
入库方式: OAI收割
来源:化学研究所
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