Title of article
Easy access to N-alkylation of N-unsubstituted [60]fulleropyrrolidines: reductive amination using sodium triacetoxyborohydride
Author/Authors
Xiao، نويسنده , , Shengqiang and Li، نويسنده , , Yongjun and Li، نويسنده , , Yuliang and Liu، نويسنده , , Huibiao and Li، نويسنده , , Hongmei and Zhuang، نويسنده , , Junpeng and Liu، نويسنده , , Yang and Lu، نويسنده , , Fushen and Zhang، نويسنده , , Deqing and Zhu، نويسنده , , Daoben، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
4
From page
3975
To page
3978
Abstract
[60]Fulleropyrrolidines were used as secondary amines to react with aldehydes through reductive aminations 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.
Keywords
N-Alkylation , Sodium triacetoxyborohydride , reductive amination
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1841625
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