HFCAS OpenIR  > 中科院等离子体物理研究所
Cu(OAc)(2)-Mediated Reaction of [60]Fullerene with Aldehydes and Primary Amines for the Synthesis of Fulleropyrrolines
Wu, Jun1,2; Liu, Chun-Xiang1,2; Wang, Hui-Juan3; Li, Fa-Bao1,2; Shi, Ji-Long1,2; Liu, Li1,2; Li, Jia-Xing4; Liu, Chao-Yang3; Huang, Yong-Shun4
2016-10-07
发表期刊JOURNAL OF ORGANIC CHEMISTRY
摘要The facile one-step reaction of [60]fullerene with aldehydes and primary amines in the presence of cheap and easily available Cu(OAc)(2)center dot H2O afforded a series of new types of fulleropyrrolines with trisubstituted C=C bonds in good to excellent yields, which would be difficult to prepare by known methods. The formed fulleropyrroline under the assistance of Pd(OAc)(2) and CuCl2 center dot 2H(2)O could be further converted to 1-fulleropyrrolidine by the chlorohydroxylation reaction of C=C bond. Subsequent elimination reaction of 1-fulleropyrrolidine with the aid of TsOH center dot H2O generated the scarce 1-fulleropyrroline derivative.
文章类型Article
WOS标题词Science & Technology ; Physical Sciences
DOI10.1021/acs.joc.6b01875
关键词[WOS]ONE-STEP REACTION ; ASYMMETRIC CHLOROHYDRIN SYNTHESIS ; MANGANESE(III) ACETATE DIHYDRATE ; MEDIATED RADICAL REACTIONS ; FERRIC PERCHLORATE ; FACILE ACCESS ; 60 FULLERENE ; DERIVATIVES ; STEREOCHEMISTRY ; CHEMISTRY
收录类别SCI
语种英语
项目资助者National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; National Natural Science Foundation of China(21102041 ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Foundation of Hubei Province(2014CFB550) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Natural Science Fund for Creative Research Groups of Hubei Province of China(2014CFA015) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; Innovation and Entrepreneurship Training Program for Undergraduates of Hubei Province(201610512054) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236) ; 21272236)
WOS研究方向Chemistry
WOS类目Chemistry, Organic
WOS记录号WOS:000385054300059
引用统计
被引频次:27[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.hfcas.ac.cn:8080/handle/334002/21410
专题中科院等离子体物理研究所
作者单位1.Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ, Key Lab Synth & Applicat Organ Funct Mol, Wuhan 430062, Peoples R China
2.Hubei Univ, Sch Chem & Chem Engn, Wuhan 430062, Peoples R China
3.Chinese Acad Sci, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan Ctr Magnet Resonance, Wuhan Inst Phys & Math, Wuhan 430071, Peoples R China
4.Chinese Acad Sci, Inst Plasma Phys, Key Lab Novel Thin Film Solar Cells, POB 1126, Hefei 230031, Peoples R China
推荐引用方式
GB/T 7714
Wu, Jun,Liu, Chun-Xiang,Wang, Hui-Juan,et al. Cu(OAc)(2)-Mediated Reaction of [60]Fullerene with Aldehydes and Primary Amines for the Synthesis of Fulleropyrrolines[J]. JOURNAL OF ORGANIC CHEMISTRY,2016,81(19):9296-9307.
APA Wu, Jun.,Liu, Chun-Xiang.,Wang, Hui-Juan.,Li, Fa-Bao.,Shi, Ji-Long.,...&Huang, Yong-Shun.(2016).Cu(OAc)(2)-Mediated Reaction of [60]Fullerene with Aldehydes and Primary Amines for the Synthesis of Fulleropyrrolines.JOURNAL OF ORGANIC CHEMISTRY,81(19),9296-9307.
MLA Wu, Jun,et al."Cu(OAc)(2)-Mediated Reaction of [60]Fullerene with Aldehydes and Primary Amines for the Synthesis of Fulleropyrrolines".JOURNAL OF ORGANIC CHEMISTRY 81.19(2016):9296-9307.
条目包含的文件 下载所有文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可
Cu(OAc)(2)-Mediated (623KB)期刊论文作者接受稿开放获取CC BY-NC-SA浏览 下载
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Wu, Jun]的文章
[Liu, Chun-Xiang]的文章
[Wang, Hui-Juan]的文章
百度学术
百度学术中相似的文章
[Wu, Jun]的文章
[Liu, Chun-Xiang]的文章
[Wang, Hui-Juan]的文章
必应学术
必应学术中相似的文章
[Wu, Jun]的文章
[Liu, Chun-Xiang]的文章
[Wang, Hui-Juan]的文章
相关权益政策
暂无数据
收藏/分享
文件名: Cu(OAc)(2)-Mediated Reaction of [60]Fullerene with Aldehydes and Primary Amines for the Synthesis of Fulleropyrrolines.pdf
格式: Adobe PDF
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。