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An approach to the Paal–Knorr pyrroles synthesis in the presence of β-cyclodextrin in aqueous media
引用本文:Fu-Jun Duan,Jin-Chang Ding,Hong-Juan Deng,Ding-Ben Chen,Jiu-Xi Chen,Miao-Chang Liu,Hua-Yue Wu. An approach to the Paal–Knorr pyrroles synthesis in the presence of β-cyclodextrin in aqueous media[J]. 中国化学快报, 2013, 24(9): 793-796. DOI: 10.1016/j.cclet.2013.05.012
作者姓名:Fu-Jun Duan  Jin-Chang Ding  Hong-Juan Deng  Ding-Ben Chen  Jiu-Xi Chen  Miao-Chang Liu  Hua-Yue Wu
作者单位:College of Chemistry and Materials Engineering, Wenzhou University;Wenzhou Vocational and Technical College;College of Pharmaceutical and Chemical Engineering, Taizhou University
基金项目:Wethank the National Natural Science Foundation of China(No. 21172175) and Natural Science Foundation of Zhejiang Province(Nos. LY12B02011 and Y4110491) for financial support.
摘    要:An efficient and facile method for the synthesis of N-substituted pyrroles in moderate to good yields by the Paal–Knorr reaction of γ-diketones with amines in the presence of β-cyclodextrin in aqueous media has been developed.Moreover,this process tolerated diamines(e.g.,para-,meta- or orthophenylenediamine)to construct bis-pyrrole or mono-pyrrole derivates.β-Cyclodextrin can be recovered easily after the reactions and reused without evident loss in activity.

关 键 词:Pyrrole  Paal–Knorr  β-Cyclodextrin  Water
收稿时间:2013-03-29
修稿时间:2013-05-07

An approach to the Paal-Knorr pyrroles synthesis in the presence of β-cyclodextrin in aqueous media
Fu-Jun Duan,Jin-Chang Ding,Hong-Juan Deng,Ding-Ben Chen,Jiu-Xi Chen,Miao-Chang Liu,Hua-Yue Wu. An approach to the Paal-Knorr pyrroles synthesis in the presence of β-cyclodextrin in aqueous media[J]. Chinese Chemical Letters, 2013, 24(9): 793-796. DOI: 10.1016/j.cclet.2013.05.012
Authors:Fu-Jun Duan  Jin-Chang Ding  Hong-Juan Deng  Ding-Ben Chen  Jiu-Xi Chen  Miao-Chang Liu  Hua-Yue Wu
Affiliation:a College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China;b Wenzhou Vocational and Technical College, Wenzhou 325035, China;c College of Pharmaceutical and Chemical Engineering, Taizhou University, Linhai 317000, China
Abstract:An efficient and facile method for the synthesis of N-substituted pyrroles in moderate to good yields by the Paal-Knorr reaction of γ-diketones with amines in the presence of β-cyclodextrin in aqueous media has been developed. Moreover, this process tolerated diamines(e.g., para-, meta-or ortho-phenylenediamine) to construct bis-pyrrole or mono-pyrrole derivates. β-Cyclodextrin can be recovered easily after the reactions and reused without evident loss in activity.
Keywords:Pyrrole  Paal-Knorr  &beta  -Cyclodextrin  Water
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