Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water

A convenient method for the synthesis of β-unsubstituted meso-aryl substituted tripyrranes was developed. Pyrrole condensed with aldehyde in acidic aqueous to produce tripyrranes selectively in moderate yield. The selectivity for tripyrranes depended on the electronic and steric properties of aldehy...

Full description

Bibliographic Details
Main Authors: Cheng-Zhi Gu, Ya-Qing Feng, Peng-Peng Liu, Shu-Xian Meng
Format: Article
Language:English
Published: Elsevier 2015-03-01
Series:Journal of Saudi Chemical Society
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319610314000696
id doaj-e491b54431194b0080f409d806184484
record_format Article
spelling doaj-e491b54431194b0080f409d8061844842020-11-24T23:07:08ZengElsevierJournal of Saudi Chemical Society1319-61032015-03-0119222723210.1016/j.jscs.2014.05.004Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in waterCheng-Zhi Gu0Ya-Qing Feng1Peng-Peng Liu2Shu-Xian Meng3School of Chemical Engineering, TianJin University, Tianjin 300072, PR ChinaSchool of Chemical Engineering, TianJin University, Tianjin 300072, PR ChinaSchool of Chemical Engineering, TianJin University, Tianjin 300072, PR ChinaSchool of Chemical Engineering, TianJin University, Tianjin 300072, PR ChinaA convenient method for the synthesis of β-unsubstituted meso-aryl substituted tripyrranes was developed. Pyrrole condensed with aldehyde in acidic aqueous to produce tripyrranes selectively in moderate yield. The selectivity for tripyrranes depended on the electronic and steric properties of aldehyde, the stoichiometric molar ratio and concentrations of the starting materials. The title compounds were isolated and characterized by 1H NMR, 13C NMR and HR-MS analysis.http://www.sciencedirect.com/science/article/pii/S1319610314000696TripyrranePyrroleCondensationWaterSelectivity
collection DOAJ
language English
format Article
sources DOAJ
author Cheng-Zhi Gu
Ya-Qing Feng
Peng-Peng Liu
Shu-Xian Meng
spellingShingle Cheng-Zhi Gu
Ya-Qing Feng
Peng-Peng Liu
Shu-Xian Meng
Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
Journal of Saudi Chemical Society
Tripyrrane
Pyrrole
Condensation
Water
Selectivity
author_facet Cheng-Zhi Gu
Ya-Qing Feng
Peng-Peng Liu
Shu-Xian Meng
author_sort Cheng-Zhi Gu
title Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
title_short Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
title_full Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
title_fullStr Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
title_full_unstemmed Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
title_sort selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
publisher Elsevier
series Journal of Saudi Chemical Society
issn 1319-6103
publishDate 2015-03-01
description A convenient method for the synthesis of β-unsubstituted meso-aryl substituted tripyrranes was developed. Pyrrole condensed with aldehyde in acidic aqueous to produce tripyrranes selectively in moderate yield. The selectivity for tripyrranes depended on the electronic and steric properties of aldehyde, the stoichiometric molar ratio and concentrations of the starting materials. The title compounds were isolated and characterized by 1H NMR, 13C NMR and HR-MS analysis.
topic Tripyrrane
Pyrrole
Condensation
Water
Selectivity
url http://www.sciencedirect.com/science/article/pii/S1319610314000696
work_keys_str_mv AT chengzhigu selectivesynthesisofbunsubstitutedmesoarylsubstitutedtripyrranesinwater
AT yaqingfeng selectivesynthesisofbunsubstitutedmesoarylsubstitutedtripyrranesinwater
AT pengpengliu selectivesynthesisofbunsubstitutedmesoarylsubstitutedtripyrranesinwater
AT shuxianmeng selectivesynthesisofbunsubstitutedmesoarylsubstitutedtripyrranesinwater
_version_ 1725619841097793536