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...
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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 |