Selective synthesis of b-unsubstituted meso-aryl substituted tripyrranes in water
Joint Authors
Gu, Cheng Zhi
Feng, Ya Qing
Liu, Peng Peng
Meng, Shu Xian
Source
Journal of Saudi Chemical Society
Issue
Vol. 19, Issue 2 (31 Mar. 2015), pp.227-232, 6 p.
Publisher
Publication Date
2015-03-31
Country of Publication
Saudi Arabia
No. of Pages
6
Main Subjects
Topics
Abstract EN
A convenient method for the synthesis of b-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.
American Psychological Association (APA)
Gu, Cheng Zhi& Feng, Ya Qing& Liu, Peng Peng& Meng, Shu Xian. 2015. Selective synthesis of b-unsubstituted meso-aryl substituted tripyrranes in water. Journal of Saudi Chemical Society،Vol. 19, no. 2, pp.227-232.
https://search.emarefa.net/detail/BIM-546430
Modern Language Association (MLA)
Gu, Cheng Zhi…[et al.]. Selective synthesis of b-unsubstituted meso-aryl substituted tripyrranes in water. Journal of Saudi Chemical Society Vol. 19, no. 2 (Mar. 2015), pp.227-232.
https://search.emarefa.net/detail/BIM-546430
American Medical Association (AMA)
Gu, Cheng Zhi& Feng, Ya Qing& Liu, Peng Peng& Meng, Shu Xian. Selective synthesis of b-unsubstituted meso-aryl substituted tripyrranes in water. Journal of Saudi Chemical Society. 2015. Vol. 19, no. 2, pp.227-232.
https://search.emarefa.net/detail/BIM-546430
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 232
Record ID
BIM-546430
