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...
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 |
Similar Items
-
The first direct synthesis of β-unsubstituted meso-decamethylcalix[5]pyrrole
by: Luis Chacón-García, et al.
Published: (2009-01-01) -
An Efficient Synthesis of Aryl-Substituted Pyrroles by the Suzuki–Miyaura Coupling Reaction of SEM-Protected Pyrroles
by: Keli Cui, et al.
Published: (2019-04-01) -
Three-component reactions of aromatic amines, 1,3-dicarbonyl compounds, and α-bromoacetaldehyde acetal to access N-(hetero)aryl-4,5-unsubstituted pyrroles
by: Wenbo Huang, et al.
Published: (2020-11-01) -
Unexpected Synthesis of a Bulky Bis-Pocket A3B-Type Meso-Cyano Porphyrin
by: Ze-Yu Liu, et al.
Published: (2017-11-01) -
The reductive condensation of 2,5-disubstituted pyrroles
by: White, James David
Published: (2012)