Simple methodology for the synthesis of meso-unsubstituted β-substituted alkyl porphyrins
S Juillard, G Simonneaux
Index: Juillard, Sandrine; Simonneaux, Gerard Synlett, 2006 , # 17 p. 2818 - 2820
Full Text: HTML
Citation Number: 2
Abstract
In our strategy, 1,9-diformyldipyrromethanes 6c and 7c [7] were the key intermediates (Figure [2] ). We first turned to the new dipyrromethane diester 6a, which was prepared from condensation of ethyl 5-acetoxymethyl-4-ethyl-3-methylpyrrole-2-carboxylate with ethyl pyrrole-2-carboxylate in the presence of p-toluenesulfonic acid in dichloromethane solution. The mixture was heated under nitrogen at 40 °C for 48 hours giving 6a in 53% yield. The prerequisite ...
Related Articles:
[Lash, Timothy D.; Chen, Shaohua Tetrahedron, 2005 , vol. 61, # 49 p. 11577 - 11600]
[Lash, Timothy D.; Chen, Shaohua Tetrahedron, 2005 , vol. 61, # 49 p. 11577 - 11600]
[Lash, Timothy D.; Chen, Shaohua Tetrahedron, 2005 , vol. 61, # 49 p. 11577 - 11600]
[Lash, Timothy D.; Chen, Shaohua Tetrahedron, 2005 , vol. 61, # 49 p. 11577 - 11600]
[Hombrecher, Hermann K.; Horter, Gaby Liebigs Annalen der Chemie, 1991 , # 3 p. 219 - 227]