675608-60-3Relevant academic research and scientific papers
Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems
Miyake, Kae,Lash, Timothy D.
, p. 178 - 179 (2004)
Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmethyl)benzene derivatives in moderate yields; these afforded a series of novel aromatic benziporphyrins using the MacDonald "3 + 1"
Synthesis of a series of aromatic benziporphyrins and heteroanalogues via tripyrrane-like intermediates derived from resorcinol and 2-methylresorcinol
Lash, Timothy D.,Miyake, Kae,Xu, Linlin,Ferrence, Gregory M.
, p. 6295 - 6308 (2011)
Tripyrrane analogues were prepared by reacting resorcinol or 2-methylresorcinol with 2 equiv of an acetoxymethylpyrrole in the presence of p-toluenesulfonic acid and calcium chloride. Following removal of the benzyl ester protective groups, the resorcinol
Synthesis of aromatic dicarbaporphyrinoids from resorcinol and 2-methylresorcinol
Xu, Linlin,Lash, Timothy D.
, p. 8863 - 8866 (2007/10/03)
23-Carba-oxybenziporphyrins, a new group of dicarbaporphyrinoids, are easily prepared by reacting tripyrrane analogues derived from resorcinol or 2-methylresorcinol with an indene dialdehyde under MacDonald '3+1' conditions.
