@article {581, title = {3,3 {\textquoteright}-Dipyrrolyl sulfides, useful building blocks for the syntheses of macrocycles containing dipyrromethene units}, journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie}, volume = {81}, number = {9}, year = {2003}, note = {ISI Document Delivery No.: 721MBTimes Cited: 1Cited Reference Count: 18}, month = {Sep}, pages = {988-991}, type = {Article}, abstract = {5,5{\textquoteright}-Dicarboxy-3,3{\textquoteright}-dipyrrolyl sulfide was condensed with 5,5{\textquoteright}-diformyl-3,3{\textquoteright}-dipyrrolyl sulfide or 5,5{\textquoteright}-diformyldipyrromethane under acidic conditions to produce, in high yields, macrocycles containing four dipyrromethene units.}, keywords = {3, 3-dipyrrolyl sulfide, cyclopolypyrrole, dipyrromethene, EXPANDED PORPHYRINS, EXTRUSION, macrocycle}, isbn = {0008-4042}, url = {://000185319200004}, author = {Chen, Q. Q. and Dolphin, D.} } @article {5034, title = {A highly efficient preparation of N-confused cyclodecapyrroles}, journal = {Tetrahedron Letters}, volume = {42}, number = {19}, year = {2001}, note = {ISI Document Delivery No.: 427KUTimes Cited: 4Cited Reference Count: 33}, month = {May}, pages = {3263-3265}, type = {Article}, abstract = {Cyclodecapyrroles, potential novel host systems, were synthesized in 78-88\% yields by condensation of tripyrrane dialdehyde with bis(5-carboxyl-2,4-dimethyl-pyrrole-3-yl)-methane, ethane, and -propane in the presence of HBr and TFA. (C) 2001 Elsevier Science Ltd. All rights reserved.}, keywords = {3, 3 {\textquoteright}-dipyrromethane, ANION SENSORS, CALIXPYRROLES, CYCLOOCTAPYRROLES, cyclopolypyrrole, EXPANDED PORPHYRINS, HOST, macrocycle, macrocycles, METAL-COMPLEXES, TRIPYRRANE}, isbn = {0040-4039}, url = {://000168404000006}, author = {Chen, Q. Q. and Dolphin, D.} }