@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 = {<Go to ISI>://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 = {<Go to ISI>://000168404000006},
	author = {Chen, Q. Q. and Dolphin, D.}
}
