@article {3912,
	title = {5,10-Diphenyltripyrrane, a useful building block for the synthesis of meso-phenyl substituted expanded macrocycles},
	journal = {Chemical Communications},
	number = {17},
	year = {1997},
	note = {ISI Document Delivery No.: XW022Times Cited: 62Cited Reference Count: 22},
	month = {Sep},
	pages = {1689-1690},
	type = {Article},
	abstract = {Pyrrole and benzaldehyde were condensed under acidic conditions to produce a mixture of 5-phenyldipyrromethane and 5,10-diphenyltripyrrane; the tripyrrane was utilized in syntheses of meso-phenylsapphyrins, meso-diphenylpentaphyrin and meso-hexaphenylhexaphyrin.},
	keywords = {PORPHOCYANINES, PORPHYRIN},
	isbn = {1359-7345},
	url = {<Go to ISI>://A1997XW02200050},
	author = {Bruckner, C. and Sternberg, E. D. and Boyle, R. W. and Dolphin, D.}
}
@article {2971,
	title = {MESO-PHENYL SUBSTITUTED PORPHOCYANINES - A NEW CLASS OF FUNCTIONALIZED EXPANDED PORPHYRINS},
	journal = {Tetrahedron Letters},
	volume = {35},
	number = {30},
	year = {1994},
	note = {ISI Document Delivery No.: NY923Times Cited: 18Cited Reference Count: 11},
	month = {Jul},
	pages = {5377-5380},
	type = {Article},
	abstract = {Porphocyanines bearing phenyl substituents at both or one of the two available mesopositions have been synthesised. Derivatives have also been synthesised with substituents on the phenyl rings and both alkyl and unsubstituted pyrrolic beta-positions.},
	keywords = {BIOLOGICAL-ACTIVITIES, EXPANDED PORPHYRINS, INVITRO, PHOTODYNAMIC THERAPY, PHOTOTOXICITY, PORPHOCYANINES, TUMOR, ZINC PHTHALOCYANINES},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1994NY92300015},
	author = {Boyle, R. W. and Xie, L. Y. and Dolphin, D.}
}
