Cyclic oligofurans: one-pot synthesis of 30 pi and 40 pi expanded porphyrinoids

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Title:	Cyclic oligofurans: one-pot synthesis of 30 pi and 40 pi expanded porphyrinoids
Authors:	Reddy, J S Mandal, S Anand, V G
Keywords:	Structural characterization Dication Cyclopolypyrroles Macrocycles Octaphyrin Planar
Issue Date:	2006
Publisher:	American Chemical Society
Citation:	Organic Letters 8(24):5541-5543;23 Nov 2006
Abstract:	Acid-catalyzed condensation of furan and pentafluorobenzaldehyde yielded conjugated macrocycles with six and eight furan rings. They represent systems similar to annulenes with 30 d and 40 d electrons. From their structural analyses, it was found that furan rings in both the molecules were inverted in an alternative fashion and displayed nontwisted conformations.
URI:	http://10.10.100.66:8080/xmlui/handle/123456789/3525
ISSN:	1523-7060
Appears in Collections:	2006

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