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

dc.contributor.author	Reddy, J S
dc.contributor.author	Mandal, S
dc.contributor.author	Anand, V G
dc.date.accessioned	2020-02-25T12:36:02Z
dc.date.available	2020-02-25T12:36:02Z
dc.date.issued	2006
dc.identifier.citation	Organic Letters 8(24):5541-5543;23 Nov 2006	en_US
dc.identifier.issn	1523-7060
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3525
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Structural characterization	en_US
dc.subject	Dication	en_US
dc.subject	Cyclopolypyrroles	en_US
dc.subject	Macrocycles	en_US
dc.subject	Octaphyrin	en_US
dc.subject	Planar	en_US
dc.title	Cyclic oligofurans: one-pot synthesis of 30 pi and 40 pi expanded porphyrinoids	en_US
dc.type	Article	en_US