Cyclic Oligofurans: One-Pot Synthesis of 30π and 40π Expanded Porphyrinoids

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DC Field	Value	Language
dc.contributor.author	Reddy, J S	-
dc.contributor.author	Mandal, S	-
dc.contributor.author	Anand, V G	-
dc.date.accessioned	2017-02-16T08:50:04Z	-
dc.date.available	2017-02-16T08:50:04Z	-
dc.date.issued	2006-11-23	-
dc.identifier.citation	Organic Letters, 8(24):5541-5543	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2677	-
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 30π and 40π 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.title	Cyclic Oligofurans: One-Pot Synthesis of 30π and 40π Expanded Porphyrinoids	en_US
dc.type	Article	en_US
Appears in Collections:	2006

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