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 |