Cyclic oxyphosphoranes with six-and seven-membered rings

dc.contributor.author Kumara Swamy, K. C.
dc.contributor.author Burton, Sarah D.
dc.contributor.author Holmes, Joan M.
dc.contributor.author Day, Roberta O.
dc.contributor.author Holmes, Robert R.
dc.date.accessioned 2022-03-27T09:59:43Z
dc.date.available 2022-03-27T09:59:43Z
dc.date.issued 1990-05-01
dc.description.abstract X-ray and variable temperature NMR investigations of cyclic pentaoxyphosphoranes reveal a preference of six-and seven-membered rings for apical-equatorial orientations of trigonal bipyramids. Saturated six-membered rings prefer a boat conformation. Apical-equatorial ring pseudorotations are more facile for five-membered rings, whereas ligand exchange via diequatorial ring placement is more facile for the larger rings. Application to enzymatic reactions of cyclic AMP is emphasized. © 1990, Taylor & Francis Group, LLC. All rights reserved.
dc.identifier.citation Phosphorus, Sulfur, and Silicon and the Related Elements. v.49-50(1-4)
dc.identifier.issn 10426507
dc.identifier.uri 10.1080/10426509008038981
dc.identifier.uri http://www.tandfonline.com/doi/abs/10.1080/10426509008038981
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13508
dc.title Cyclic oxyphosphoranes with six-and seven-membered rings
dc.type Journal. Article
dspace.entity.type
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