Structure−Reactivity Relationships for Associative Displacement Reactions of Penta- and Hexacoordinate Cyclic Oxyphosphoranes with Catechols1,2
Author:
Affiliation:
1. Department of Chemistry, Box 34510, University of Massachusetts, Amherst, Massachusetts 01003
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic970919s
Reference55 articles.
1. Hexacoordination via Sulfur Donor Action in Bicyclic Pentaoxyphosphoranes1
2. Presented in part at the 211th National Meeting of the American Chemical Society, New Orleans, LA, March 24−28, 1996; INOR 189.
3. Thatcher, G. R. J.; Kluger, R.AdvancesinPhysicalOrganicChemistry; Bethell, D., Ed.; Academic Press: New York, 1989; Vol. 25, pp 99−265 and references cited therein.
4. Pseudo-rotation in the hydrolysis of phosphate esters
5. The enthalpies of hydrolysis of acyclic, monocyclic, and glycoside cyclic phosphate diesters.
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