Directed Ring-Opening Of 1,5-Dioxaspiro[3.2]Hexanes: Selective Formation Of 2,2-Disubstituted Oxetanes
Document Type
Article
Publication Date
2-21-2003
Published In
Journal Of Organic Chemistry
Abstract
1,5-Dioxaspiro[3.2]hexanes undergo ring-opening reactions with many heteroatom nucleophiles to provide alpha-substituted-beta'-hydroxy ketones. However, certain Lewis acidic nucleophiles provide 2,2-disubstituted oxetanes. Herein, the results of reactions of 3-phenyl-1,5-dioxaspiro[3.2]hexane with a variety of nitrogen-containing heteroaromatic bases are reported. There appears to be a correlation between the pK(a) of the nucleophile and the reaction outcome with more acidic nucleophiles providing 2,2-disubstituted oxetanes. Moreover, the mode of ring opening can be directed toward the substituted oxetane by the addition of a Lewis acid. These results are rationalized by calculation of stationary points on the potential energy surfaces for the various possible reaction pathways using ab initio molecular orbital methods.
Recommended Citation
R. Taboada, G. G. Ordonio, A. J. Ndakala, A. R. Howell, and Paul R. Rablen.
(2003).
"Directed Ring-Opening Of 1,5-Dioxaspiro[3.2]Hexanes: Selective Formation Of 2,2-Disubstituted Oxetanes".
Journal Of Organic Chemistry.
Volume 68,
Issue 4.
1480-1488.
DOI: 10.1021/jo0206465
https://works.swarthmore.edu/fac-chemistry/83