| dc.contributor.author | J, Ndakala Albert | |
| dc.contributor.author | R, Howell Amy | |
| dc.date.accessioned | 2013-05-30T15:33:14Z | |
| dc.date.available | 2013-05-30T15:33:14Z | |
| dc.date.issued | 1999 | |
| dc.identifier.citation | Ring Opening of 1,5-Dioxaspiro[3.2]hexanes: Selective Preparation of alpha-Heterofunctionalized- beta'-hydroxy Ketones or 2,2-Disubstituted Oxetanes, Howell, Amy R., and Ndakala Albert J. , Organic Letters, Volume 1, p.825-827, (1999) copy at http://profiles.uonbi.ac.ke/andakala/publications/ring-opening-15-dioxaspiro32hexanes-selective-preparation-heterofunctionalized | en |
| dc.identifier.uri | http://pubs.acs.org/doi/abs/10.1021/ol990039c | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/27933 | |
| dc.description.abstract | Abstract.................................. Image
2-Methyleneoxetanes have been converted into 1,5-dioxaspiro[3.2]hexanes with dimethyldioxirane. Reaction of the dioxaspirohexanes with a range of heteroatom nucleophiles, hydride donors, or organoaluminum reagents was successful under neutral or mild conditions, affording, selectively, polyfunctionalized ketones or 2,2-disubstituted oxetanes. | |
| dc.language.iso | en | en |
| dc.title | Ring Opening of 1,5-Dioxaspiro[3.2]hexanes: Selective Preparation of alpha-Heterofunctionalized- beta'-hydroxy Ketones or 2,2-Disubstituted Oxetanes | en |
| dc.type | Article | en |
| local.publisher | Department of Chemistry | en |
