Ring Opening of 1,5-Dioxaspiro[3.2]hexanes: Selective Preparation of α-Heterofunctionalized-β‘-hydroxy Ketones or 2,2-Disubstituted Oxetanes
- 31 August 1999
- journal article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (6) , 825-827
- https://doi.org/10.1021/ol990039c
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The First General Synthesis of 1,5-Dioxaspiro[3.2]hexanesThe Journal of Organic Chemistry, 1998
- Easy availability of more concentrated and versatile dimethyldioxirane solutionsTetrahedron Letters, 1996
- Asymmetric Epoxidation of Allylic Alcohols: the Katsuki–Sharpless Epoxidation ReactionPublished by Wiley ,1996
- A Versatile Preparation of 2-MethyleneoxetanesThe Journal of Organic Chemistry, 1996
- Catalytic asymmetric oxidations using optically active (salen)manganese(III) complexes as catalystsCoordination Chemistry Reviews, 1995
- Highly diastereoselective acetal cleavages using novel reagents prepared from organoaluminum and pentafluorophenolJournal of the American Chemical Society, 1993
- 1,4-Dioxaspiro[2.2]pentanes. Synthesis, spectroscopic properties, and reactions with nucleophilesThe Journal of Organic Chemistry, 1991
- Epoxidation of 3,6-di-tert-butyl-2,2,7,7-tetramethyl-3,4,5-octatriene. Isolation of a stable methylenecyclopropanoneJournal of the American Chemical Society, 1987
- Effect of central substituents on the gas-phase acidities of propenesThe Journal of Organic Chemistry, 1984
- Mechanism of the Thermal Isomerization of Some Diels-Alder Adducts of 1,4-Benzoquinone 2,3-EpoxidesJournal of the American Chemical Society, 1966