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Lead tetraacetate oxidation of unsaturated alcohols. Oxide formation and fragmentation

✍ Scribed by Robert M. Moriarty; Kishori Kapadia

Publisher
Elsevier Science
Year
1964
Tongue
French
Weight
244 KB
Volume
5
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

Lead tetraacetate oxidation of cycloocta
Lead tetraacetate oxidation of cyclooctanol. Transannular oxide formation.
✍ Robert M. Moriarty; Harold G. Walsh πŸ“‚ Article πŸ“… 1965 πŸ› Elsevier Science 🌐 French βš– 187 KB

## Lead tetmacetate oxidation of monohydric aIdloIs bearing a carbon-hydrogen bond in the 8 -position represents a valuable synthetic route to tetmhydrofurane derivatives l,2.

Lead tetraacetate oxidation of bridged b
Lead tetraacetate oxidation of bridged bicyclic alcohols
✍ Keizo Kitahonoki; Akio Matsuura πŸ“‚ Article πŸ“… 1964 πŸ› Elsevier Science 🌐 French βš– 165 KB

IN recent years, the oxidation of monohydric alcohols to tetrohydrofuran derivatives by lead tetraacetate has been studied extensively in steroids and used successfully to functionalize the "unactivated" Cl\* or Ctp angular methyl group (1,2). We have applied this type of reaction in the bridged rin

Lead tetraacetate oxidation of ketoximes
Lead tetraacetate oxidation of ketoximes and aldoximes
✍ G. Just; K. Dahl πŸ“‚ Article πŸ“… 1966 πŸ› Elsevier Science 🌐 French βš– 271 KB

Oxidation of aliphatic ketoximes (1) and aldoximes (2) by lead tetraacetate (Pb(OAcjq) has been reported to lead to unstable geminal nitrosoacetates and to dimeric nitrosoacetates, respectively, while a,S-unsaturated and arylaldoximes afforded oxime anhydride N-oxides and carbonyl compounds (3).

Allylic Oxidation of some 5,6-Unsaturate
Allylic Oxidation of some 5,6-Unsaturated Steroids with Lead Tetraacetate. Communication XXII on reactions with lead tetraacetate
✍ M. StefanoviΔ‡; A. JokiΔ‡; Z. MaksimoviΔ‡; Lj. Lorenc; M. Lj. MihailoviΔ‡ πŸ“‚ Article πŸ“… 1970 πŸ› John Wiley and Sons 🌐 German βš– 600 KB

Es konnte noch 1 pg Hg neben 150 pg eines Gemisches vieler Kationen mit einer Genauigkeit von f 4% bestimmt werden. Erfassungsgrenze und Fehlerbreite waren weitgehend durch den Neutronenfluss des zur Verfiigung stehenden Kernreaktors des Physikalischen Instituts der Universitat Base1 gegeben.