Formation of a cyclic hemiketal from the chromic acid oxidation of a tricyclic hydrocarbon
β Scribed by D.C. Kleinfelter; R.W. Aaron; W.E. Wilde; T.B. Bennett Jr.; H. Wei; J.E. Wiechert
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 195 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Berson(1) has noted that there is only a relatively small group of reactions involving
π SIMILAR VOLUMES
iioriiinl hns now t o be cntered for inirnediiitcly results in the eliininntion of n niintber of pliistics nuide froni low nielt ing point, coiiipoiwits, s!ich iis those eniploying wnses, pitches, sliellacs, etc. , Undcr this c1;issificntion tile perforninnce of n pliistic is corupliciitcd 11y the c
The ruthenium tetroxide oxidation of cyclic N-acyl amines by a 10% NaIO 4 aqueous solution containing tert-butanol as a single layer system resulted in the endo-cyclic C-N bond cleavage to afford the x-amino acids as almost sole products in good yields, while a similar oxidation under the double lay
## Abstract In aqueous H~2~SO~4~ media, chromic acid oxidation of hexitols (Dβsorbitol and Dβmannitol) to their corresponding aldohexoses in presence and absence of 2,2β²βbipyridyl (bipy) have been studied under the experimental conditions, [hexitols]~T~ β« [Cr(VI)]~T~ and [bipy]~T~ β« [Cr(VI)]~T~ (su