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Oxidative degradation of larixol and larixyl acetate

✍ Scribed by Christophe Morin; Nassera Nedjar

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
128 KB
Volume
37
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

The structures and configurations of lar
The structures and configurations of larixol and larixyl acetate
✍ T. Norin; G. Ohloff; B. Willhalm πŸ“‚ Article πŸ“… 1965 πŸ› Elsevier Science 🌐 French βš– 234 KB

From the oleoresin of European larch (Larix europaea D. C. 1 H. Wienhaus et al. (1,Z) isolated a compound which they named larixyl acetate (C22H3603; m.p. 6Za; [a], +67")+. On hydrolysis this compound furnished a diterpenoid diol named larixol (C!2,,H3402; m. p.

Oxidative degradation of polybenzyl
Oxidative degradation of polybenzyl
✍ Robert T. Conley πŸ“‚ Article πŸ“… 1965 πŸ› John Wiley and Sons 🌐 English βš– 497 KB πŸ‘ 1 views

The primary steps involved in the degradation of polybenzyl at temperatures between 140 and 220OC. in the presence of air or pure oxygen has been found to be an attack a t the methylene linkages to give benzhydrol and benzophenone linkages. Kinetic evaluation of the rate of benzophenone-type carbony

Non-oxidative and oxidative alkaline deg
Non-oxidative and oxidative alkaline degradation of pectic acid
✍ Klaus NiemelΓ€; Eero SjΓΆstrΓΆm πŸ“‚ Article πŸ“… 1985 πŸ› Elsevier Science 🌐 English βš– 355 KB

As alkaline degradation products of pectic acid, 6 hydroxymonocarboxylic, 16 dicarboxylic, and 2 tricarboxylic acids were identified by g.l.c.-m.s. as their trimethylsilyl derivatives. In the absence of oxygen, the most abundant degradation products are 3-deoxy-2-C-(hydroxymethyl)pentaric, 2,3\_dide