𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Tracer studies on the mechanism of the dienone-pheno; rearrangement with mineral acids

✍ Scribed by R. Futaki

Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
36 KB
Volume
9
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

IHOd -Hogfjp 2458

VI under the last figure should read IV'.

πŸ“œ SIMILAR VOLUMES

On the mechanism of the dienone-phenol r
On the mechanism of the dienone-phenol rearrangement of A 2-methyl-1,4-dien-3-one
✍ Paul J. Kropp πŸ“‚ Article πŸ“… 1963 πŸ› Elsevier Science 🌐 French βš– 224 KB

IT ia well known that croae-conjugated cyclohexadienonee type I rearrange on treatment with aqueoue mineral acids cillcinnsti, Ohio of the general toamlrtureof two phenollc products, types III and VI. 1,2 Evidence has been presented that the formation of the tetrehydro-l-naphthol derivativea (type I

Studies on the mechanism of sesquiterpen
Studies on the mechanism of sesquiterpene biosynthesis humulene-germacrene rearrangement
✍ Akira Itoh; Hitosi Nozaki; Hisashi Yamamoto πŸ“‚ Article πŸ“… 1978 πŸ› Elsevier Science 🌐 French βš– 243 KB

Cations la, E, &, and E are presumed to be the key intermediates in the enzymic cyclization of farnesyl pyrophosphate and the starting points for the intricate series of cyclization and rearrangement steps which lead to a variety of polycyclic sesquiterpenes. 1 Despite considerable speculation, 2 th