𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The structure of skatole dimer. New reactions of indoline derivatives

✍ Scribed by Giancarlo Berti; Antonio Da Settimo; Domenico Segnini


Book ID
104249885
Publisher
Elsevier Science
Year
1960
Tongue
French
Weight
267 KB
Volume
1
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


111 oonneotion with our work on the determination of the baee rtrengtho of indole derivatives,' It became of lmportanee to study the dlmere whloh some of thee8 oompounde form in acldlo eolutlone. While strtaottare I was deflnltely proved for lndolo dlmer,* no reoent data were available on ekatole direr, althou@ Its rtructure had been 8 oatter of dispute between 0ddo,3 who proposed a pentaoyollo formula, and Sehalt%-DulJlont,4 who favoured Instead the more likely formulation II, but did not give a real proof for It. A rrtruoture mlmilar to that of dllndole (I) was evidently lapoeelble for dlakatole, but III eeemed to be a poeslble alternative for II, on the baela of our remalte on the oomparatire borrloltlee of lndole and Its me-1 derIvatIvea.' We have now euooeeded In prorlng that III le the atruoture of dlekatole. In a reoent paper Bo-


πŸ“œ SIMILAR VOLUMES


Analysis of dimeric species derived from
✍ Mary R. Roth; Fred L. Smardo Jr.; Ruth Welti πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 English βš– 722 KB

Phosphatidylethanolamines of various fatty acyl species in vortexed lipid dispersions were reacted with dimetbylsuberimidate to produce dimeric products. The yield was 34% at pH 10 and 2% at pH 7. The crosslinked phosphatidylethanolamine species were separated from minor products and the reactants b