๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Mechanisms of addition -1; The addition of bromine and bromine acetate to some para-substituted cinnamates in acetic acid

โœ Scribed by Michael A. Wilson


Publisher
Elsevier Science
Year
1975
Tongue
French
Weight
175 KB
Volume
16
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Mechanism of the oxidation of para-subst
โœ Ayano Sakai; David G. Hendrickson; William H. Hendrickson ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 143 KB

The ฯ-value of -1.8 for the oxidation of para-substituted 1-phenylethanols by sodium hypochlorite in acetic acid suggests that ketone is formed directly from alcohol by loss of a hydride. The kinetic isotope effect is 3.0. When the disappearance of oxidant is followed by iodometric titration, 5-nona

Novel regiospecificity in the acid-catal
โœ M.A. Battiste; J.M. Coxon; R. Edelman ๐Ÿ“‚ Article ๐Ÿ“… 1972 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 170 KB

We report a striking example of unprecedented regiospecificity in the addition of acetic acid to endo-tricyclo[3.2.1.0z"]oct-6-ene (1). The addition proceeds with surprising ease in acetic acid at 80' (3 days) or at room temperature in the presence of catalytic amounts of toluenesulphonic acid to yi