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Deuterium isotope effects in the meta photocycloaddition of aromatic compounds to alkenes

✍ Scribed by P. de Vaal; G. Lodder; J. Cornelisse


Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
258 KB
Volume
26
Category
Article
ISSN
0040-4039

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✦ Synopsis


Secondary deuterium isotope effects were observed in the meta photocycloaddition


πŸ“œ SIMILAR VOLUMES


Intramolecular deuterium isotope effects
✍ P. de Vaal; G. Lodder; J. Cornelisse πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 French βš– 334 KB

The effect of substitution of hydrogen by deuterium in some aromatic compounds on product distributions in the meta photocycloaddition to al kenes was investigated. The isotope effects found are in agreement with a polar mechanism.

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PHENYL trifluoromethyl carbinols are oxidized by aqueous alkaline permsnganate to the corresponding ketones. We wish to report a kinetic isotope effect of unusual size for the reaction of the 1-deuterio analogs of these compounds. YC6H4CDOHCF3 + 2Mn04-+ 2OH-4 YC H COCF3 + 2Mn0 \* + H20 + RDO 64 4 1-

Intrinsic deuterium isotope effects of d
✍ Hartmut H. Balzer; Stefan Berger πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 404 KB

## Abstract The ^3^Δ‐deuterium isotope effects of partially and fully deuteriated __tert__‐butyl groups on the ^13^C NMR spectra of __tert__‐butylbenzene and derivatives are discussed in detail. It is shown that they correlate with the chemical shift of C‐1 of the aromatic ring. It has been demonst