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Formation and synthetic utility of benzyl- and phenyl-cyclopentadienylthallium

✍ Scribed by Poonam Singh; Marvin D. Rausch; Thomas E. Bitterwolf


Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
858 KB
Volume
352
Category
Article
ISSN
0022-328X

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πŸ“œ SIMILAR VOLUMES


Formation, synthetic utility and structu
✍ D. Alker; A.G. Swanson πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 French βš– 219 KB

The structure of the product obtained by reacting the 1,4-dihydropyridine 6 with pyridinium bromide perbromide has been confirmed by NMR spectroscopy as the I-bromomethyl derivative 7 and its reaction with a range of nucleophiles has been studied.

Electrolysis of phenyl and benzyl quater
✍ M. Finkelstein; R.C. Petersen; S.D. Ross πŸ“‚ Article πŸ“… 1965 πŸ› Elsevier Science 🌐 English βš– 338 KB

Electrolysis of the following salts in various solvents at an aluminum cathode gave benzene as the major cleavage product: trimethylanilinium nitrate, trimethylanilinium methoxide, triethylanilinium nitrate and triethylanilinium methoxide. The rate of formation of benzene was studied in several case