✦ LIBER ✦

Studies of the elimination of 4-aryl-3-methyl-4-piperidinols—V: Some factors affecting the direction of elimination

✍ Scribed by A.F. Casy; A.H. Beckett; M.a. Iorio

Book ID: 103396164
Publisher: Elsevier Science
Year: 1967
Tongue: French
Weight: 432 KB
Volume: 23
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(67)85095-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Studies of the elimination of 4-aryl-3-m

Studies of the elimination of 4-aryl-3-methyl-4-piperidinols—I : The conformation of epimeric 1-alkyl (and aralkyl)-4-aryl-5-methyl-1,2,5-6-tetrahydropyridine hydrochlorides

✍ A.F. Casy; A.H. Beckett; M.A. Iorio; H.Z. Youssef 📂 Article 📅 1965 🏛 Elsevier Science 🌐 French ⚖ 1022 KB

Syntheses of 2-(chlorinated methyl)-4-me

Syntheses of 2-(chlorinated methyl)-4-methylene-1,3-dioxolanes. Deviations from the predicted direction competitive elimination reactions

✍ Dietrich, Heinz J.; Raynor, Robert J.; Karabinos, Joseph V. 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 573 KB

Synthesis of 1-aryl-3,4-dimethylenepyrro

Synthesis of 1-aryl-3,4-dimethylenepyrrolidines by the thermal elimination of sulfur dioxide

✍ Raphael M. Ottenbrite; Peter V. Alston 📂 Article 📅 1973 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 312 KB

Mechanism of the cycloaddition-eliminati

Mechanism of the cycloaddition-elimination reactions of 4-methyl-5-phenylimino-δ2-1,2,3,4-thiatriazoline with alkyl and aryl isothiocyanates

✍ Gerrit L'Abbé; Karin Buelens 📂 Article 📅 1990 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 339 KB

Steric factors in the kinetically contro

Steric factors in the kinetically controlled direction of elimination of secondary and tertiary esters in the gas phase. The pyrolysis of 4,4-dimethylpent-2-yl acetate

✍ Gabriel Chuchani; Rosa Maria Dominguez 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB

## Abstract The pyrolysis kinetics of 4,4‐dimethylpent‐2‐yl acetate, in a static system and in a vessel seasoned with allyl bromide, have been studied in the temperature range of 300–350°C and the pressure range of 48–211 torr. The olefin products were 4,4‐dimethylpent‐1‐ene, __cis__‐4,4‐dimethylpe

Studies of the elimination of 1,2,-diary

Studies of the elimination of 1,2,-diaryl-4-dimethylaminobutan-2-ols—I : Acid-catalysed eliminations of 1,2-diaryl-4-dimethylamino-3-methylbutan-2-ols and base-catalysed elimination of related 2-chloro derivatives

✍ A.F. Casy; J.L. Myers; P. Pocha 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 626 KB