✦ LIBER ✦

Mechanism of the neutral hydrolysis of 1-acyl-1,2,4-triazoles a proton inventory study

✍ Scribed by Willem Karzijn; Jan B.F.N. Engberts

Publisher: Elsevier Science
Year: 1978
Tongue: French
Weight: 235 KB
Volume: 19
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(78)80044-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Thermal Rearrangement of 4-Alkyl-4H-1,2,

Thermal Rearrangement of 4-Alkyl-4H-1,2,4-triazoles to 1-Alkyl-1H-1,2,4-triazoles − A Study of the Mechanism by Cross-over Experiments

✍ Odd R. Gautun; Per H. J. Carlsen 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 230 KB 👁 1 views

An analysis of complex alkyl-substituent

An analysis of complex alkyl-substituent effects in the water-catalyzed hydrolysis of 1-acyl-1,2,4-triazoles

✍ Herman J. Mooij; Jan B. F. N. Engberts; Marvin Charton 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 483 KB

Water- and hydroxide-ion-catalyzed hydro

Water- and hydroxide-ion-catalyzed hydrolysis of 1-acyl-1,2,4-triazoles in mixed aqueous solvents. The effect of substrate hydrophobicity

✍ Willem Karzijn; Jan. B. F. N. Engberts 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 341 KB

Study of 6-hydrazinophenathridine in acy

Study of 6-hydrazinophenathridine in acylation and annelation reactions of the 1,2,4-triazole ring

✍ A. G. Mikhailovskii 📂 Article 📅 1998 🏛 Springer US 🌐 English ⚖ 194 KB

ChemInform Abstract: The Acylation of 4-

ChemInform Abstract: The Acylation of 4-Amino-4,5-dihydro-1H-1,2,4-triazol-5-ones.

✍ Aysun Ikizler; Nese Dogan; Aykut A. Ikizler 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

A kinetic study of the thermolysis of N-

A kinetic study of the thermolysis of N-crotyl substituted 1,2,4-triazoles

✍ Per H. J. Carlsen; Kåre B. Jørgensen 📂 Article 📅 2000 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 291 KB

## Abstract A kinetic study of the thermolysis of 4‐crotyl‐3,5‐diphenyl‐4__H__‐1,2,4‐triazole (**1**) in a melt of the neat compound was performed at temperatures in the range of 260–350 °C. The main products formed were 1‐crotyl‐3,5‐diphenyl‐1__H__‐1,2,4‐triazole (3) and 1‐(1‐methylallyl)‐3,5‐diph