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Haloacetylated enol ethers. 14 [6]. Reaction of β-alkoxyvinyl trifluoromethyl ketones with N-methylhydroxylamine

✍ Scribed by Marcos A. P. Martins; Alex F. C. Flores; Giovani P. Bastos; Nilo Zanatta; Helio G. Bonacorso


Publisher
Journal of Heterocyclic Chemistry
Year
1999
Tongue
English
Weight
289 KB
Volume
36
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

The reaction of a series of β‐methoxyvinyl trifluoromethyl ketones [CF~3~COC(R^2^)C(OMe)R^1^, where R^1^ = Me, ‐(CH~2~)~3~‐__C__3, ‐CH~2~)~4~‐__C__3, Ph and R^2^ = H, Me, ‐(CH~2~)~3~‐__C__4, ‐(CH~2~)~4~‐__C__4] with N‐methylhydroxylamine is reported. The regiochemistry of the reaction are explained by MO calculation data.


📜 SIMILAR VOLUMES


Haloacetylated enol ethers. 8 [12]. Reac
✍ Nilo Zanatta; Maria de F. M. Cortelini; Marcos J. S. Carpes; Helio G. Bonacorso; 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 309 KB

## Abstract In this work the results of the reaction of β‐alkoxyvinyl trihalomethyl ketones 1, 2a‐e, with guanidine hydrochloride are reported. Depending on the ketone 1 or 2 and the conditions under which the reactions were carried out, 4‐trihalomethyl‐2‐amino pyrimidines, β‐alkoxyvinyl carboxylic

Haloacetylated enol ethers: 15. Study of
✍ Nilo Zanatta; Claudia Da C. Madruga; Patricia Da C. Marisco; Darlene C. Flores; 📂 Article 📅 2000 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 344 KB

## Abstract A study of the regiochemistry of the cyclo‐condensation reaction of ß‐alkoxyvinyl trihalomethyl ketones with an unsymmetric dinucleophile __N__‐methyl thiourea to afford a series of 1‐methyl‐3‐(4,4,4‐trifluoro[chloro]‐3‐oxo‐1‐butenyl)thioureas and the corresponding __N__‐methyl pyrimidi