✦ LIBER ✦

Efficient synthesis of new 1-alkyl(aryl)-5-(3,3,3-trihalo-2-oxopropylidene)-1H-pyrrol-2(5H)-ones

✍ Scribed by Alex F.C. Flores; Lucas Pizzuti; Luciana A. Piovesan; Darlene C. Flores; Juliana L. Malavolta; Claudio M.P. Pereira

Publisher: Elsevier Science
Year: 2010
Tongue: French
Weight: 341 KB
Volume: 51
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2010.07.073

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Effective Synthesis of 5-Aryl-3-ethylide

Effective Synthesis of 5-Aryl-3-ethylidene-3H-pyrrol-2-ones.

✍ A. Yu. Yegorova; I. E. Kamneva; L. S. Shtykova 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

ChemInform Abstract: Synthesis of 5-Amin

ChemInform Abstract: Synthesis of 5-Amino-1-aryl-4- (4-aryl-1,3-thiazol-2-yl)-2,3-dihydro-1H-pyrrol-3-ones.

✍ Yu. M. Volovenko; T. A. Volovnenko; A. V. Tverdokhlebov; I. G. Ryabokon' 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

Synthesis of Arylidine Derivatives of 1-

Synthesis of Arylidine Derivatives of 1-Aryl-3H-pyrrol-2-ones.

✍ A. Yu. Egorova; V. V. Nesterova 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Synthesis of 2-Aryl-5H-[1,3,4]thiadiazol

Synthesis of 2-Aryl-5H-[1,3,4]thiadiazolo[2,3-b]quinazolin-5-ones.

✍ V. N. Britsun; A. N. Esipenko; M. O. Lozinskii 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Bromination of 5-Substituted 3H-Furan-2-

Bromination of 5-Substituted 3H-Furan-2-ones and 3H-Pyrrol-2-ones.

✍ A. Yu. Egorova; V. A. Sedavkina 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 157 KB 👁 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

On 3,5,6-trihalo-2-(pyrrol-2-yl)-1,4-ben

On 3,5,6-trihalo-2-(pyrrol-2-yl)-1,4-benzoquinones

✍ Ribó, Josep M. ;Acero, Carles 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 674 KB

## Abstract In the reaction of pyrroles with tetrahalo‐1,4‐benzoquinones two different processes occur: the oxidation of pyrrole and the coupling reaction to 3,5,6‐trihalo‐2‐(pyrrol‐2‐yl)‐1,4‐benzoquinones. Excess of pyrrole results in doped polypyrrole as the principal reaction product. Excess of