✦ LIBER ✦

Arylation of amines by aryllead triacetates using copper catalysis

✍ Scribed by Derek H.R. Barton; Dervilla M.X. Donnelly; Jean-Pierre Finet; Patrick J. Guiry

Publisher: Elsevier Science
Year: 1989
Tongue: French
Weight: 208 KB
Volume: 30
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)99469-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Phenylation of aromatic and aliphatic am

Phenylation of aromatic and aliphatic amines by phenyllead triacetate using copper catalysis

✍ Derek H.R. Barton; Neerja Yadav-Bhatnagar; Jean-Pierre Finet; Jamal Khamsi 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 170 KB

Amination of aryl halides using copper c

Amination of aryl halides using copper catalysis

✍ Fengrui Lang; Daniel Zewge; Ioannis N Houpis; R.P Volante 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 58 KB

ChemInform Abstract: Amination of Aryl H

ChemInform Abstract: Amination of Aryl Halides Using Copper Catalysis.

✍ Fengrui Lang; Daniel Zewge; Ioannis N. Houpis; R. P. Volante 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Metallic copper catalysis of N-arylation

Metallic copper catalysis of N-arylation of amines by triarylbismuth diacylates

✍ Derek H.R Barton; Jean-Pierre Finet; Jamal Khamsi 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 181 KB

ChemInform Abstract: α-Arylation of Keto

ChemInform Abstract: α-Arylation of Ketones by Aryllead Triacetates. Effect of Methyl and Phenyl Substitution at the α-Position.

✍ J. MORGAN; J. T. PINHEY; B. A. ROWE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Use of the electrophilic c-arylation by

Use of the electrophilic c-arylation by aryllead triacetates in the construction of synthons for aizoaceae and amaryllidaceae alkaloid synthesis

✍ Darren J. Ackland; John T. Pinhey 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 201 KB

The vinylogous 8-keto esters, ethyl 2-methyl-4-oxocyclohex-2-enecarboxylate (Hagemann's Ester) (4), ethyl 4-oxocyclohex-l-enecarboxylate (7a) and its double bond isomer (7b), undergo regiospecific arylation with aryllead triacetates at Cl; reaction of the mixture of isomers ( 7a) and ( 7b) with aryl