✦ LIBER ✦

Reactions of 2,3-diferrocenylcyclopropenone with methyllithium and phenyllithium

✍ Scribed by Elena I Klimova; Tatiana Klimova; Simón Hernández Ortega; Marı́ana Esquivelzeta Rabell; Lena Ruı́z Ramı́rez; Marcos Martı́nez Garcı́a

Book ID: 108187839
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 299 KB
Volume: 689
Category: Article
ISSN: 0022-328X
DOI: 10.1016/j.jorganchem.2004.03.045

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

2,3-Diferrocenylcyclopropenone in the re

2,3-Diferrocenylcyclopropenone in the reaction with organomagnesium compounds

✍ E. I. Klimova; T. Klimova; L. Ruiz Ramirez; J. M. Mendez Stivalet; S. Hernandez 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 541 KB

2,3-Diferrocenylcyclopropenone (III) in

2,3-Diferrocenylcyclopropenone (III) in the Reaction with Organomagnesium Compounds.

✍ E. I. Klimova; T. Klimova; L. Ruiz Ramirez; J. M. Mendez Stivalet; S. Hernandez 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 148 KB

The Reaction of 2,3-Dichloro-p-dioxane w

The Reaction of 2,3-Dichloro-p-dioxane with Phenyllithium

✍ Summerbell, R. K.; Smedley, William M.; Jerina, Donald M.; Berger, Daniel R. 📂 Article 📅 1962 🏛 American Chemical Society 🌐 English ⚖ 383 KB

Reaction of phenyllithium with 1-halo-2-

Reaction of phenyllithium with 1-halo-2-butenes

✍ Wawzonek, Stanley; Studnicka, Benedict J.; Zigman, Alvin R. 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 459 KB

Reaction of 4-Ethoxy-2-(2,3,3-trichloro-

Reaction of 4-Ethoxy-2-(2,3,3-trichloro-1-nitro- 2-propenylidene)benzazetine with Methyl- and Phenyllithium

✍ V. I. Potkin; V. A. Knizhnikov; A. A. Yanuchok; R. V. Kaberdin 📂 Article 📅 2001 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 40 KB

The reaction of 2-chlorobicyclo[2.2.1]he

The reaction of 2-chlorobicyclo[2.2.1]heptene with methyllithium

✍ Paul G. Gassman; Thomas J. Atkins 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 172 KB

The reaction of methyllithium with 2-chlorobicyclo[2.2.1]heptene (j,) has been reported to produce P-methylbicyclo[2.2.l]heptene (x) in 73% yield.2 This appeared to be a unique example of a substitution of a vinylic chloride by an alkyl group through reaction with an organolithium reagent. Whereas,