✦ LIBER ✦

Rhodium-Catalyzed Hydroformylation of 2-Vinyl- and 3-Vinyl-1-tosylpyrroles As a Convenient Synthetic Route to the Corresponding 2-(1-Tosylpyrrolyl)propanals and Derivatives

✍ Scribed by Settambolo, Roberta; Caiazzo, Aldo; Lazzaroni, Raffaello

Book ID: 126990006
Publisher: Taylor and Francis Group
Year: 1997
Tongue: English
Weight: 331 KB
Volume: 27
Category: Article
ISSN: 0039-7911
DOI: 10.1080/00397919708005459

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Rhodium-Catalyzed H

ChemInform Abstract: Rhodium-Catalyzed Hydroformylation of 2-Vinyl- and 3-Vinyl-1-tosylpyrroles as a Convenient Synthetic Route to the Corresponding 2-(1-Tosylpyrrolyl)propanals and Derivatives

✍ R. SETTAMBOLO; A. CAIAZZO; R. LAZZARONI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

ChemInform Abstract: A Novel and Effecti

ChemInform Abstract: A Novel and Effective Route to 1,3-Oxazolidine Derivatives. Palladium-Catalyzed Regioselective [3 + 2] Cycloaddition of Vinylic Oxiranes with Imines.

✍ Jae-Goo Shim; Yoshinori Yamamoto 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

A Novel and Effective Route to 1,3-Oxazolidine Derivatives. Palladium-Catalyzed Regioselective [3 + 2] Cycloaddition of Vinylic Oxiranes with Imines. -The present palladium-catalyzed intermolecular regioselective [3 + 2] cycloaddition of imines (I) with vinylic oxiranes (II) is a new version of 1,3

Rhodium(II) acetate-catalyzed reaction o

Rhodium(II) acetate-catalyzed reaction of ethyl 2-diazo-3-oxopent-4-enoates: Simple routes to 4-aryl-2-hydroxy-1-naphthoates and β,β-unsaturated esters. The dianion of ethyl 4-(diethylphosphono)acetoacetate as a propionate homoenolate equivalent

✍ Edward C. Taylor; Huw M.L. Davies 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 170 KB

Rhodium(I1) acetate-catalyzed decomposition of ethyl 2-diazo-3oxopent-4-enoates results in the formation of either 4-aryl-2-hydroxynaphthoates or 6,y-unsaturated esters. In the latter transformation, the dianion of 4-(diethylphosphono)acetoacetate functions as a propionate homoenolate equivalent.