Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Ruthenium-catalyzed alkylation of oxindole with alcohols.

Literature DB >> 19371090

Ruthenium-catalyzed alkylation of oxindole with alcohols.

Abstract

An atom-economical and solvent-free catalytic procedure for the mono-3-alkylation of oxindole with alcohols is described. The reaction is mediated by the in situ generated catalyst from RuCl(3) x xH(2)O and PPh(3) in the presence of sodium hydroxide. The reactions proceed in good to excellent yields with a wide range of aromatic, heteroaromatic, and aliphatic alcohols.

Entities: Chemical

Mesh：

Substances：

Year: 2009 PMID： 19371090 DOI： 10.1021/jo900341w

Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354

Keyword Cloud
Cited

4 in total

1. Cytotoxic activities of substituted 3-(3,4,5-trimethoxybenzylidene)-1,3-dihydroindol-2-ones and studies on their mechanisms of action.

Authors: Aldo Andreani; Massimiliano Granaiola; Alessandra Locatelli; Rita Morigi; Mirella Rambaldi; Lucilla Varoli; Francesco Vieceli Dalla Sega; Cecilia Prata; Tam L Nguyen; Ruoli Bai; Ernest Hamel
Journal: Eur J Med Chem Date: 2013-04-03 Impact factor: 6.514

Ruthenium-catalyzed alkylation of oxindole with alcohols.

1. Cytotoxic activities of substituted 3-(3,4,5-trimethoxybenzylidene)-1,3-dihydroindol-2-ones and studies on their mechanisms of action.

2. A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols.

3. Manganese-Catalyzed α-Alkylation of Ketones, Esters, and Amides Using Alcohols.

4. Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles with Alcohols.