Producción Científica Profesorado

Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes



Rojas Lima, Susana

2007

Juan Pablo, García-Merinos, Juan Pablo Hernández-Pérez, Leonel Martínez-García, Susana Rojas-Lima, Heraclio López Ruiz. Et3, and efficient Mediattoo for Xanthate Transfer Based Radical Processes. Journal of the Mexican Chemical Society, 51(4), 209-212.(2007). ISSN 1870-249X


Abstract


The triethylborane mediated intermolecular addition of diverse carbon radicals, derived from the corresponding xanthates, to allyl acetate (10b) and 4-allyl-1,2-dimethoxybenzene (10a) was studied in various solvents. In most cases, the product yields in water at room temperature were as good as, or better than, those obtained using 1,2-dichloroethane as the solvent. In contrast, ethanol in most cases was not a useful solvent in which to conduct these reactions.



Producto de Investigación




Artículos relacionados

Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.

Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition

Preparation of Seven- and Eight-Membered Boron Heterocycles from Different Salen Ligands and Arylbor...

Cathepsins X and B Can Be Differentiated through Their Respective Mono- and Dipeptidyl Carboxypeptid...

Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates

Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols

Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes

O-benzyl-N-(2-furoyl)thiocarbamate

Synthesis and Study of Isomeric Benzo[1,4]oxazines and Benzothiazolines by NMR Spectroscopy and X-Ra...

Enantioselective synthesis of ?-amino acids. Part 11: Diastereoselective alkylation of chiral deriva...