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

r-Alkylation of (S)-Asparagine with Self-Regeneration of the Stereogenic Center: Enantioselective Sy...

Phenylmethyl 2,3,4-tri-O-acetyl--D-fucopyranoside

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

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

A practical access to acyl radicals from acyl hydrazides

Effect of TiO2Al2O3 SolGel Supports on the Superficial Ni and Mo Species in Oxidized and Sulfided Ni...

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio

Comparative Structural Characterization of the Biquaternized N-CH3 and N-BH3 Derivatives of the cis-...

Synthesis of New Chiral Derivatives of N,N?-Dimethylpropyleneurea (DMPU) and Examination of Their In...

An efficient potassium cyanide-promoted synthesis of 2-arylbenzoxazoles from [4.3.0]boron heterobicy...