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

A practical access to acyl radicals from acyl hydrazides

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

Enantioselective synthesis of ?-amino acids. Part 10: Preparation of novel ?,?- and ?,?-disubstitute...

Highly diastereoselective alkylation, acylation and aldol condensation of cis- and trans-(N-acyloyl)...

Structural studies of spiroarsoranes derived from 2-aminophenols

Synthesis of nitrogen-, oxygen- and sulphur-containing tripodal ligands with a trimethylbenzene core...

Ylidaddukte der Penteltrichloride

Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio

Synthesis of new homochiral 2,3-dialkylpiperazines derived from (R)-(?)-phenylglycinol