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.
X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles