2010
Heraclio López-Ruiz, Horacio Briseño-Ortega, Susana Rojas-Lima, Rosa Santilllán, Norberto Farfán. An efficient potassium cyanide-promoted synthesis of 2-arylbenzoxazoles from [4.3.0]boron heterobycycles. Tetrahedron Letters 2010, Vol. 51, Núm. 19, pp 2633-2635. DOI: http://dx.doi.org/10.1016/j.tetlet.2010.03.027
Abstract
The 2-arylbenzoxazoles 3af were produced in moderate to excellent yields merely by stirring a potassium cyanide (3 equiv)-containing methanol solution of the borobicyclic compounds 1af at room temperature. These compounds were fully characterized spectroscopically [IR, 1H, and 13C NMR and X-ray analysis (3a)] and by elemental analysis.
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.