Producción Científica Profesorado

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



Rojas Lima, Susana

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.



Producto de Investigación




Artículos relacionados

Structure-Activity Relationships for Inhibition of Cysteine Protease Activity and Development of Pla...

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

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

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

X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone

Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters

Further insight into three center hydrogen bonding. Participation in tautomeric equilibria of hetero...

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction

A flexible access to highly functionalised boronates

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