Producción Científica Profesorado

Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives



Rojas Lima, Susana

2011

Heraclio López-Ruiz, Horacio Briseño-Ortega, Susana Rojas-Lima, Rosa Santilllán, Norberto Farfán. Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives . Tetrahedron Letters 2011, 52, 4308-4312. DOI: http://dx.doi.org/10.1016/j.tetlet.2011.06.039


Abstract


A novel, one-pot, phenylboronic acid catalyzed, cyanide promoted synthesis of 2-(2-hydroxyphenyl)benzoxazoles from salicylaldehydes and o-aminophenols is described. The synthesis is characterized by mild conditions, short reaction times, and simple workup of crystalline, high purity products.



Producto de Investigación




Artículos relacionados

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

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

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

Structural studies of spiroarsoranes derived from 2-aminophenols

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction

Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes

Synthesis and Study of Monomeric and Dimeric Boronates by Spectroscopic Methods and X-ray Crystallog...

3-Benzoyl-2-isopropyl-4-alkyloxazolidin-5-ones as Efficient and Inexpensive Sources of Enantiopure ?...

Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes

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