2011
Villanueva-García Fabián, Reyes Priscilla, Keith H. Pannell, Álvarez-Hernández Alejandro , Valois Ismael, Juárez-Ruiz Juan M., Flores-Rizo Juan O., and Peña-Cabrera Eduardo. Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters. ARKIVOC 2011, (ix) 105-124. Arkat USA. Estados Unidos.
Abstract
The reactivity of squarylferrocenes was studied in the addition of several N-centered nucleophiles. A total of seven simple amines (primary and secondary) were added to both monosquarylferrocene and 1,1?-bissquarylferrocene to generate 14 ferrocenylsquaramides in 85-98%. Likewise, five aminoesters were added to the same scaffolds to produce a novel family of 10 ferrocene-aminoester conjugates in good to excellent yields (57-95%).
Phenylmethyl 2,3,4-tri-O-acetyl--D-fucopyranoside
A flexible access to highly functionalised boronates
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
A practical access to acyl radicals from acyl hydrazides
X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone