MIGUEL ANGEL YUS ASTIZ-rekin lankidetzan egindako argitalpenak (6)

2007

  1. New modes of reactivity in the threshold of the reduction potential in solution. alkylation of lithium PAH (Polycyclic Aromatic Hydrocarbon) dianions by primary fluoroalkanes: A reaction pathway complementing the classical birch reductive alkylation

    Chemistry - A European Journal, Vol. 13, Núm. 36, pp. 10096-10107

2003

  1. Aliphatic organolithiums by fluorine-lithium exchange: n-octyllithium

    Tetrahedron Letters, Vol. 44, Núm. 27, pp. 5025-5027

  2. On the dichotomy of the SN2/ET reaction pathways: An apparent SN2 reactivity in the reaction of naphthalene dianion with alkyl fluorides

    Tetrahedron Letters, Vol. 44, Núm. 6, pp. 1309-1312

  3. Primary alkyl fluorides as regioselective alkylating reagents of lithium arene dianions. Easy prediction of regioselectivity by MO calculations on the dianion

    Tetrahedron Letters, Vol. 44, Núm. 6, pp. 1313-1316

2002

  1. On the mechanism of arene-catalyzed lithiation: The role of arene dianions - Naphthalene radical anion versus naphthalene dianion

    Chemistry - A European Journal, Vol. 8, Núm. 11, pp. 2574-2584

2001

  1. On the mechanism of the naphthalene-catalysed lithiation: The role of the naphthalene dianion

    Tetrahedron Letters, Vol. 42, Núm. 20, pp. 3455-3458