Publikationen, an denen er mitarbeitet MIGUEL ANGEL YUS ASTIZ (29)

2012

  1. Concise total synthesis and stereochemical analysis of tetraponerines T3 and T4

    Journal of Organic Chemistry, Vol. 77, Núm. 22, pp. 10340-10346

2011

  1. Isoprene-mediated lithiation of imidazole derivatives: Mechanistic considerations

    Arkivoc, Vol. 2011, Núm. 5, pp. 12-22

  2. On the nature of lithium biphenyl in ethereal solvents. A critical analysis unifying DFT calculations, physicochemical data in solution, and a X-ray structure

    Journal of Physical Chemistry B, Vol. 115, Núm. 49, pp. 14610-14616

2009

  1. Structural characterization and bonding properties of lithium naphthalene radical anion, [Li+(TMEDA)2][C10H8˙-], and lithium naphthalene dianion [(Li+TMEDA)2C10H8−2]

    Journal of the Chemical Society. Dalton Transactions, pp. 1286-1289

  2. The reaction of biphenyl radical anion and dianion with alkyl fluorides. From ET to SN2 reaction pathways and synthetic applications

    Tetrahedron, Vol. 65, Núm. 52, pp. 10769-10783

2007

  1. Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: New modes of reactivity of highly reduced organic species in solution

    European Journal of Organic Chemistry, pp. 5514-5526

  2. 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

  3. Reductive dearomatization of biphenyl: sequential one-pot regioselective introduction of two different electrophiles

    Tetrahedron Letters, Vol. 48, Núm. 23, pp. 4105-4109

2006

  1. Reactivity in the upper limits of the reduction potential in solution: arene dianion intermolecular carbolithiation of alkenes

    Tetrahedron Letters, Vol. 47, Núm. 35, pp. 6267-6271

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

1999

  1. N-(α-chloroalkyloxycarbonyl)pyrrolidines as a source of oxygenated d1- reagents

    European Journal of Organic Chemistry, pp. 3005-3012

  2. α-Aminated methyllithium by DTBB-catalysed lithiation of a N- (chloromethyl) carbamate

    Tetrahedron, Vol. 55, Núm. 15, pp. 4831-4842

1997

  1. Chiral lithiomethyl ethers by DTBB-catalyzed chlorine-lithium exchange

    Anales de Quimica, Vol. 93, Núm. 1, pp. 44-48

1996

  1. Lithiomethyl ethyl ether from chloromethyl ethyl ether via a DTBB-catalysed lithiation

    Tetrahedron, Vol. 52, Núm. 5, pp. 1643-1650

  2. N-(chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2- synthon

    Tetrahedron Letters, Vol. 37, Núm. 31, pp. 5593-5596

  3. O-tert-butyl-N-(chloromethyl)-N-methyl carbamate as a source of the MeNHCH2- synthon

    Tetrahedron Letters, Vol. 37, Núm. 31, pp. 5597-5600