Publicaciones en las que colabora con Enrique Teso Vilar (48)

2013

  1. Electron ionization-induced fragmentation of bridgehead-substituted norbornan-2-ones derived from fenchone

    International Journal of Mass Spectrometry, Vol. 334, pp. 49-57

2012

  1. Water-trapping of unstable carbocations taking place into the inverted region of the Marcus equation. First experimental and computational evidence

    Tetrahedron, Vol. 68, Núm. 13, pp. 2892-2898

2008

  1. Solvent and stereoelectronic effects on the solvolysis rates of oxaspirocyclopropanated 1-norbornyl triflates and related bridgehead derivatives

    Journal of Organic Chemistry, Vol. 73, Núm. 17, pp. 6607-6614

2007

  1. First efficient synthesis of enantiopure homoketopinic acid

    Letters in Organic Chemistry, Vol. 4, Núm. 2, pp. 123-125

2006

  1. A novel modification of the Ritter reaction: stereoselective synthesis of bridgehead-fused Δ2-norbornanethiazolines from thiocamphor and thiofenchone

    Tetrahedron Asymmetry, Vol. 17, Núm. 21, pp. 2970-2975

  2. Density functional theory study of self-association of N-methylformamide and its effect on intramolecular and intermolecular geometrical parameters and the cis/trans population

    Journal of Chemical Physics, Vol. 124, Núm. 23

2005

  1. A new type of anomalous ozonolysis in strained allylic bicycloalkan-1-ols

    Tetrahedron Letters, Vol. 46, Núm. 31, pp. 5157-5159

  2. Electron ionization mass spectral studies of bridgehead 7,7-dimethylnorbornane-based β-amino alcohols

    Rapid Communications in Mass Spectrometry, Vol. 19, Núm. 8, pp. 1005-1010

  3. Enantiospecific access to 10-N-substituted camphors

    Tetrahedron, Vol. 61, Núm. 3, pp. 599-601

  4. Palladium(II)-catalyzed ring expansion of a 1-alkenyl cyclopentanol

    Tetrahedron Letters, Vol. 46, Núm. 20, pp. 3509-3511

  5. Stereocontrolled synthesis of conformationally restricted enantiopure triols and dihydroxy acids based on the norbornane framework

    Tetrahedron Asymmetry, Vol. 16, Núm. 13, pp. 2329-2332

2004

  1. 2-exo- versus 2-endo-Hydroxyl in δ-amino norbornan-2-ol-based catalysts: Investigating the role of the C(2) configuration in the asymmetric induction

    Tetrahedron Asymmetry, Vol. 15, Núm. 5, pp. 753-756

  2. A short and convenient procedure for the stereoselective synthesis of 2-hydroxy-1-norbornanesulfonamides

    Tetrahedron Asymmetry, Vol. 15, Núm. 2, pp. 293-298

  3. Intramolecular-activation evidence for the unexpected Beckmann fragmentation of C(1)-substituted-7-bromonorbornane-2-ones

    Tetrahedron, Vol. 60, Núm. 42, pp. 9447-9451

2003

  1. About the Leuckart reaction of chiral 2-norbornanones bearing electron-withdrawing groups: Reaction of bridgehead triflates and triflamides

    Tetrahedron, Vol. 59, Núm. 9, pp. 1565-1569

  2. First access to enantiopure C(7)-substituted fenchones: New norbornane-based chiral materials from the chiral pool

    Tetrahedron Asymmetry, Vol. 14, Núm. 12, pp. 1607-1609

  3. Synthesis and catalytic activity of 10-(aminomethyl)isoborneol-based catalysts: The role of the C(2)-group on the asymmetric induction

    Tetrahedron Asymmetry, Vol. 14, Núm. 14, pp. 1959-1963

2002

  1. A new enantiospecific synthetic procedure to the taxoid-intermediate 10-methylenecamphor, and 10-methylenefenchone

    Tetrahedron Asymmetry, Vol. 13, Núm. 1, pp. 17-19

  2. A novel and simple procedure for the enantiospecific synthesis of bridgehead norbornane thioethers and thiocyanates

    Tetrahedron Asymmetry, Vol. 13, Núm. 24, pp. 2635-2639

  3. A novel enantiospecific route to 10-hydroxyfenchone: A convenient intermediate for C(10)-O-substituted fenchones

    Tetrahedron Asymmetry, Vol. 12, Núm. 24, pp. 3325-3327