Publicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (25)

2010

  1. The role of the C(2) configuration and methyl substitution on the catalytic activity of novel 2,3,3- and 2,7,7-trimethyl-substituted γ- aminonorbornan-2-ols

    Chirality, Vol. 22, Núm. 8, pp. 778-787

2009

  1. Electron ionisation mass spectral studies of bridgehead-fused δ2-norbornanethiazolines

    Rapid Communications in Mass Spectrometry, Vol. 23, Núm. 6, pp. 856-862

2008

  1. Highly active ethylene/hydroxyl comonomers copolymerization using metallocene catalysts

    Journal of Applied Polymer Science, Vol. 109, Núm. 3, pp. 1529-1534

2007

  1. First efficient synthesis of enantiopure homoketopinic acid

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

  2. Surprising obtention of an enantiopure eight-membered cyclic ether from camphor

    Tetrahedron Letters, Vol. 48, Núm. 30, pp. 5185-5188

  3. The role of conformational flexibility on the catalytic activity of norbornane-derived β-, γ- and δ-amino alcohols

    Tetrahedron Asymmetry, Vol. 18, Núm. 6, pp. 742-749

  4. Unexpected reactivity of 1-amine-2-methylenenorbornane hydrochlorides with m-CPBA

    Tetrahedron Letters, Vol. 48, Núm. 34, pp. 5981-5983

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

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

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

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

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

2002

  1. The role of the substitution pattern on the catalytic activity of chiral bridgehead norbornane-derived β-amino alcohols

    Tetrahedron Asymmetry, Vol. 13, Núm. 14, pp. 1457-1460

  2. Unexpected bromine-assisted Beckmann fragmentation of a C1-electron-acceptor substituted 7-bromonorbornan-2-one upon hydroxylamine treatment

    European Journal of Organic Chemistry, pp. 781-783

2001

  1. A new convenient procedure for the preparation of enantiopure C10-S- and C10-Se-substituted camphor-derived sulfides and selenides

    Tetrahedron Letters, Vol. 42, Núm. 30, pp. 5017-5019

  2. First efficient preparation of enantiopure 10-bromofenchone: The key intermediate to C10-substituted fenchone-derived chiral sources

    Tetrahedron Letters, Vol. 42, Núm. 37, pp. 6539-6541

  3. Influence of highly preorganised 7,7-diphenylnorbornane in the free energy of edge-to-face aromatic interactions

    Chemistry - A European Journal, Vol. 7, Núm. 6, pp. 1171-1175

  4. Influence of the bridgehead substituent on the stereoselective Leuckart reaction of 2-norbornanones - Skeletal rearrangement versus structural retention

    European Journal of Organic Chemistry, pp. 2805-2808

2000

  1. 7,7-Diarylnorbornanes: Novel Nonclassical NLO-Active Chromophores

    Journal of Physical Chemistry B, Vol. 104, Núm. 1, pp. 43-47