Publications in collaboration with researchers from Universidad Autónoma de Madrid (19)

2020

  1. BODIPYs revealing lipid droplets as valuable targets for photodynamic theragnosis

    Chemical Communications, Vol. 56, Núm. 6, pp. 940-943

  2. Exploring BODIPY Derivatives as Singlet Oxygen Photosensitizers for PDT

    Photochemistry and Photobiology, Vol. 96, Núm. 3, pp. 458-477

2017

  1. A versatile fluorescent molecular probe endowed with singlet oxygen generation under white-light photosensitization

    Dyes and Pigments, Vol. 142, pp. 77-87

  2. Rational Design of Advanced Photosensitizers Based on Orthogonal BODIPY Dimers to Finely Modulate Singlet Oxygen Generation

    Chemistry - A European Journal, Vol. 23, Núm. 20, pp. 4837-4848

2014

  1. Circularly polarized luminescence by visible-light absorption in a chiral o-bodipy dye: Unprecedented design of cpl organic molecules from achiral chromophores

    Journal of the American Chemical Society, Vol. 136, Núm. 9, pp. 3346-3349

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

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

2005

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

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

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

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

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

2000

  1. Erratum: A new highly efficient synthetic route to enantiopure 10-bromocamphor (Tetrahedron: Asymmetry 11 (2000) (3059) PII: S0957416600002792)

    Tetrahedron Asymmetry

1997

  1. Synthesis of methyl (1R,2S)-α,α-dimethyl-3-oxo-2-pentylcyclopentaneacetate. A model procedure for the preparation of chiral jasmonoids and prostaglandins

    Tetrahedron Asymmetry, Vol. 8, Núm. 6, pp. 849-852

1996

  1. A facile synthesis of new homochiral β-amino alcohols with norbornane framework

    Tetrahedron Asymmetry, Vol. 7, Núm. 5, pp. 1257-1260