Universidad Autónoma de Madrid-ko ikertzaileekin lankidetzan egindako argitalpenak (20)

2024

  1. A highly fluorescent and readily accessible all-organic photosensitizer model for advancing image-guided cancer PDT

    Journal of Materials Chemistry B, Vol. 12, Núm. 31, pp. 7618-7625

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