Publicacions en col·laboració amb investigadors/es de Instituto de Productos Naturales y Agrobiología (13)

2005

  1. A modular, one-pot, four-component synthesis of polysubstituted 1,3-oxazolidines

    Journal of Organic Chemistry, Vol. 70, Núm. 3, pp. 1042-1045

  2. Multicomponent domino processes based on the organocatalytic generation of conjugated acetylides: Efficient synthetic manifolds for diversity-oriented molecular construction

    Chemistry - A European Journal, Vol. 11, Núm. 12, pp. 3503-3510

2004

  1. A diversity-oriented strategy for the construction of tetrasubstituted pyrroles via coupled domino processes

    Journal of the American Chemical Society, Vol. 126, Núm. 27, pp. 8390-8391

2003

  1. An effective one-pot synthesis of 5-substituted tetronic acids

    Journal of Organic Chemistry, Vol. 68, Núm. 8, pp. 3363-3365

  2. Efficient domino process based on the catalytic generation of non-metalated, conjugated acetylides in the presence of aldehydes or activated ketones

    Chemistry - A European Journal, Vol. 9, Núm. 13, pp. 3122-3131

2001

  1. Alkynoates as a source of reactive alkylinides for aldehyde addition reactions

    Organic Letters, Vol. 3, Núm. 12, pp. 1905-1907

  2. Enantioselective synthesis of medium-sized ring-bridged oxabicycles by ring-closing metathesis

    European Journal of Organic Chemistry, pp. 4423-4429

1998

  1. Diastereoselective formal synthesis of the antifungal agent, (+)- Preussin. A new entry to chiral pyrrolidines

    Tetrahedron Letters, Vol. 39, Núm. 1-2, pp. 131-134

  2. Tetralkylammonium permanganate epoxidation of an unreactive double bond by an intramolecular oxygen-atom transfer process

    Chemistry Letters, pp. 25-26

1997

  1. Design and synthesis of a new tricyclic scaffold for molecular recognition

    Tetrahedron Letters, Vol. 38, Núm. 45, pp. 7911-7912

  2. Sodium borohydride-amberlyst-15 (H+): An effective reductor for hindered and unreactive ketones in aprotic solvent

    Tetrahedron Letters, Vol. 38, Núm. 2, pp. 277-280

  3. Stereoselective radical C-C bond forming using Suarez' protocol: A non reductive process

    Tetrahedron Letters, Vol. 38, Núm. 46, pp. 8081-8084

1992

  1. Lewis acid-mediated isomerisation of (25R)-3β-acetoxy-5α- spirostan-23-one, a C-22 spiroacetal: An approach to the synthesis of C-23 spiroacetal steroidal sapogenins

    Journal of the Chemical Society, Chemical Communications, pp. 275-277