Publicaciones en las que colabora con HUMBERTO RODRIGUEZ SOLLA (11)

2013

  1. Stereoselective synthesis of carbohydrate-derived N-Sulfonyl aziridines

    Synlett, Vol. 24, Núm. 2, pp. 181-184

  2. Synthesis of highly functionalized enantiopure halocyclopropanes derived from carbohydrates

    European Journal of Organic Chemistry, pp. 4953-4961

2012

  1. Asymmetric construction of quaternary stereocenters: Synthesis of enantiopure amino acid-based tricyclic α,β-enones through an ipso-Friedel-Crafts/Michael addition cascade

    Advanced Synthesis and Catalysis, Vol. 354, Núm. 2-3, pp. 295-300

  2. Samarium-promoted asymmetric aldol-Tishchenko reaction: Synthesis of amino acid-derived 4-amino-1,3-diols

    Advanced Synthesis and Catalysis, Vol. 354, Núm. 9, pp. 1679-1684

2011

  1. An efficient catalytic chromium-mediated iodocyclopropanation Reaction: Stereoselective synthesis of iodocyclopropanecarboxamides

    Advanced Synthesis and Catalysis, Vol. 353, Núm. 1, pp. 49-52

2009

  1. Highly stereoselective halocyclopropanation of α,β-unsaturated amides

    Advanced Synthesis and Catalysis, Vol. 351, Núm. 13, pp. 2185-2198

  2. The addition reaction of samarium enolates and 2-haloenolates derived from esters, and amides to imines. totally stereoselective synthesis of enantiopure 3,4-diamino esters or amides

    Advanced Synthesis and Catalysis, Vol. 351, Núm. 17, pp. 2991-3000

2008

  1. CrCl2-promoted stereospecific and stereoselective alkyl- and silylcyclopropanation of α,β-unsaturated amides

    Journal of Organic Chemistry, Vol. 73, Núm. 10, pp. 3828-3836

  2. Stereospecific and stereoselective alkyl and silylcyclopropanation of α,β-unsaturated amides

    Organic Letters, Vol. 10, Núm. 2, pp. 349-352

  3. Totally selective synthesis of enantiopure (3S,5S)- and (3R,5R)-4-amino-3, 5-dihydroxypiperidines from aminodiepoxides derived from serine

    Journal of Organic Chemistry, Vol. 73, Núm. 15, pp. 6048-6051

2006

  1. Efficient addition reaction of bromonitromethane to aldehydes catalyzed by Nal: A new route to 1-bromo-1-nitroalkan-2-ols under very mild conditions

    Organic Letters, Vol. 8, Núm. 26, pp. 5979-5982