Gema Cabrero

Organocatalytic Ring Expansion of β-Lactams to γ-Lactams through a Novel N1−C4 Bond Cleavage. Direct Synthesis of Enantiopure Succinimide Derivatives

Benito Alcaide, Pedro Almendros, Gema Cabrero et al. · Organic Letters · 2005 · 73 citations

Pharmacy, Chemistry, Medicinal Chemistry +13

Direct organocatalytic synthesis of enantiopure succinimides from β-lactam aldehydes through ring expansion promoted by azolium salt precatalysts

Benito Alcaide, Pedro Almendros, Gema Cabrero et al. · Chemical Communications · 2007 · 49 citations

Natural Sciences, Chemistry, Catalysis +8

Ring Expansion <i>versus</i> Cyclization in 4‐Oxoazetidine‐2‐ carbaldehydes Catalyzed by Molecular Iodine: Experimental and Theoretical Study in Concert

Benito Alcaide, Pedro Almendros, Gema Cabrero et al. · Advanced Synthesis & Catalysis · 2010 · 37 citations

Natural Sciences, Chemistry, Medicinal Chemistry +14

Stereocontrolled Access to Orthogonally Protected <i>anti</i>,<i>anti</i>-4-Aminopiperidine-3,5-diols through Chemoselective Reduction of Enantiopure β-Lactam Cyanohydrins

Benito Alcaide, Pedro Almendros, Gema Cabrero et al. · The Journal of Organic Chemistry · 2007 · 28 citations

Natural Sciences, Chemistry, Medicinal Chemistry +13

Stereoselective cyanation of 4-formyl and 4-imino-?-lactams: application to the synthesis of polyfunctionalized ?-lactams

Benito Alcaide, Pedro Almendros, Gema Cabrero et al. · Tetrahedron · 2012 · 19 citations · Full text

Natural Sciences, Chemistry, Medicinal Chemistry +10