Jana Špaková Raschmanová

Creation of quarternary stereocentres via [3,3]-sigmatropic rearrangement of allylic thiocyanates. A synthetic approach to (+)-myriocin

Jozef Gonda, Miroslava Martinková, Jana Špaková Raschmanová et al. · Tetrahedron Asymmetry · 2006 · 38 citations

Enantioselective Synthesis, Bioorganic Chemistry, Engineering +10

Microwave accelerated aza-Claisen rearrangements

Jozef Gonda, Miroslava Martinková, Andrea Zadrošová et al. · Tetrahedron Letters · 2007 · 33 citations

Cross-coupling Reaction, Engineering, Aza-claisen Rearrangements +5

Total synthesis of a protected form of sphingofungin E using the [3,3]-sigmatropic rearrangement of an allylic thiocyanate as the key reaction

Miroslava Martinková, Jozef Gonda, Jana Špaková Raschmanová et al. · Carbohydrate Research · 2010 · 26 citations

Bioorganic Chemistry, Biochemistry, Natural Sciences +9

Novel Furanoid α-Substitued α-Amino Acid as a Potent Turn Mimic in Peptide Synthesis

Miroslava Martinková, Jozef Gonda, Jana Špaková Raschmanová · Molecules · 2006 · 23 citations · Full text

Stereoselective synthesis of both enantiomers of α-(hydroxymethyl)glutamic acid

Miroslava Martinková, Jozef Gonda, Jana Špaková Raschmanová et al. · Tetrahedron Asymmetry · 2008 · 15 citations

Diversity-oriented Synthesis, Organic Chemistry, Stereoselective Synthesis +3