MA Fernández-Herrera, H López-Muñoz… - Bioorganic & Medicinal …, 2010 - Elsevier
Certain steroidal compounds have demonstrated an antiproliferative effect against several tumor cell lines; however, their complete role on cancer cells is not currently established …
A Romero-López, S Montiel-Smith, S Meza-Reyes… - Steroids, 2014 - Elsevier
An efficient and facile synthesis of fused, substituted and spiro pyrazoline steroid derivatives through a cycloaddition reaction of different α, β-unsaturated ketones with hydrazine acetate …
A new transformation of the spiroketal side chain of diosgenin is reported: treatment of 23- hydroxyiminodiosgenin acetate with phosphorous oxychloride in pyridine produced an …
The new (22R, 23S, 25R)-3β, 16β, 26-triacetoxy-cholest-5-ene-22, 23-diol () was synthesized from diosgenin () through a synthetic route based on chemoselective RuO4 …
The side–chain opening of 25R and 25S steroidal sapogenins to form 22–oxocholestanic skeletons is described. The transformation was produced under mild conditions providing …
MA Iglesias-Arteaga, GA Velázquez-Huerta - Tetrahedron letters, 2005 - Elsevier
Favorskii rearrangement of 23-oxo-3-epi-smilagenin acetate induced by iodosobenzene - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …
One-step axial acetoxylation at C-23. A new method for the functionalization of the side chain of steroid sapogenins - ScienceDirect Skip to main contentSkip to article Elsevier logo …
Pyrazoline steroids are electron-rich nitrogen-containing heterocyclic structures that exhibit several desirable pharmacological features. Conventional synthetic techniques to obtain …
Abstract The Baeyer-Villiger reactions of 25R-and 25S-23-oxosapogenins with MCPBA produced a mixture of bisnorcholanic 22→ 16 lactones and pregnan-16, 20-diol carbonates …