Montmorillonita Catalizador ecológico y eficaz en la síntesis de compuestos biológicamente activos con Bicyclo
Video Experimental Relacionado
Updated: Jan 7, 2026

10:17
Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
7.3K
Eva Vrbková1, Lucie Stoupová1, Eliška Vyskočilová1
1Department of Organic Technology, University of Chemistry and Technology Prague, Technická 6, 166 28 Prague, Czech Republic.
ACS omega
|January 5, 2026
Resumen
No abstract available in PubMed .
Más Videos Relacionados
Videos de Conceptos Relacionados
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.5K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.5K
Cycloaddition Reactions: MO Requirements for Thermal Activation
4.1K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
4.1K
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
2.2K
The radical dimerization of ketones or aldehydes gives vicinal diols through a pinacol coupling reaction. However, the behavior of titanium metals used for the reaction as a source of electrons is unusual. When the reaction is carried out in the presence of titanium, diols can be isolated at low temperatures. Else titanium further reacts with diols, forming alkenes through the McMurry reaction.
2.2K

