1,3,5-Triaza-7-phosphaadamantane,min.97%

Reaction

1. Air-stable, water-soluble version of trimethylphosphine.
2. Reagent used in the β-olefination of 2-alkynoates leading to trisubstituted 1,3-dienes.
3. Ligand/rhodium catalyst used in the branch selective allylation of acetylacetone.
4. Ligand/oxorhenium complex used as a catalyst for the Baeyer-Villiger oxidation of ketones. 

Uses

• The molecular mechanisms of antimetastatic ruthenium compounds explored through DIGE proteomics.: This study examines the antimetastatic properties of ruthenium compounds using DIGE proteomics. The involvement of 1,3,5-Triaza-7-phosphaadamantane in the complexation with ruthenium and its biological effects were analyzed, highlighting its potential in anticancer therapies (Guidi et al., 2013).
• Synthesis, antimicrobial and antiproliferative activity of novel silver(I) tris(pyrazolyl)methanesulfonate and 1,3,5-triaza-7-phosphadamantane complexes.: This research details the synthesis of novel silver complexes containing 1,3,5-Triaza-7-phosphaadamantane, evaluating their antimicrobial and antiproliferative activities, which demonstrates the compound′s utility in biomedical applications (Pettinari et al., 2011).

General Description

Air stable organocatalyst for Baylis-Hillman transformation

reaction suitability

reagent type: ligand
reaction type: Hydroformylations
reagent type: ligand
reaction type: Hydrogenations
reagent type: ligand
reaction type: Morita-Baylis-Hillman Reactions
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling