93017-30-2

Upstream product

• 923023-81-8 bis(2-phenylethyl)phosphine selenide 
• 108-18-9 diisopropylamine 
• 107-11-9 1-amino-2-propene 
• 100-42-5 styrene 

Downstream Products

• 27440-52-4 bis(2-phenylethyl)phosphine oxide 
• 209742-25-6 5-[2-(Diphenethyl-phosphinoyl)-ethyl]-2-methyl-pyridine 
• 819080-78-9 {2-[(3aR,5R,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yloxy]-ethyl}-diphenethyl-phosphane 
• 854036-30-9 [2-(1H-indol-1-yl)propyl]bis(2-phenylethyl)phosphine 
• 854036-28-5 [2-(2-methyl-4,5,6,7-tetrahydro-1H-indol-1-yl)propyl]bis(2-phenylethyl)phosphine 
• 854036-26-3 [2-(2,3-dimethyl-1H-pyrrol-1-yl)propyl]bis(2-phenylethyl)phosphine 
• 883859-42-5 (Z)-3-[bis(2-phenylethyl)phosphinoyl]-4-hydroxy-4-methyl-2-pentenenitrile 

Relevant academic research and scientific papers

CaII, YbII and SmII Bis(Amido) Complexes Coordinated by NHC Ligands: Efficient Catalysts for Highly Regio- and Chemoselective Consecutive Hydrophosphinations with PH3

The first example of intermolecular hydrophosphination of styrene, 2-vinylpyridine and phenylacetylene with PH3 catalyzed by bis-(amido) complexes [(Me3Si)2N]2M(NHC)2 (M=Ca, Yb, Sm) coordinated by NHC

Radical addition of secondary phosphine chalcogenides to allylamine: Atom-economic synthesis of aminopropylphosphine chalcogenides

Secondary phosphine sulfides and phosphine selenides react with allylamine under the conditions of radical initiation (UV or AIBN) to form the anti-Markovnikov adducts in up to 93 % yield.