79032-37-4

Upstream product

• 501-65-5 diphenyl acetylene 
• 30540-36-4 3,4-dimethyl-1-phenylphosphole 
• 79032-35-2 3,4-Dimethyl-5-phenyl-2H-phosphole 

Downstream Products

• 79032-35-2 3,4-Dimethyl-5-phenyl-2H-phosphole 
• 79032-36-3 4,5-dimethyl-2,3,6-triphenyl-1-phosphanorborna-2,5-diene 1-sulfide 
• 1254944-69-8 C₂₆H₂₃O₂P 

Relevant academic research and scientific papers

Hetero-Diels-Alder reactions of 2H-phospholes with aldehydes

Transient 2-phenyl-3,4-dimethyl-5H-phosphole reacts at 150 °C with aldehydes RCH=O to give the corresponding [4 + 2] P-O cycloadducts with endo- b(major) and exo-R-substituents. The cycloaddition with α,β-unsaturated aldehydes takes place both at the C=O

A new versatile route for the conversion of phospholes into phosphinines

(Figure Presented) En route to phosphinines: An efficient route to convert 1-phosphanorbornadienes into phosphinines is described (see scheme). This opens up the possibiltiy to use the broad and versatile phosphole chemistry as a starting point for an equ

3,4-dimethyl-2,5,6-tris(p-sulfonatophenyl)-1-phosphanorbornadiene, process for the preparation thereof and process for the hydroformylation of olefinnically unsaturated compounds

The chemical compound 3,4-dimethyl-2,5,6-tris(p-sulfonatophenyl)-1-phosphanorbernadiene, a process for the preparation thereof and a process for the hydroformylation of olefinically unsaturated compounds with the use of catalysts which contain the aforeme