431875-41-1

Upstream product

• 921-26-6 N,N-diisopropylphosphoramide dichloride 
• 2548-47-2 2,3-diphenyl-1,3-butadiene 

Downstream Products

• 431875-39-7 cis-dichloro-bis-(1-diisopropylamino-3,4-diphenylphosphole)platinum(II) 
• 432038-72-7 trans-dichloro-bis-(1-diisopropylamino-3,4-diphenylphosphole)platinum(II) 
• 431875-35-3 bis-[μ-chloro-chloro-(1-diisopropylamino-3,4-diphenylphosphole)palladium(II)] 
• 433267-13-1 2,5-dibromo-2,5-dihydro-1-(diisopropylamino)-3,4-diphenylphosphole 1-sulfide 
• 433267-12-0 2,5-dibromo-2,5-dihydro-1-(diisopropylamino)-3,4-diphenylphosphole 1-oxide 
• 433267-16-4 2-bromo-1-(diisopropylamino)-3,4-diphenylphosphole 1-sulfide 
• 433267-10-8 1-(diisopropylamino)-3,4-diphenylphosphole 1-oxide 

Relevant academic research and scientific papers

A convenient procedure for the preparation of 1-(diisopropylamino)phospholes - Application to the synthesis of new 2,2′-biphosphole disulfides

A convenient one-pot procedure for the preparation of 1-(diisopropylamino)phospholes has been developed. These phospholes have been used in a multistep procedure for synthesizing two new 2,2′-biphosphole disulfide compounds. The structures and stereochemistry of these compounds have been studied by X-ray diffraction analysis and by molecular modeling. The 1-(diisopropylamino) group, used as a bulky substituent on the phosphorus atom in combination with a phenyl group on the ring, proved to be an important factor in the stabilization of the axial chirality of 2,2′-biphosphole framework.