78731-75-6Relevant academic research and scientific papers
Catalytic Hydrophosphination of Alkenylalkyl Ethers
Kazankova, Marina A.,Shulyupin, Mstislav O.,Beletskaya, Irina P.
, p. 2155 - 2158 (2003)
Hydrophosphination of alkenylalkyl ethers catalyzed by Pd- and Ni-complexes is described. The reaction is regioselective giving only Markovnikov product isolated as α-alkoxyalkyldiphenyl oxide after oxidation by H2O2.
Hydrophosphination of alkoxyalkenes catalyzed by transition metal complexes
Shulyupin,Trostyanskaya,Kazankova,Beletskaya
, p. 17 - 22 (2007/10/03)
Diphenylphosphine adds to alkyl vinyl ethers in the presence of Ni(II) and Pd(II) complexes with a high regioselectivity, leading to exclusive formation of the corresponding Markownikoff adducts which were isolated as 1-alkoxyalkyl(diphenyl)phosphine oxid
ZUR REAKTION PRIMAERER AND SEKUNDAERER PHOSPHINE MIT AROMATISCHEN ALDEHYDEN UND ALKOHOLEN
Oehme, H.,Leissring, E.
, p. 753 - 759 (2007/10/02)
PH-Phosphines react with aromatic aldehydes in an alcohol under P-C-O-bond formation to give α-alcoxy benzylphosphines R2P-CH(Ph)-OR' or R-2 resp.In case of 4-dimethylaminobenzaldehyde or 2,4-dimethoxybenzaldehyde with diphenylphosphine or phe
