119623-47-1Relevant academic research and scientific papers
Iron-catalyzed cross coupling of P-H/C-O bonds: Efficient synthesis of α-alkoxyphosphorus compounds
Li, Xue,Chen, Tieqiao,Saga, Yuta,Han, Li-Biao
supporting information, p. 1877 - 1880 (2016/02/05)
An efficient P-C bond-formation through iron-catalyzed cross coupling of P-H/C-O bonds is developed for the first time. This reaction proceeds efficiently to produce the corresponding valuable α-alkoxyphosphorus compounds under mild conditions with a wide generality.
2-Methoxy-1,3-dienes - Preparation via α-Methoxyallylphosphine Oxides using a One-pot Wittig-Horner Reaction
Birse, Ewan F.,Maleki, Mehran,Miller, J. Allen,Murray, Alistair W.
, p. 864 - 872 (2007/10/02)
2-Methoxy-1,3-dienes bearing an aryl group at position 1 and/or 4 are readily available in a one-pot Wittig-Horner reaction using α-methoxyallylphosphine oxides (1a) or (1b).
REGIOCHEMISTRY OF REACTIONS OF α-ALKOXYALLYLPHOSPHINE OXIDE YLIDES WITH ELECTROPHILES.
Maleki, Mehran,Miller, J. Allen,Lever, O. William
, p. 3789 - 3792 (2007/10/02)
Anions 4, derived from α-methoxyallylphosphine oxides 3, react with electrophiles in a highly regioselective fashion to give products of α-attack or γ-attack depending upon the substitution pattern of the ylid 4 and the nature of the electrophile.
