3167-63-3Relevant articles and documents
A Convenient Synthesis of Diethyl 1-Chloroalkylphosphonates
Gajda, Tadeusz
, p. 717 - 718 (1990)
The title compounds were obtained in high yield by the reaction of diethyl 1-hydroxyalkylphosphonates with triphenylphosphine carbon tetrachloride.
SYNTHESIS OF INTERMEDIATES USED IN THE MANUFACTURE OF ANTI-HIV AGENTS
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Page/Page column 25-26, (2016/11/21)
The present invention relates to a process of preparing intermediates of Formula (I). The process comprises of reacting compound of Formula (III) with compound of Formula (V) in the presence of a solvent selected from an alcohol, ether or water to form compound of Formula (I) wherein, R1 is selected from –NH2, Cl, Br, NHCOR", wherein R" is alkyl, aryl, Schiff's base of formula N=CHR', wherein R' is alkyl or aryl; R2 is selected from H, alkyl; R3 and R4, each independently is H; R5 and R6, each independently is H, alkyl; R7 is H, alkyl; and R8 is H, alkyl.
Reactions of α-boranophosphorus compounds with electrophiles: Alkylation, acylation, and other reactions
Antczak, Monika I.,Montchamp, Jean-Luc
supporting information; experimental part, p. 3758 - 3766 (2009/11/30)
(Chemical Equation Presented) The homologation of phosphorus carbenoids with organoboranes leads to α-boranophosphorus compounds, which can be further functionalized through reactions with various electrophiles, either directly or after activation to the