53378-80-6Relevant articles and documents
Reactions of α-phosphoryl-α-haloacetaldehydes with difunctional nucleophiles
Asadov,Burangulova,Guseinov
, p. 508 - 511 (2005)
Reactions of phosphorylated α-haloacetaldehydes with difunctional nitrogen-, oxygen-, and sulfur-containing nucleophiles were performed with a view to synthesize C-phosphorylated heterocyclic compounds.
Mild synthesis of organophosphorus compounds: Reaction of phosphorus-containing carbenoids with organoboranes
Antczak, Monika I.,Montchamp, Jean-Luc
supporting information; experimental part, p. 977 - 980 (2009/04/10)
Organoboranes react with phosphorus-containing carbenoids to produce a variety of functionalized organophosphorus compounds under mild conditions. In some cases, selective migration of one group atached to boron can be observed. Phosphonite-borane complexes are introduced as novel synthons for the synthesis of phosphinic esters.
Synthesis, reactivity and stereochemistry of new phosphorus heterocycles with 5- or 6-membered rings
Cristau, Henri-Jean,Pirat, Jean-Luc,Virieux, David,Monbrun, Jér?me,Ciptadi, Ciptadi,Bekro, Yves-Alain
, p. 2472 - 2481 (2007/10/03)
Syntheses of novel phosphorus heterocycles containing α-amino or α-hydroxyphosphonic or phosphinic acids motifs are developed. 2,3-dihydro-1,3-oxaphospholes (1) and 1,4,2-oxazaphosphinanes (2) exhibit a reactive part, respectively the enolether moiety and the P-H bond, which allows various structural modifications: (i) for 1a, by introduction of amino substituents, (ii) for 2a, by hydroxy- or aminoalkylation, by Michael addition or by P-arylation. These reactions present generally a good or even an excellent kinetic diastereoselectivity which can often be predicted by molecular models of the transition states.