Department of Chemistry, Box 298860, Texas Christian University, Fort Worth, Texas 76129, USA.
J Org Chem. 2010 Dec 3;75(23):8166-79. doi: 10.1021/jo101814w. Epub 2010 Nov 2.
Mixed 1,1-bisphosphorus compounds were prepared by the reaction between a phosphonate diester anion and a P(III) chlorophosphine, or its P(V) borane complex. After deprotonation either in situ or in a separate step, the resulting products can be alkylated or reacted with carbonyl compounds. A variety of olefination products were obtained, generally with high E-stereoselectivity. The reaction is competitive with other methods for the synthesis of alkenyl phosphorus compounds, and in the case of trisubstituted alkenes, regio- and stereocontrolled olefination provides products not easily accessible via any other process. The deprotection of phosphine-borane adducts was also demonstrated. Overall, a variety of novel organophosphorus reagents and products were synthesized easily and in good yields.
混合 1,1-双膦化合物是通过膦酸二酯阴离子和 P(III)氯代膦,或其 P(V)硼烷配合物之间的反应制备的。在原位或在单独的步骤中脱质子化后,所得产物可以被烷基化或与羰基化合物反应。得到了各种烯烃化产物,通常具有高的 E-立体选择性。该反应与其他合成烯基磷化合物的方法具有竞争性,并且在三取代烯烃的情况下,区域和立体选择性的烯烃化提供了通过任何其他方法不易获得的产物。膦-硼烷加合物的脱保护也得到了证明。总的来说,各种新型有机磷试剂和产物都可以很容易地以良好的收率合成。