The dimethyl phosphonate hydrophosphonylation of conjugated‐ and non‐conjugated aldehydes into their corresponding α‐hydroxy phosphonates was achieved using chiral aluminum–salalen complex 1 (see scheme).
Synthesis of an Optically Active Al(salalen) Complex and Its Application to Catalytic Hydrophosphonylation of Aldehydes and Aldimines
作者:Bunnai Saito、Hiromichi Egami、Tsutomu Katsuki
DOI:10.1021/ja0651005
日期:2007.2.1
serve as an efficient catalyst for hydrophosphonylation of aldehydes and aldimines, giving the corresponding alpha-hydroxy and alpha-amino phosphonates with high enantioselectivity, respectively. The scope of the hydrophosphonylation was wide, and both aliphatic and aromatic aldehydes and aldimines were successfully used as substrates for the reaction. The potent catalysis of the complex is attributed to
Synthesis and Herbicidal Activities of 2-Methylpropan-2-Aminium Methyl 1-(Substituted Phenoxyacetoxy) Alkylphosphonates
作者:Ling Gao、Xiaoyan Deng、Xiaosong Tan、Qingwu Long、Hao Peng、Hongwu He
DOI:10.1080/10426507.2012.736101
日期:2013.8.1
2-methylpropan-2-aminium methyl1-(substitutedphenoxyacetoxy) alkylphosphonates were selectively synthesized by reacting the corresponding dimethyl 1-(substitutedphenoxyacetoxy)alkylphosphonates with an excess of 2-methylpropan-2-amine. All the title compounds were identified by IR, 1H NMR, and 31P NMR, some of them were further analyzed by 19F NMR and 13C NMR. Their herbicidal activity was investigated and
Mechanistic approach for expeditious and solvent-free synthesis of α-hydroxy phosphonates using potassium phosphate as catalyst
作者:Makarand A. Kulkarni、Uday P. Lad、Uday V. Desai、Satish D. Mitragotri、Prakash P. Wadgaonkar
DOI:10.1016/j.crci.2012.10.009
日期:2013.2
Résumé An extremely simple, high yielding, highly rapid and solvent-free protocol has been described for hydrophosphylation of aldehydes using potassium phosphate as catalyst. Easy commercial availability of the reusable catalyst, operational simplicity at ambient temperature and avoidance of conventional work-up as well as purification procedure makes this solvent-free protocol a near-ideal synthesis. Supplementary Materials: Supplementary material for this article is supplied as a separate file: mmc1.pdf
Kinetic resolution of racemic α-hydroxyphosphonates by asymmetric esterification using achiral carboxylic acids with pivalic anhydride and a chiral acyl-transfer catalyst
作者:Isamu Shiina、Keisuke Ono、Takayoshi Nakahara
DOI:10.1039/c3cc44293d
日期:——
A practical protocol is developed to directly provide chiral alpha-acyloxyphosphonates and alpha-hydroxyphosphonates from (+/-)-alpha-hydroxyphosphonates utilizing the transacylation process to generate the mixed anhydrides from acid components and pivalic anhydride in the presence of organocatalysts (s-value = 33-518).