HClO4-SiO2 as a Novel and Recyclable Catalyst for the Phospha-Michael Addition of Phosphorous Nucleophiles to α,β-Unsaturated Malonates
作者:Sara Sobhani、Soodabeh Rezazadeh
DOI:10.1055/s-0029-1220069
日期:2010.6
An efficient synthesis of β-phosphono malonates via phospha-Michael addition of phosphorous nucleophiles to α,β-unsaturated malonates in the presence of HClO4-SiO2 as a new and recyclable catalyst is described.
Phospha-Michael addition of diethyl phosphite to α,β-unsaturated malonates catalyzed by nano γ-Fe2O3-pyridine based catalyst as a new magnetically recyclable heterogeneous organic base
Nano γ-Fe2O3-pyridine based catalyst as a new magnetically recyclable heterogeneous organic base was synthesized. The synthesized odorless pyridine based catalyst was used as a new catalyst for the efficient synthesis of β-phosphonomalonates by the reaction of diethyl phosphite with α,β-unsaturated malonates. The catalyst was easily isolated from the reaction mixture by a magnetic bar and reused at
Phospha-Michael addition of phosphorus nucleophiles to α,β-unsaturated malonates using 3-aminopropylated silica gel as an efficient and recyclable catalyst
gel, which is prepared from commercially available and cheap starting materials, is introduced as an efficient and recyclable catalyst for the phospha-Michael addition of phosphorus nucleophiles to α,β-unsaturated malonates. Short reaction times, mild reaction conditions, ease of recovery and catalyst reusability make this method a new, economic and waste-free chemical process for the synthesis of β-phosphonomalonates
Zeolitic imidazolate frameworks as heterogeneous catalysts for a one-pot P–C bond formation reaction via Knoevenagel condensation and phospha-Michael addition
ZIF-8 promotes a sequential one-pot reaction efficiently to produce organophosphorus compounds via Knoevenagel condensation and phospha-Michael addition.