论文信息 - Solvent free reaction under microwave irradiation: A new procedure for Eu+3 — Catalyzed Michael addition of 1,3-dicarbonyl compounds - 字舞流文

Solvent free reaction under microwave irradiation: A new procedure for Eu+3 — Catalyzed Michael addition of 1,3-dicarbonyl compounds

CC bond formation via Michael addition is achieved in high yields and short times by employing catalytic amounts of EuCl3 in dry media under microwave irradiation.

Manuela Giordano | M. Giordano | M. D. Rosa | A. Soriente | A. Scettri | Arrigo Scettri | Aldo Spinella | Annunziata Soriente | Margherita De Rosa | A. Spinella

[1] Raymond J. Giguere,et al. Application of commercial microwave ovens to organic synthesis. , 1986 .

[2] C. R. Strauss,et al. Development and Application of a Continuous Microwave Reactor for Organic Synthesis , 1994 .

[3] R. Gedye,et al. The use of microwave ovens for rapid organic synthesis , 1986 .

[4] Ken-ichi Watanabe,et al. Michael Additions Catalyzed by Metal(II) Complexes , 1982 .

[5] André Lubineau,et al. Water-promoted organic reactions. Michael addition of nitroalkanes to methylvinylketone under neutral conditions , 1992 .

[6] P. Laszlo,et al. Dual catalysis of the michael reaction , 1990 .

[7] A. Scettri,et al. Lanthanides in organic synthesis: Eu+3-catalyzed Michael addition of 1,3- dicarbonyl compounds , 1993 .

[8] D. Michael P. Mingos,et al. Applications of Microwave Dielectric Heating Effects to Synthetic Problems in Chemistry , 1991 .