Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes

Synthesis ◽  
2011 ◽  
Vol 2011 (24) ◽  
pp. 4077-4083 ◽  
Author(s):  
Radim Nencka ◽  
Milan Dejmek ◽  
Hubert Hřebabecký ◽  
Michal Šála ◽  
Martin Dračínský
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Solvent Free ◽  
Simple Route ◽  
Microwave Assisted ◽  
Diels Alder Reaction

scholarly journals Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes

Synthesis ◽  
2011 ◽  
Vol 2011 (24) ◽  
pp. e4-e4
Author(s):  
Radim Nencka ◽  
Milan Dejmek ◽  
Hubert Hřebabecký ◽  
Michal Šála ◽  
Martin Dračínský
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Solvent Free ◽  
Simple Route ◽  
Microwave Assisted ◽  
Diels Alder Reaction

Mechanochemical milling promoted solvent-free imino Diels–Alder reaction catalyzed by FeCl3: diastereoselective synthesis of cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines

RSC Advances ◽  
2014 ◽  
Vol 4 (67) ◽  
pp. 35635-35638 ◽  
Author(s):  
Ya-Jun Tan ◽  
Ze Zhang ◽  
Fang-Jian Wang ◽  
Hao-Hao Wu ◽  
Qing-Hai Li
Keyword(s):  
Ball Milling ◽  
Alder Reaction ◽  
Diels Alder ◽  
Solvent Free ◽  
Diastereoselective Synthesis ◽  
Diels Alder Reaction ◽  
Mechanochemical Milling

Cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines were diastereoselectively synthesized by FeCl3-promoted solvent-free Diels–Alder reaction of in situ generated imine with styrene under ball milling.

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