Chemical consequences of fluorine substitution. Part 4. Diels–Alder reactions of fluorinated p-benzoquinones with Dane's diene. Synthesis of fluorinated D-homosteroids

Author(s):  
Michael Essers ◽  
Günter Haufe
2001 ◽  
Vol 79 (12) ◽  
pp. 1906-1909 ◽  
Author(s):  
Christopher K Jankowski ◽  
Gaëtan LeClair ◽  
Jacqueline MR Bélanger ◽  
Jocelyn RJ Paré ◽  
Marie-Rose VanCalsteren

The synthesis of isoquinolinone carboxylates was performed using arecoline or its isomer N-methyl tetrahydro pyridine carboxylate with Danishefsky's diene via thermal or microwave assisted Diels-Alder reaction. The comparison of both condensation modes showed that the microwave method not only afforded higher yields of the adducts, but also lead to the formation of a new α,β-unsaturated pyridyl ketone. All structures were identified with the help of high resolution 2D NMR.Key words: Diels-Alder microwave assisted reaction, microwave synthesis, Michael, diene, isoquinoline carboxylate synthesis, Danishefsky diene synthesis, MAP Diels-Alder2.


Tetrahedron ◽  
1996 ◽  
Vol 52 (18) ◽  
pp. 6325-6338 ◽  
Author(s):  
Teh-Chang Chou ◽  
Pao-Chiung Hong ◽  
Yane-Fong Wu ◽  
Wen-Yean Chang ◽  
Cheng-Tung Lin ◽  
...  

1942 ◽  
Vol 31 (2) ◽  
pp. 319-523 ◽  
Author(s):  
James A. Norton
Keyword(s):  

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