ChemInform Abstract: SUBSTITUENT EFFECTS IN THE DIELS-ALDER REACTION OF SUBSTITUTED BENZYNES WITH HEXAMETHYLCYCLOHEXA-2,4-DIENONE

1978 ◽  
Vol 9 (8) ◽  
Author(s):  
A. OKU ◽  
A. MATSUI
Tetrahedron ◽  
1994 ◽  
Vol 50 (23) ◽  
pp. 6767-6782 ◽  
Author(s):  
Brian J. McNelis ◽  
Daniel D. Sternbach ◽  
Andrew T. MacPhail

2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Mujeeb A. Sultan ◽  
Usama Karama

Diels-Alder reaction of 10-allyl-1,8-dichloroanthracene (3) with 2-chloroacrylonitrile (4) and 1-cyanovinyl acetate (5) gives exclusively theorthoisomer while its reaction with phenyl vinyl sulfone (10) yields a mixture of two isomeric adducts with priority toorthoisomer. The reactions proceeded under microwave condition in xylene. Configurations of these isomers have been assigned with the help of NMR spectra. The results indicated that the steric effect is dominating toward the isomer regioselectivity in the Diels-Alder reaction of the present compounds.


1996 ◽  
Vol 61 (15) ◽  
pp. 5121-5129 ◽  
Author(s):  
Vincenzo Barone ◽  
Roger Arnaud ◽  
Pierre Yves Chavant ◽  
Yannick Vallée

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