scholarly journals Asymmetric Diels–Alder Reactions of an Acrylic Acid Derivative Using a Chiral Titanium Catalyst

1991 ◽  
Vol 64 (2) ◽  
pp. 387-391 ◽  
Author(s):  
Koichi Narasaka ◽  
Hiroko Tanaka ◽  
Fumihiko Kanai
ACS Catalysis ◽  
2015 ◽  
Vol 5 (11) ◽  
pp. 6946-6955 ◽  
Author(s):  
Eyas Mahmoud ◽  
Jingye Yu ◽  
Raymond J. Gorte ◽  
Raul F. Lobo

1977 ◽  
Vol 55 (21) ◽  
pp. 3763-3773 ◽  
Author(s):  
P. de Mayo ◽  
H. Y. Ng

The irradiation of 4,5-benzo-1,2-dithiole-3-thione (1) in the presence of cyclopentene and of tetramethylethylene gives 1:1 adducts. In solution these adducts are in equilibrium with eight-membered-ring dimers. The thermodynamic parameters for this equilibrium have been determined. The available evidence suggests a head-to-head configuration. These same monomeric adducts give Diels–Alder addition products with normal dienophiles, but also react similarly with simple thiones (adamantanethione, norbornanethione, cyclohexanethione) to give thioorthoesters. The structures of the latter substances have been demonstrated both spectroscopically and, chemically, by hydrolysis to a thiosalicylic acid derivative. The thioorthoesters have been shown to undergo stereoisomerization on acid catalysis. Of the two mechanisms considered for this process (reversal to thiones and ion-pair formation) the former has been excluded.


2001 ◽  
Vol 170 (1) ◽  
pp. 187-190 ◽  
Author(s):  
Majid M. Heravi ◽  
Naser Montazeri ◽  
Mohammad Rahimizadeh ◽  
Mehdi Bakavoli ◽  
Mitra Ghassemzadeh
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