Diethyl oxaloacetate. Nonconcerted general catalysis of enolization, tertiary amine catalyzed enolization via an addition-elimination mechanism, and general-acid-catalyzed dehydration and cleavage

1978 ◽  
Vol 100 (15) ◽  
pp. 4802-4808 ◽  
Author(s):  
Paula Yurkanis Bruice ◽  
Thomas C. Bruice

1983 ◽  
Vol 48 (23) ◽  
pp. 4175-4179 ◽  
Author(s):  
James L. Jensen ◽  
Anna B. Martinez ◽  
Cheryl L. Shimazu


1970 ◽  
Vol 48 (2) ◽  
pp. 263-270 ◽  
Author(s):  
J. M. McAndless ◽  
Ross Stewart

Proton magnetic resonance spectroscopy has been used to examine the deuterium exchange of the methyl protons in two lumazine derivatives. The exchange occurs at the C-7 methyl group in 6,7,8-trimethyllumazine (2) and at the C-6 methyl group in 1,7-dihydro-6,7,8-trimethyllumazine (3). The former reaction is subject to both general acid- and general base-catalysis but the latter only to general acid-catalysis. Plausible mechanisms for the reactions of both compounds are advanced, involving in the case of 3, acid-catalyzed addition of water across the C6—N5 double bond.



1979 ◽  
Vol 8 (3) ◽  
pp. 229-232 ◽  
Author(s):  
Seiji Shinkai ◽  
Tetsuya Nakano ◽  
Hisatake Hamada ◽  
Yumiko Kusano ◽  
Osamu Manabe




1954 ◽  
Vol 76 (17) ◽  
pp. 4379-4381 ◽  
Author(s):  
Robert H. DeWolfe ◽  
Royston M. Roberts




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