Steric Effects in Elimination Reactions. VIII. The Effect of the Steric Requirements of Pyridine Bases on the Direction of the Elimination Reaction

1956 ◽  
Vol 78 (10) ◽  
pp. 2197-2199 ◽  
Author(s):  
Herbert C. Brown ◽  
M. Nakagawa
2019 ◽  
Vol 123 (41) ◽  
pp. 8776-8786
Author(s):  
Timothy M. Brown ◽  
Blanton R. Gillespie ◽  
Mallory M. Rothrock ◽  
Anthony J. Ranieri ◽  
Melinda K. Schueneman ◽  
...  

1975 ◽  
Vol 97 (15) ◽  
pp. 4323-4327 ◽  
Author(s):  
James L. Coke ◽  
G. Dale Smith ◽  
George H. Britton

1972 ◽  
Vol 50 (8) ◽  
pp. 1188-1191
Author(s):  
George H. Schmid ◽  
Aaron W. Wolkoff

A comparison of the products from elimination reactions of a number of compounds containing various leaving groups with those containing the N-methyl oxypyridinium leaving group suggests that the elimination is not occurring by means of a simple E1 mechanism. Changing the anion of the salt from iodide to methyl-sulphate and tetrafluoroborate affects the product composition indicating that the anion is taking part in the reaction. The mechanism of this reaction appears to be on the E1-E2 borderline.


2015 ◽  
Vol 119 (17) ◽  
pp. 3887-3896 ◽  
Author(s):  
Leah N. Wormack ◽  
Meghan E. McGreal ◽  
Corey E. McClintock ◽  
George L. Heard ◽  
D. W. Setser ◽  
...  

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