Biomimetic Reductive Amination of Fluoro Aldehydes and Ketones via [1, 3]-Proton Shift Reaction. 1 Scope and Limitations
T Ono, VP Kukhar, VA Soloshonok
Index: Ono, Taizo; Kukhar, Valery P.; Soloshonok, Vadim A. Journal of Organic Chemistry, 1996 , vol. 61, # 19 p. 6563 - 6569
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Citation Number: 90
Abstract
A systematic study of azomethine-azomethine isomerizations of the N-benzylimines 2, derived from fluorinated aldehydes or ketones and benzylamine, has been made. The results reveal that, in sharp contrast to hydrocarbon analogs, fluorinated imines of 2 in triethylamine solution undergo isomerizations to give the corresponding N-benzylidene derivatives 5 (for 5/2 K> 32) in good isolated yields. The rates of the isomerizations ...
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[Journal of Organic Chemistry, , vol. 61, # 19 p. 6563 - 6569]