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Reactivity of Mannich bases. Part XIII. Mechanism of the reaction between aminomethylnaphthols and benzenethiols

✍ Scribed by Andrisano, R.; Casa, C. Della; Tramontini, M.

Book ID
120337935
Publisher
The Royal Society of Chemistry
Year
1970
Tongue
English
Weight
451 KB
Volume
13
Category
Article
ISSN
0022-4952

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## Abstract The electron structures of various unstable N‐methylolamines and their imine cations formed during the urotropine nitrolysis process were studied by SCF‐CNDO/2 computation. The relative tendency of forming imine cations from such N‐methylolamine molecules was assessed by the computation