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Electronic structure and reactivity of mono-N-arylamides of maleic acid in the reaction with decanethiol

✍ Scribed by V. M. Gun'ko; Yu. V. Tanchuk; L. M. Roev

Book ID
112363318
Publisher
Springer
Year
1982
Tongue
English
Weight
439 KB
Volume
18
Category
Article
ISSN
0040-5760

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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