Premium
Die Amid‐Iminol‐Tautomerie
Author(s) -
Grob C. A.,
Fischer B.
Publication year - 1955
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19550380716
Subject(s) - chemistry , tautomer , amide , medicinal chemistry , stereochemistry , organic chemistry
Abstract The prevailing uncertainty regarding the predominant tautomer in cases of potential amide‐iminol (lactam‐lactim) tautomerism is attributable mainly to the finding that the ultra violet absorption of certain amides resembles that of corresponding imino ethers more closely than that of N, N‐disubstituted amides.