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Abstract 15N and 13C chemical shifts and the 1J(15N15N), 1J(15N13C) and 1J(13CH) coupling constants have been determined for a number of 15N‐enriched cyclic and acyclic secondary nitramines. The results are interpreted in terms of both electronegativity effects and conformational factors.
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Bulusu et al. (1981) studied this question.
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