Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the  13 C chemical shifts with the aid of deuterated derivatives | Zendy

Seita José | Zendy; Sandström Jan | Zendy; Drakenberg Torbjörn | Zendy

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Carbon‐13 NMR studies of substituted naphthalenes. I—complete assignments of the 13 C chemical shifts with the aid of deuterated derivatives

Author(s) -

Seita José,

Sandström Jan,

Drakenberg Torbjörn

Publication year - 1978

Publication title -

organic magnetic resonance

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0030-4921

DOI - 10.1002/mrc.1270110505

Subject(s) - deuterium , chemical shift , chemistry , proton , deuterium nmr , carbon 13 nmr , spectral line , nmr spectra database , coupling (piping) , computational chemistry , stereochemistry , materials science , physics , nuclear physics , astronomy , metallurgy

Proton‐coupled as well as noise‐decoupled 13 C NMR spectra of several substituted naphthalenes have been studied. Complete assignments of the 13 C signals based on selectively deuterated derivatives and on the 13 C 1 H coupling pattern have been made. For the methoxynaphthalenes, acetylnaphthalenes and naphthaldehydes the dominant conformations of the substituents have been deduced from the 13 C chemical shifts.

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