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Applied Spectroscopy

Applied Spectroscopy

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  • Vol. 40, Iss. 3 — Mar. 1, 1986
  • pp: 369–373

Carbon13 NMR Shift Assignments for E- and Z-Dothiepin Hydrochloride and 6H-Dibenzo[b,e]thiepin-11-One

Dorothy K. Wyatt, Nina Matheny Roscher, and Lee T. Grady

Applied Spectroscopy, Vol. 40, Issue 3, pp. 369-373 (1986)


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Abstract

Carbon13 chemical shift assignments are reported for Z- and E-dothiepin hydrochloride (N,N-dimethyldibenzo[b,e]thiepin-delta-11(6H)', gamma-propylamine hydrochloride). The commercial product, a mixture of approximately 95% E-isomer, is of clinical importance as an antide-pressant drug. The precursor and degradation product, 6H-dibenzo[b,e]thiepin-11-one, and related model compounds were also studied. Homo- and heteronuclear shift-correlated 2D NMR, selective INEPT, selective and off-resonance decoupling, and inversion-recovery (T1) experiments as well as model compound comparisons were used in assignments.

Citation
Dorothy K. Wyatt, Nina Matheny Roscher, and Lee T. Grady, "Carbon13 NMR Shift Assignments for E- and Z-Dothiepin Hydrochloride and 6H-Dibenzo[b,e]thiepin-11-One," Appl. Spectrosc. 40, 369-373 (1986)
http://www.opticsinfobase.org/as/abstract.cfm?URI=as-40-3-369

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