1H and 13C NMR studies of some O‐carbamoyloximes

Mohammed I.M. Wazeer; Sk A. Ali; Mohammed Arab

doi:10.1002/mrc.1260271117

¹H and ¹³C NMR studies of some O‐carbamoyloximes

Mohammed I.M. Wazeer^*
, Sk A. Ali
, Mohammed Arab

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

Abstract

The ¹H and ¹³C NMR spectra were assigned for a series of O‐carbamoyloximes of ortho‐ and para‐substituted benzaldehyde. These compounds exist exclusively in the E configuration. The aromatic protons and carbons show correlations with the appropriate substituent‐induced shifts and with Hammett parameters.

Original language	English
Pages (from-to)	1102-1104
Number of pages	3
Journal	Magnetic Resonance in Chemistry
Volume	27
Issue number	11
DOIs	https://doi.org/10.1002/mrc.1260271117
State	Published - Nov 1989

Keywords

H and C NMR
Hammett parameters
O‐Carbamoyloximes

ASJC Scopus subject areas

General Chemistry
General Materials Science

Access to Document

10.1002/mrc.1260271117

Cite this

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title = "1H and 13C NMR studies of some O‐carbamoyloximes",

abstract = "The 1H and 13C NMR spectra were assigned for a series of O‐carbamoyloximes of ortho‐ and para‐substituted benzaldehyde. These compounds exist exclusively in the E configuration. The aromatic protons and carbons show correlations with the appropriate substituent‐induced shifts and with Hammett parameters.",

keywords = "H and C NMR, Hammett parameters, O‐Carbamoyloximes",

author = "Wazeer, \{Mohammed I.M.\} and Ali, \{Sk A.\} and Mohammed Arab",

year = "1989",

month = nov,

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T1 - 1H and 13C NMR studies of some O‐carbamoyloximes

AU - Wazeer, Mohammed I.M.

AU - Ali, Sk A.

AU - Arab, Mohammed

PY - 1989/11

Y1 - 1989/11

N2 - The 1H and 13C NMR spectra were assigned for a series of O‐carbamoyloximes of ortho‐ and para‐substituted benzaldehyde. These compounds exist exclusively in the E configuration. The aromatic protons and carbons show correlations with the appropriate substituent‐induced shifts and with Hammett parameters.

AB - The 1H and 13C NMR spectra were assigned for a series of O‐carbamoyloximes of ortho‐ and para‐substituted benzaldehyde. These compounds exist exclusively in the E configuration. The aromatic protons and carbons show correlations with the appropriate substituent‐induced shifts and with Hammett parameters.

KW - H and C NMR

KW - Hammett parameters

KW - O‐Carbamoyloximes

UR - https://www.scopus.com/pages/publications/84989094242

U2 - 10.1002/mrc.1260271117

DO - 10.1002/mrc.1260271117

M3 - Article

AN - SCOPUS:84989094242

SN - 0749-1581

VL - 27

SP - 1102

EP - 1104

JO - Magnetic Resonance in Chemistry

JF - Magnetic Resonance in Chemistry

IS - 11

ER -