ChemInform Abstract: TOTAL ASSIGNMENT OF THE CARBON-13 NMR SPECTRA OF 5H-INDOLO(1,7-AB)(1)BENZAZEPINE AND 6,7-DIHYDRO-5H-INDOLO(1,7-AB)(1)BENZAZEPINE USING TWO-DIMENSIONAL PROTON-CARBON CHEMICAL SHIFT CORRELATION EXPERIMENTS

1985 ◽  
Vol 16 (29) ◽  
Author(s):  
A. HALLBERG ◽  
A. R. MARTIN ◽  
G. E. MARTIN ◽  
G. GROENBERG
Keyword(s):  
Chemical Shift ◽  
Nmr Spectra ◽  
Two Dimensional ◽  
Chemical Shift Correlation ◽  
Carbon Chemical Shift

Total assignment of the carbon-13 NMR spectrum of the cembranoid diterpene eunicin through the use of two-dimensional proton-carbon chemical shift correlation

1984 ◽  
Vol 106 (6) ◽  
pp. 1823-1826 ◽  
Author(s):  
Robert T. Gampe ◽  
Maktoob Alam ◽  
Alfred J. Weinheimer ◽  
Gary E. Martin ◽  
James A. Matson ◽  
...  
Keyword(s):  
Chemical Shift ◽  
Two Dimensional ◽  
Chemical Shift Correlation ◽  
Nmr Spectrum ◽  
Carbon Chemical Shift

ChemInform Abstract: Long Range Optimized Two-Dimensional Proton-Carbon Chemical Shift Correlation.

1986 ◽  
Vol 17 (19) ◽  
Author(s):  
M. J. QUAST ◽  
E. L. EZELL ◽  
G. E. MARTIN ◽  
M. L. LEE ◽  
M. L. TEDJAMULIA ◽  
...  
Keyword(s):  
Chemical Shift ◽  
Long Range ◽  
Two Dimensional ◽  
Chemical Shift Correlation ◽  
Carbon Chemical Shift

scholarly journals Notizen: High-field (500 MHz) 1H NMR Spectra of Retinoic Acids and Arotinoids by Two-dimensional Chemical Shift Correlation (2D) Spectroscopy

1988 ◽  
Vol 43 (8) ◽  
pp. 1072-1074 ◽  
Author(s):  
Bruno Perly ◽  
Giuseppe C. Pappalardo ◽  
Michael Klaus ◽  
Enzo Montoneri
Keyword(s):  
Chemical Shift ◽  
Nmr Spectra ◽  
Chair Conformation ◽  
Two Dimensional ◽  
Trans Isomers ◽  
Chemical Shift Correlation ◽  
H Nmr ◽  
Retinoic Acids ◽  
Cis And Trans Isomers ◽  
Cis And Trans

AbstractThe 1H NMR spectra (in DMSO solution at 300 K) of retinoic acids (cis- and trans-isomers) and new arotinoids were run at 500 MHz and assigned by using homo- and heteronuclear two-dimensional (2D) chemical shift correlation experiments. Spectral analysis was indicating, on the basis of 7 values, that the ring C(l)-C(2)-C(3)-C(4)-C(5)-C(6) adopts, in all compounds, a chair conformation.

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