Maximum likelihood constrained deconvolution. I: Algorithm and qualitative and quantitative enhancement in synthetic two-dimensional NMR spectra

2002 ◽  
Vol 14 (6) ◽  
pp. 402-415 ◽  
Author(s):  
Gwang-Woo Jeong ◽  
Heoung-Keun Kang
Keyword(s):  
Maximum Likelihood ◽  
Nmr Spectra ◽  
Two Dimensional ◽  
Qualitative And Quantitative

scholarly journals Deconvolution of Two-Dimensional NMR Spectra by Fast Maximum Likelihood Reconstruction: Application to Quantitative Metabolomics

2011 ◽  
Vol 83 (12) ◽  
pp. 4871-4880 ◽  
Author(s):  
Roger A. Chylla ◽  
Kaifeng Hu ◽  
James J. Ellinger ◽  
John L. Markley
Keyword(s):  
Maximum Likelihood ◽  
Nmr Spectra ◽  
Two Dimensional ◽  
Quantitative Metabolomics

Studies of the neutral trisaccharides of goat (Capra hircus) colostrum and of the one- and two-dimensional 1H and 13C NMR spectra of 6′-N-acetylglucosaminyllactose

1994 ◽  
Vol 262 (2) ◽  
pp. 173-184 ◽  
Author(s):  
Tadasu Urashima ◽  
William A. Bubb ◽  
Michael Messer ◽  
Yuhnagi Tsuji ◽  
Yasuko Taneda
Keyword(s):  
13C Nmr ◽  
Nmr Spectra ◽  
Capra Hircus ◽  
13C Nmr Spectra ◽  
Two Dimensional ◽  
1H And 13C Nmr ◽  
The One

scholarly journals Competitive Diels–Alder and ene addition of N-arylmaleimides to 7-dehydrocholesteryl acetate

1992 ◽  
Vol 70 (11) ◽  
pp. 2730-2744 ◽  
Author(s):  
William J. Leigh ◽  
Donald W. Hughes ◽  
D. Scott Mitchell
Keyword(s):  
Molecular Mechanics ◽  
Nmr Spectra ◽  
Benzene Solution ◽  
Diels Alder ◽  
Spectroscopic Techniques ◽  
Two Dimensional ◽  
A Minor ◽  
C Nmr ◽  
Alder Adduct ◽  
Ene Addition

Thermolysis of N-phenyl, N-para-biphenyl, and N-para, para′-terphenylmaleimide with 7-dehydrocholesteryl acetate in benzene solution at 200 °C yields mixtures of four cycloadducts in relative yields that are essentially independent of the maleimide substituent. The three major products are those of ene addition to C7 of the steroid with abstraction of the proton at C9 or C14. The α-endo-Diels-Alder adduct is formed as a minor product. The structures of the adducts have been elucidated on the basis of one- and two-dimensional 1H and 13C NMR spectroscopic techniques, including homonuclear 1H decoupling, NOE, 1H–1H COSY, heteronuclear 1H–13C shift correlation, and TOCSY 2-D experiments, and the results of molecular mechanics (MMX) calculations. The combination of these techniques has made it possible to almost completely assign the 1H and 13C NMR spectra for two of the ene adducts and the Diels–Alder adduct from reaction of 7-dehydrocholesteryl acetate with N-phenyl maleimide.

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