scholarly journals Nuclear Magnetic Resonance Spectra of Amino Acids and their Derivatives. II. Analyses of NMR Spectra of Amino Acids

1963 ◽  
Vol 36 (5) ◽  
pp. 578-579 ◽  
Author(s):  
Shizuo Fujiwara ◽  
Yoji Arata
Keyword(s):  
Amino Acids ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The metal nuclear magnetic resonance spectra of some tin(II) and lead(II) complexes with polydentate phosphines

1983 ◽  
Vol 61 (8) ◽  
pp. 1795-1799 ◽  
Author(s):  
Philip A. W. Dean
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Narrow Range ◽  
Chemical Shifts ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The previously reported 1:1 complexes formed in MeNO2, between M(SbF6)2 (M = Sn or Pb) and Ph2P(CH2)2PPh2, PhP[(CH2)2PPh2]2, MeC(CH2PPh2)3, P[(CH2)2PPh2]3, and [Formula: see text] have been studied by metal (119Sn or 207Pb) nmr. The metal chemical shifts span the comparatively narrow range of −586 to −792 ppm and 60 to −269 ppm, relative to the resonance of MMe4, for 119Sn and 207Pb nmr, respectively. The implications of these data regarding the denticity of the ligand in M(P[(CH2)2PPh2]3)2+ are discussed, and a comparison with the metal nmr spectra of related stannous and plumbous complexes is made.

A correction in the published nuclear magnetic resonance spectra of trans-camphane-2,3-diols

1979 ◽  
Vol 57 (3) ◽  
pp. 318-319 ◽  
Author(s):  
Mark A. Johnson ◽  
Michael P. Fleming
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Silyl Ether ◽  
Endo Isomer ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

It is unequivocally shown that the published nmr spectra assigned to 2-endo,3-exo-camphanediol and 2-exo-3-endo-camphanediol should be reversed. The 2-exo,3-endo isomer is prepared unambiguously by hydroboration–oxidation of camphor enol silyl ether.

scholarly journals Carbon-13 nuclear magnetic resonance spectra of oxazoles

1979 ◽  
Vol 57 (23) ◽  
pp. 3168-3170 ◽  
Author(s):  
Henk Hiemstra ◽  
Hendrik A. Houwing ◽  
Okko Possel ◽  
Albert M. van Leusen
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
Coupling Constants ◽  
Proton Coupling ◽  
Nuclear Magnetic Resonance Spectra ◽  
C Nmr ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The 13C nmr spectra of oxazole and eight mono- and disubstituted derivatives have been analyzed with regard to the chemical shifts and the various carbon–proton coupling constants of the ring carbons. The data of the parent oxazole are compared with thiazole and 1-methylimidazole.

11B—NMR- spektroskopische Untersuchungen an wäßrigen Polyboratlösungen / 11B NMR Spectroscopic Studies on Aqueous Polyborate Solutions

1979 ◽  
Vol 34 (8) ◽  
pp. 1078-1083 ◽  
Author(s):  
Ralf Janda ◽  
Gert Heller
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Aqueous Solutions ◽  
Nmr Spectra ◽  
Spectroscopic Studies ◽  
Sodium Potassium ◽  
Nuclear Magnetic Resonance Spectra ◽  
11B Nmr ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The 11B nuclear magnetic resonance spectra of sodium, potassium and ammonium polyborates in aqueous solutions, - as a function of concentration and pH - , provide information of the hydrolysis equilibria. Two 11B NMR lines are observed in aqueous solutions of Na[B5O6(OH)4], K[B5O6(OH)4] and NH4[B5O6(OH)4]. Only one 11B NMR line is recorded in aqueous solutions of (NH4)2[B4O5(OH)4] and Na2[B4O5(OH)4]. The results of the 11B NMR spectra are discussed and compared with the results obtained from Raman studies of aqueous polyborate solutions

Use of a bacteriophage to depolymerize a polysaccharide to an oligosaccharide; comparison of the 1H and 13C nuclear magnetic resonance spectra of the polymer and its hexasaccharide repeating unit

1980 ◽  
Vol 58 (23) ◽  
pp. 2588-2591 ◽  
Author(s):  
Guy G. S. Dutton ◽  
Angela V. Savage ◽  
Michel Vignon
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Capsular Polysaccharide ◽  
Nuclear Magnetic Resonance Spectra ◽  
13C Nuclear Magnetic Resonance ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

A β-D-galactosidase associated with bacteriophage [Formula: see text] has been used to depolymerize the capsular polysaccharide of Klebsiella serotype K18 into the hexasaccharide corresponding to one repeating unit of the polymer. The nmr spectra of the polymer and of the oligosaccharide are comparable, leading to the conclusion that the conformations in solution of the repeating unit of the two substances are similar.

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