1H and 13C NMR studies of 2-functionalized 5-(methylsulfonyl)-1-phenyl-1H-indoles

The 1H and 13C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1H‐indoles were assigned completely and unequivocally using the concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐HMQC and gs‐HMBC). Finally, the influence of the 2‐substituent of 5‐(methylsufo...

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Published inMagnetic resonance in chemistry Vol. 45; no. 2; pp. 185 - 188
Main Authors Cruz-López, Olga, Gallo, Miguel A., Espinosa, Antonio, Campos, Joaquín M.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.02.2007
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Abstract The 1H and 13C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1H‐indoles were assigned completely and unequivocally using the concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐HMQC and gs‐HMBC). Finally, the influence of the 2‐substituent of 5‐(methylsufonyl)‐1‐phenyl‐1H‐indoles on the carbon atoms of the indole moiety was estimated. Copyright © 2006 John Wiley & Sons, Ltd.
AbstractList The 1H and 13C NMR resonances of thirty 2-functionalized 5-(methylsulfonyl)-1-phenyl-1H-indoles were assigned completely and unequivocally using the concerted application of one- and two-dimensional experiments (DEPT, gs-HMQC and gs-HMBC). Finally, the influence of the 2-substituent of 5-(methylsufonyl)-1-phenyl-1H-indoles on the carbon atoms of the indole moiety was estimated.
The 1H and 13C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1H‐indoles were assigned completely and unequivocally using the concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐HMQC and gs‐HMBC). Finally, the influence of the 2‐substituent of 5‐(methylsufonyl)‐1‐phenyl‐1H‐indoles on the carbon atoms of the indole moiety was estimated. Copyright © 2006 John Wiley & Sons, Ltd.
Author Espinosa, Antonio
Campos, Joaquín M.
Cruz-López, Olga
Gallo, Miguel A.
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References Wilker W, Leibfritz D, Kerssebaum R, Bermel W. Magn. Reson. Chem. 1993; 31: 287.
(c) Gribble GW. J. Chem. Soc., Perkin Trans. 1 2000; 1045.
Campos JM, Sánchez-Martín RM, Cruz-López O, Conejo-García A, Gallo MA, Espinosa A. Magn. Reson. Chem. 2005; 43: 1066.
Hurd RE, John BK. J. Magn. Reson. 1991; 91: 648.
Palomer A, Cabré F, Pascual J, Campos J, Trujillo MA, Entrena A, Gallo MA, García L, Mauleón D, Espinosa A. J. Med. Chem. 2002; 45: 1402.
Marnett LJ, Kalgutkar AM. Curr. Opin. Chem. Biol. 1998; 2: 482.
Cruz-López O, Díaz-Mochón JJ, Campos JM, Entrena A, Núñez MT, Labeaga L, Orjales A, Gallo MA, Espinosa A. ChemMedChem (in press).
Campos J, Díaz JJ, Núñez MC, Entrena A, Gallo MA, Espinosa A. Magn. Reson. Chem. 2002; 40: 554.
Rodrigues CR, Veloso MP, Verli H, Fraga CAM, Miranda ALP, Barreiro EF. Curr. Med. Chem. 2002; 9: 849.
(a) Sundberg RJ. Indoles. Academic Press: San Diego, CA, 1996
Campos Rosa J, Galanakis D, Ganellin CR. Magn. Reson. Chem. 1998; 36: 951.
Pineda de las Infantas MJ, Campos J, Baraldi PG, Romagnoli R, Gallo MA, Espinosa A. Magn. Reson. Chem. 2003; 41: 478.
2005; 43
1991; 91
1998; 2
2002; 9
1996 2000 2000; 10
2002; 40
2003; 41
2002; 45
1998; 36
1993; 31
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  start-page: 951
  year: 1998
  publication-title: Magn. Reson. Chem.
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  year: 2002
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  year: 2002
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  publication-title: Magn. Reson. Chem.
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  year: 1998
  publication-title: Curr. Opin. Chem. Biol.
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  start-page: 478
  year: 2003
  publication-title: Magn. Reson. Chem.
– volume: 40
  start-page: 554
  year: 2002
  publication-title: Magn. Reson. Chem.
– volume: 43
  start-page: 1066
  year: 2005
  publication-title: Magn. Reson. Chem.
– volume: 91
  start-page: 648
  year: 1991
  publication-title: J. Magn. Reson.
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Snippet The 1H and 13C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1H‐indoles were assigned completely and unequivocally using the concerted...
The 1H and 13C NMR resonances of thirty 2-functionalized 5-(methylsulfonyl)-1-phenyl-1H-indoles were assigned completely and unequivocally using the concerted...
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SubjectTerms 13C NMR
1H NMR
2D NMR
5-(methylsulfonyl)-1-phenyl-1H-indoles
Carbon Isotopes
HMBC
HMQC
Hydrogen
Indoles - chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
NMR
Title 1H and 13C NMR studies of 2-functionalized 5-(methylsulfonyl)-1-phenyl-1H-indoles
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