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
Subjects
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
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Summary: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.
Bibliography:FAES S. A., [Leioa (Bilbao), Spain] - No. F1852
istex:D54D9B1302133A6F1A517093A06ED4C63E9ED134
ark:/67375/WNG-TSDM4H01-9
ArticleID:MRC1935
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0749-1581
1097-458X
DOI:10.1002/mrc.1935