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

CruzLópez Olga | Zendy; Gallo Miguel A. | Zendy; Espinosa Antonio | Zendy; Campos Joaquín M. | Zendy

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

Author(s) -

CruzLópez Olga,

Gallo Miguel A.,

Espinosa Antonio,

Campos Joaquín M.

Publication year - 2007

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.1935

Subject(s) - chemistry , dept , substituent , moiety , indole test , carbon 13 nmr , proton nmr , stereochemistry , medicinal chemistry

The 1 H and 13 C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1 H ‐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‐1 H ‐indoles on the carbon atoms of the indole moiety was estimated. Copyright © 2006 John Wiley & Sons, Ltd.

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