1 H,  13 C NMR studies of new 3‐aminophenol isomers linked to pyridinium salts | Zendy

SchiaffinoOrtega Santiago | Zendy; Espinosa Antonio | Zendy; Gallo Miguel A. | Zendy; LópezCara L. Carlota | Zendy; Entrena Antonio | Zendy

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1 H, 13 C NMR studies of new 3‐aminophenol isomers linked to pyridinium salts

Author(s) -

SchiaffinoOrtega Santiago,

Espinosa Antonio,

Gallo Miguel A.,

LópezCara L. Carlota,

Entrena Antonio

Publication year - 2013

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.4025

Subject(s) - chemistry , pyridinium , dept , moiety , nitro , heteronuclear single quantum coherence spectroscopy , pyridinium compounds , ring (chemistry) , carbon 13 nmr , butane , stereochemistry , proton nmr , medicinal chemistry , nuclear magnetic resonance spectroscopy , organic chemistry , catalysis , alkyl

1 H and 13 C NMR spectroscopic data of 20 new non‐symmetrical compounds were assigned by a combination of 1D and 2D NMR experiments (DEPT, HSQC, and HMBC). These compounds contain a 4‐( N , N ‐dimethylamino)‐ or 4‐(pyrrolidin‐1‐yl)pyridinium moiety and a 3‐nitro‐, 3‐amino‐, or 3‐hydroxyphenyl ring, linked by p ‐xylene, 4,4′‐dimethylbiphenyl, 1,2‐bis( p ‐tolyl)ethane, or 1,4‐bis( p ‐tolyl)butane. Copyright © 2013 John Wiley & Sons, Ltd.

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