1H and 13C NMR spectral assignments of 2′‐hydroxychalcones. (17th April 2013)

• Record Type: Journal Article
• Authors: Yong, Yeonjoong; Ahn, Seunghyun; Hwang, Doseok; Yoon, Hyuk; Jo, Geunhyeong; Kim, Young Hwa; Kim, Sang Ho; Koh, Dongsoo; Lim, Yoongho
• Is Part Of: Magnetic resonance in chemistry. Volume 51:Number 6(2013:Jun.)
• Page Start: 364
• Page End: 370
• Publication Date: 2013-04-17
• Subjects: Nuclear magnetic resonance spectroscopy -- Periodicals; Chemistry, Organic -- Periodicals; Magnetic resonance -- Periodicals; 538.36
• DOI: 10.1002/mrc.3949
• Languages: English
• ISSNs: 0749-1581

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Chalcones are of interest to medicinal chemists because their structures can be easily modified with various functional groups. The syntheses and biological activities of chalcones from natural sources are well known. In this study, 24 2′‐hydroxychalcones bearing methoxy substituents were synthesized, among which five are new. The NMR data for all synthesized chalcones are described for the first time. The complete assignments of the ¹H and ¹³C NMR data can be used for the identification of newly discovered and widely isolated, synthesized chalcones. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract>