Efficient 1H NMR chiral discrimination of sulfoxides caused by the dynamic nature of (R,R)-3′,3″-biBINOL-Reference-Cited by-同舟云学术

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Efficient 1H NMR chiral discrimination of sulfoxides caused by the dynamic nature of (R,R)-3′,3″-biBINOL

Published:2017-11 Issue:11 Volume:28 Page:1587-1590
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Kawanami Toshio,Ishizuka Kentaro,Furuno Hiroshi,Shiota Yoshihito,Yoshizawa Kazunari,Inanaga Junji

Funder

JSPS KAKENHI

The Japan Science Society

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference43 articles.

1. NMR determination of enantiomeric purity

2. Chiral reagents for the determination of enantiomeric excess and absolute configuration using NMR spectroscopy

3. Assignment of absolute configuration using chiral reagents and NMR spectroscopy

4. Determination of the chiral purity of aminoalcohols by 1H NMR spectroscopy

5. Chiral Recognition of Aminoalcohols by1H and13C NMR Spectroscopy using binaphthyl derivatives as chiral solvating agents

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1. Application of aromatic amide‐derived atropisomers as chiral solvating agents for discrimination of optically active mandelic acid derivatives in 1 H nuclear magnetic resonance spectroscopy;Magnetic Resonance in Chemistry;2021-06-15

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