Chiral 1,2-Diols: The Assignment of Their Absolute Configuration by NMR Made Easy-Reference-Cited by-同舟云学术

Chiral 1,2-Diols: The Assignment of Their Absolute Configuration by NMR Made Easy

Published:2009-11-18 Issue:2 Volume:12 Page:208-211
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Freire Félix¹,Seco José Manuel¹,Quiñoá Emilio¹,Riguera Ricardo¹

Affiliation:

1. Departamento de Química Orgánica, Facultad de Química, and Unidad de RMN de Biomoléculas Asociada al CSIC, Universidad de Santiago de Compostela, 15782, Santiago de Compostela, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9021639

Reference12 articles.

1. The Assignment of Absolute Configuration by NMR

2. A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR

3. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

4. On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols

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