Monosaccharides as Potential Chiral Probes for the Determination of the Absolute Configuration of Secondary Alcohols-Reference-Cited by-同舟云学术

Monosaccharides as Potential Chiral Probes for the Determination of the Absolute Configuration of Secondary Alcohols

Published:2016-10-26 Issue:11 Volume:79 Page:2797-2804
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Laskowski Tomasz¹,Szwarc Katarzyna¹,Szczeblewski Paweł¹,Sowiński Paweł¹,Borowski Edward¹,Pawlak Jan¹

Affiliation:

1. Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, Gabriela Narutowicza Street 11/12, 80-233 Gdańsk, Poland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.6b00471

Reference36 articles.

1. 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

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

3. Tetra-O-benzoylglucosylation: A New 1H Nuclear Magnetic Resonance Method for Determination of the Absolute Configuration of Secondary Alcohols

4. 2-Methoxy-2-(1-naphthyl)propionic acid, a powerful chiral auxiliary for enantioresolution of alcohols and determination of their absolute configurations by the 1H NMR anisotropy method

5. The Assignment of Absolute Configuration by NMR

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