Assignment of Absolute Configuration of Natural Abundance Deuterium Signals Associated with (R)- and (S)-Enantioisotopomers in a Fatty Acid Aligned in a Chiral Liquid Crystal: Enantioselective Synthesis and NMR Analysis-Reference-Cited by-同舟云学术

Assignment of Absolute Configuration of Natural Abundance Deuterium Signals Associated with (R)- and (S)-Enantioisotopomers in a Fatty Acid Aligned in a Chiral Liquid Crystal: Enantioselective Synthesis and NMR Analysis

Published:2006-08-01 Issue:34 Volume:128 Page:11180-11187
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Baillif Vincent¹,Robins Richard J.¹,Billault Isabelle¹,Lesot Philippe¹

Affiliation:

1. Contribution from the Laboratoire d'Analyse Isotopique et Electrochimique de Métabolismes, CNRS UMR 6006, Université de Nantes, BP 92208, 44322 Nantes, France, and Laboratoire de Chimie Structurale Organique, CNRS UMR 8182, ICMMO, Bât. 410, Université de Paris-Sud, 91405 Orsay Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0617892

Reference45 articles.

1. Formation of conjugated Δ11Δ13-double bonds by Δ12-linoleic acid (1,4)-acyl-lipid-desaturase in pomegranate seeds

2. Bioorganic chemistry of plant lipid desaturation

3. Deuterium labelling at the natural abundance level as studied by high field quantitative 2H NMR

4. Deuterium transfer in the bioconversion of glucose to ethanol studied by specific labeling at the natural abundance level

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