Synthesis and characterization of novel chiral derivatizing agents containing β-keto-anthracene adducts (KAAs) by 1H-NMR: aromatic influence and chiral alcohol absolute configuration determination-Reference-Cited by-同舟云学术

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Synthesis and characterization of novel chiral derivatizing agents containing β-keto-anthracene adducts (KAAs) by 1H-NMR: aromatic influence and chiral alcohol absolute configuration determination

Published:2019 Issue:3 Volume:17 Page:541-554
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Intakaew Neeranuth¹²³⁴⁵,Rithchumpon Puracheth¹²³⁴⁵,Prommin Chanatkran¹²³⁴⁵,Yimklan Saranphong¹²³⁴⁵,Kungwan Nawee¹²³⁴⁵^ORCID,Thavornyutikarn Praput¹²³⁴⁵^ORCID,Meepowpan Puttinan¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. Faculty of Science

3. Chiang Mai University

4. Chiang Mai 50200

5. Thailand

Abstract

New chiral derivatizing agents and the effect of aromatic rings were investigated for absolute configuration of chiral alcohols via¹H-NMR.

Funder

National Research Council of Thailand

Faculty of Science, Chiang Mai University

Graduate School, Chiang Mai University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB02662A

Reference79 articles.

1. Stereochemistry in Drug Action

2. Pharmacodynamic and pharmacokinetic differences between drug enantiomers in humans: An overview

3. Pharmacological Importance of Stereochemical Resolution of Enantiomeric Drugs

4. Determination of absolute configurations by X-ray crystallography and1H NMR anisotropy

5. Absolute Configuration of Bromochlorofluoromethane from Experimental and Ab Initio Theoretical Vibrational Raman Optical Activity

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1. The Assignment of the Absolute Configuration of β-Chiral Primary Alcohols with Axially Chiral Trifluoromethylbenzimidazolylbenzoic Acid;The Journal of Organic Chemistry;2020-09-03

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