New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds-Reference-Cited by-同舟云学术

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New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds

Published:1994-06 Issue:25 Volume:35 Page:4397-4400
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kusumi Takenori,Takahashi Haruko,Xu Ping,Fukushima Toshiro,Asakawa Yoshinori,Hashimoto Toshihiro,Kan Yukiko,Inouye Yoshinobu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 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. Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives

3. On the stereochemistry of the bis-nor-wieland-miescher ketome

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

5. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

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2. Methods and Application of Absolute Configuration Assignment for Chiral Compounds;Chinese Journal of Organic Chemistry;2022

3. Methods for determining the absolute configurations of marine ladder‐shaped polyethers;Chirality;2020-02-17

4. Total Synthesis of a Simplest Natural Product by a Clumsy Chemist;Journal of Synthetic Organic Chemistry, Japan;2019-06-01

5. 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;Organic & Biomolecular Chemistry;2019

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