Enantioresolution of 2-methoxy-2-(1-naphtyl)propionic acid using diastereomeric salt formation with chiral phenylethylamine-Reference-Cited by-同舟云学术

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Enantioresolution of 2-methoxy-2-(1-naphtyl)propionic acid using diastereomeric salt formation with chiral phenylethylamine

Published:2014-07 Issue:30 Volume:55 Page:4114-4116
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kusakari Miho,Ohta Yurie,Nakagawa Hideaki,Katagiri Hiroshi,Kijima Tatsuro,Murakami Satoshi,Matsuba Shigeru,Hatano Bunpei

Funder

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

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

2. Chiral reagents for the determination of enantiomeric excess and absolute configuration using NMR spectroscopy

3. A new and simple synthesis of Mosher's acid

4. 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

5. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. New Advances in the Synthetic Application of Enantiomeric 1-Phenylethylamine (α-PEA): Privileged Chiral Inducer and Auxiliary;Molecules;2020-10-23

2. Application of the modified 2-methoxy-2-(1-naphthyl)propionic (MαNP) acid method to steroidal alcohols and the most efficient HPLC separation found in diastereomeric MαNP esters;Tetrahedron: Asymmetry;2015-04

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