Chiral Recognition of N -Phthaloyl, N -Tetrachlorophthaloyl, and N -Naphthaloyl α-Amino Acids and Their Esters on Polysaccharide-Derived Chiral Stationary Phases-Reference-Cited by-同舟云学术

Chiral Recognition of N -Phthaloyl, N -Tetrachlorophthaloyl, and N -Naphthaloyl α-Amino Acids and Their Esters on Polysaccharide-Derived Chiral Stationary Phases

Published:2012-07-31 Issue:12 Volume:24 Page:1037-1046
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Kim Byoung-Hyoun¹,Lee Sang Uck¹,Moon Dong Cheul²

Affiliation:

1. Analytical Science, LG Chem. Research Park; LG Chem. Ltd.; Yusong-Gu Daejeon South Korea

2. College of Pharmacy; Chungbuk National University; Heungduk-Gu Cheongju South Korea

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.22094/fullpdf

Reference28 articles.

1. Application of chiral derivatizing agents in the high-performance liquid chromatographic separation of amino acid enantiomers: a review;Ilisz;J Pharm Biomed Anal,2008

2. High-performance liquid chromatographic separation of stereoisomers of N-phthaloyl protected amino acids and dipeptidomimetics;Ilisz;J Sep Sci,2007

3. Drug synthesis methods and manufacturing technology: synthesis of N-phthaloyl derivatives of amino acids;Zavyalov;Pharm Chem J,2002

4. Efficient microwave-assisted synthesis of 4-amino-2-benzazepin-3-ones as conformationally restricted dipeptide mimetics;Severino;Tetrahedron,2009

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