Determination of the enantiomeric excess of α-hydroxy acids-Reference-Cited by-同舟云学术

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Determination of the enantiomeric excess of α-hydroxy acids

Published:1993-01 Issue:12 Volume:4 Page:2495-2500
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Cavelier Florine,Gomez Sylvie,Jacquier Robert,Llinares Muriel,Mercadier Jean-Luc,Petrus Clément,Verducci Jean

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference32 articles.

1. NMR determination of enantiomeric purity

2. 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

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

4. Synthesis of (S)-(+)-2--butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid: A new type chiral derivation reagent for amines and alcohols

Cited by 13 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. Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses;Tetrahedron: Asymmetry;2009-02

2. Destruxin analogs: variations of the α-hydroxy acid side chain;The Journal of Peptide Research;2009-01-12

3. Chiral linker. Part 4: Diastereoselective addition of RZnX to α-keto esters using m-hydrobenzoin derived chiral auxiliaries in solution and on solid support and their application in the stereoselective synthesis of frontalin;Tetrahedron: Asymmetry;2006-09

4. Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters;Tetrahedron: Asymmetry;2006-09

5. Chiral linker. Part 2: Synthesis and evaluation of a novel, reusable solid-supported open chain chiral auxiliary derived from m-hydrobenzoin for the diastereoselective reduction of α-keto esters;Tetrahedron: Asymmetry;2005-10

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