Resolution of isoborneol and its isomers by GC/MS to identify "synthetic" and "semi‐synthetic" borneol products.
- Published in:
- Chirality, 2018, v. 30, n. 11, p. 1233, doi. 10.1002/chir.23017
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- Publication type:
- Article
Works matching IS 08990042 AND DT 2018 AND VI 30 AND IP 11
Results: 8
1
2
The enzymatic resolution of 1‐(4‐chlorophenyl)ethylamine by Novozym 435 to prepare a novel triazolopyrimidine herbicide.
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- Chirality, 2018, v. 30, n. 11, p. 1225, doi. 10.1002/chir.23016
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- Article
3
Stereoselective conjugate addition of ketones to alkylidene malonates using thiourea‐sulfonamide organocatalyst.
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- Chirality, 2018, v. 30, n. 11, p. 1215, doi. 10.1002/chir.23015
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- Article
4
Absolute configurations of chiral molecules with multiple stereogenic centers without prior knowledge of the relative configurations: A case study of inuloxin C.
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- Chirality, 2018, v. 30, n. 11, p. 1206, doi. 10.1002/chir.23013
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- Article
5
Box‐Behnken response surface modeling assisted enantiomeric resolution of some racemic β‐blockers using HPTLC and β‐cyclodextrin as chiral mobile phase additive: Application to check the enantiomeric purity of betaxolol.
- Published in:
- Chirality, 2018, v. 30, n. 11, p. 1195, doi. 10.1002/chir.23012
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- Article
6
Complex‐precipitation using functionalized chiral ionic liquids with L‐proline anion and chromatographic analysis for enantioseparation of racemic amino acids.
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- Chirality, 2018, v. 30, n. 11, p. 1182, doi. 10.1002/chir.23011
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- Article
7
Chiral recognition of the carnitine enantiomers using rhodamine B as a resonance Rayleigh scattering probe.
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- Chirality, 2018, v. 30, n. 11, p. 1173, doi. 10.1002/chir.23004
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- Article
8
Issue Information.
- Published in:
- Chirality, 2018, v. 30, n. 11, p. 1169, doi. 10.1002/chir.22762
- Publication type:
- Article