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Chiral derivatizing agent (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Chiral derivatizing agent" in English language version.

refsWebsite
Global rank English rank
12doi.org
2nd place
2nd place
1harvard.edu
18th place
17th place
1umn.edu
1,266th place
860th place
1archive.today
14th place
14th place
1bioinfo.pl
low place
low place
1nih.gov
4th place
4th place

archive.today

bioinfo.pl

lib.bioinfo.pl

doi.org

  • J. L. Mateos and D. J. Cram (1959). "Studies in Stereochemistry. XXXI. Conformation, Configuration and Physical Properties of Open-chain Diastereomers". J. Am. Chem. Soc. 81 (11): 2756–2762. Bibcode:1959JAChS..81.2756M. doi:10.1021/ja01520a037.
  • J. A. Dale, D. L. Dull and H. S. Mosher (1969). "α-Methoxy-α-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines". J. Org. Chem. 34 (9): 2543–2549. doi:10.1021/jo01261a013.
  • D. Parker (1991). "NMR determination of enantiomeric purity". Chem. Rev. 91 (7): 1441–1457. doi:10.1021/cr00007a009.
  • Pirkle, W. H.; J. R. Hauske (1977). "Broad spectrum methods for the resolution of optical isomers. A discussion of the reasons underlying the chromatographic separability of some diastereomeric carbamates". J. Org. Chem. 42 (11): 1839. doi:10.1021/jo00431a004.
  • Helmchen, G.; K. Sauber; R. Ott (1972). "Gezielte Trennung und absolute Konfiguration von enantiomeren Carbonsäuren und Aminen (1. Mitteilung) Günter Helmchen". Tetrahedron Letters. 13 (37): 3873. doi:10.1016/s0040-4039(01)94184-x.
  • Helmchen, G.; G. Nill; D. Flockerzi; W. Schuhle; M.S.K. Youssef (1979). "Preparative Scale Directed Resolution of Enantiomeric Aminesvia Liquid Chromatography of Diastereomeric 4-Hydroxybutyramides". Angew. Chem. Int. Ed. Engl. 18 (1): 62. doi:10.1002/anie.197900651.
  • Pirkle, W. H.; J. R. Hauske (1977). "Design of chiral derivatizing agents for the chromatographic resolution of optical isomers. Asymmetric synthesis of some chiral fluoroalkylated amines". J. Org. Chem. 42 (14): 2436. doi:10.1021/jo00434a019.
  • Pirkle, W.H.; P.L. Rinaldi (1979). "Synthesis and enantiomeric purity determination of the optically active epoxide disparlure, sex pheromone of the gypsy moth". J. Org. Chem. 44 (7): 1025. doi:10.1021/jo01321a001.
  • Blaschke, G. (1980). "Chromatographic Resolution of Racemates. New analytical methods (17)". Angew. Chem. Int. Ed. Engl. 19 (1): 13. doi:10.1002/anie.198000131.
  • J. M. Seco; E. Quiñoá; R. Riguera* (June 2012). "Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents". Chemical Reviews. 112 (8): 4603–4641. doi:10.1021/cr2003344. PMID 22658125.
  • Sastri, V.S; Bünzli, Jean-Claude; Rao, V. Ramachandra; Rayudu, G.V.S; Perumareddi, J.R (2003). "Lanthanide Nmr Shift Reagents". Modern Aspects of Rare Earths and Their Complexes. pp. 779–843. doi:10.1016/B978-044451010-5/50024-9. ISBN 9780444510105.
  • Katarzyna M. Błażewskaa; Tadeusz Gajda (July 2009). "Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy". Tetrahedron: Asymmetry. 20 (12): 1337–1361. doi:10.1016/j.tetasy.2009.05.021.

harvard.edu

ui.adsabs.harvard.edu

  • J. L. Mateos and D. J. Cram (1959). "Studies in Stereochemistry. XXXI. Conformation, Configuration and Physical Properties of Open-chain Diastereomers". J. Am. Chem. Soc. 81 (11): 2756–2762. Bibcode:1959JAChS..81.2756M. doi:10.1021/ja01520a037.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • J. M. Seco; E. Quiñoá; R. Riguera* (June 2012). "Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents". Chemical Reviews. 112 (8): 4603–4641. doi:10.1021/cr2003344. PMID 22658125.

umn.edu

chem.umn.edu