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Mendeleev Communications, 2010, Volume 20, Issue 2, Pages 104–105
DOI: https://doi.org/10.1016/j.mencom.2010.03.013
(Mi mendc3004)
 

This article is cited in 6 scientific papers (total in 6 papers)

Cinchona alkaloid ester derivatives as ligands in the asymmetric dihydroxylation and aminohydroxylation of alkenes

H. Chena, Q. Wanga, X. Suna, J. Luob, R. Jianga

a Department of Chemistry, Fourth Military Medical University, Xi'an, China
b Shannxi Institute for Food and Drug Control, Xi'an, China
Abstract: Cinchona alkaloid ester derivatives were adopted to asymmetric dihydroxylation and asymmetric aminohydroxylation reactions in excellent yields and enantiomeric excesses.
Keywords: cinchona alkaloids, asymmetric dihydroxylation (AD); asymmetric aminohydroxylation (AA); chiral; ester derivatives.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.1 Mb)


Citation: H. Chen, Q. Wang, X. Sun, J. Luo, R. Jiang, “Cinchona alkaloid ester derivatives as ligands in the asymmetric dihydroxylation and aminohydroxylation of alkenes”, Mendeleev Commun., 20:2 (2010), 104–105
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  • https://www.mathnet.ru/eng/mendc3004
  • https://www.mathnet.ru/eng/mendc/v20/i2/p104
  • This publication is cited in the following 6 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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