Literature DB >> 15128249

The asymmetric power of chiral ligands determined by competitive asymmetric autocatalysis.

François Lutz1, Itaru Sato, Kenso Soai.   

Abstract

Asymmetric autocatalytic reactions were initiated by using two competing chiral ligands bearing opposite configurations. The absolute configuration of the resulting highly enantioenriched product reflects the different efficiencies of the two catalysts. Thus, our method provides a simple and efficient way to compare the asymmetric power of chiral ligands for enantioselective catalysis both qualitatively and quantitatively.

Year:  2004        PMID: 15128249     DOI: 10.1021/ol049559k

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Isotope chirality and asymmetric autocatalysis: a possible entry to biological chirality.

Authors:  Béla Barabás; Luciano Caglioti; Károly Micskei; Claudia Zucchi; Gyula Pályi
Journal:  Orig Life Evol Biosph       Date:  2008-06-03       Impact factor: 1.950

2.  Multiple competing pathways for chemical reaction: drastic reaction shortcut for the self-catalytic double-helix formation of helicene oligomers.

Authors:  Yo Kushida; Nozomi Saito; Masanori Shigeno; Masahiko Yamaguchi
Journal:  Chem Sci       Date:  2016-10-14       Impact factor: 9.825

  2 in total

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