Autor: |
Nalivela, Kumara Swamy, Rudolph, Matthias, Baeissa, Elham S., Alhogbi, Basma G., Mkhalid, Ibraheem A. I., Hashmi, A. Stephen K. |
Předmět: |
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Zdroj: |
Advanced Synthesis & Catalysis; 6/5/2018, Vol. 360 Issue 11, p2183-2190, 8p |
Abstrakt: |
Abstract: A convenient protocol for the enantioselective synthesis of oxazole α‐hydroxy ester derivatives 4 from readily available propargylamides 1 and alkylglyoxylates 3 was developed. The first step of the one‐pot procedure is the selective intramolecular in situ formation of an alkylideneoxazoline 2, which then in an intermolecular reaction is enantioselectively transformed to the oxazole α‐hydroxy ester derivatives 4 in quantitative yield and good to excellent enantioselectivity via an asymmetric copper(II)‐catalyzed Alder‐ene reaction. [ABSTRACT FROM AUTHOR] |
Databáze: |
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