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α-Amido sulphones as useful intermediates in the preparation of C-chiral α-aminophosphonates and α-aminophosphonic acids.
Gbubele, Joseph D; Misiaszek, Tomasz; Siczek, Milosz; Olszewski, Tomasz K.
Affiliation
  • Gbubele JD; Department of Physical and Quantum Chemistry, Faculty of Chemistry, Wroclaw University of Science and Technology, ul. Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland. tomasz.olszewski@pwr.edu.pl.
  • Misiaszek T; Department of Physical and Quantum Chemistry, Faculty of Chemistry, Wroclaw University of Science and Technology, ul. Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland. tomasz.olszewski@pwr.edu.pl.
  • Siczek M; Department of Chemistry, University of Wroclaw, F. Joliot-Curie 14, Wroclaw, Poland.
  • Olszewski TK; Department of Physical and Quantum Chemistry, Faculty of Chemistry, Wroclaw University of Science and Technology, ul. Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland. tomasz.olszewski@pwr.edu.pl.
Org Biomol Chem ; 21(30): 6180-6191, 2023 Aug 02.
Article in En | MEDLINE | ID: mdl-37466200
ABSTRACT
α-Amido sulphones have been used as useful starting materials in the preparation of C-chiral α-aminophosphonates and α-aminophosphonic acids. The developed methodology is based on a one-pot, base-catalysed in situ generation of an imine intermediate followed by addition of a phosphorus nucleophile. The presented protocol is simple and effective and can be applied to a variety of structurally diverse α-amido sulphones and phosphorus nucleophiles, leading to the desired pure products after simple crystallization in very good yields. Importantly, the use of H-phosphonate bearing a chiral auxiliary allows the reaction to be performed with high diastereoselectivity (a single diastereoisomer is generated and isolated) and the possibility of precise control of the configuration at the newly generated C-chiral centre.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2023 Document type: Article Affiliation country:
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