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Regio- and Stereoselective Synthesis of Sulfur-Bearing Four-Membered Heterocycles: Direct Access to 2,4-Disubstituted Thietane 1-Oxides.
Degennaro, Leonardo; Carroccia, Laura; Parisi, Giovanna; Zenzola, Marina; Romanazzi, Giuseppe; Fanelli, Flavio; Pisano, Luisa; Luisi, Renzo.
Affiliation
  • Degennaro L; Department of Pharmacy - Drug Sciences, University of Bari "A. Moro" , Via E. Orabona 4, 70125 Bari, Italy.
  • Carroccia L; Department of Pharmacy - Drug Sciences, University of Bari "A. Moro" , Via E. Orabona 4, 70125 Bari, Italy.
  • Parisi G; Department of Pharmacy - Drug Sciences, University of Bari "A. Moro" , Via E. Orabona 4, 70125 Bari, Italy.
  • Zenzola M; Department of Pharmacy - Drug Sciences, University of Bari "A. Moro" , Via E. Orabona 4, 70125 Bari, Italy.
  • Romanazzi G; DICATECh, Politecnico di Bari , Via Orabona 4, 70125 Bari, Italy.
  • Fanelli F; CNR NANOTEC-Istituto di Nanotecnologia , Polo di Nanotecnologia c/o Campus Ecotekne, via Monteroni, 73100 Lecce, Italy.
  • Pisano L; Department of Pharmacy - Drug Sciences, University of Bari "A. Moro" , Via E. Orabona 4, 70125 Bari, Italy.
  • Luisi R; CNR, Institute of Crystallography IC-CNR , Amendola, 122/o, 70125 Bari, Italy.
J Org Chem ; 80(24): 12201-11, 2015 Dec 18.
Article in En | MEDLINE | ID: mdl-26566011
ABSTRACT
Starting from readily available C2-substituted thietane 1-oxides, a straightforward synthesis of new C2,C4-disubstituted thietane 1-oxides has been developed by using a lithiation/electrophilic trapping sequence. The chemical and configurational stability of lithiated C2-substituted thietane 1-oxides has been investigated as well as the stereochemical implications for this process. The results demonstrate that a stereoselective functionalization at the C2, C4 positions of a thietane is feasible, leaving intact the four-membered ring.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Org Chem Year: 2015 Document type: Article Affiliation country: Italia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Org Chem Year: 2015 Document type: Article Affiliation country: Italia
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