USE OF AZETIDINE SCAFFOLDS IN STEREOSELECTIVE TRANSFORMATIONS (MICROREVIEW)

Authors

  • Renzo Luisi Dipartimento di Farmacia-Scienze del Farmaco, University of Bari
  • Leonardo Degennaro Dipartimento di Farmacia-Scienze del Farmaco, University of Bari

DOI:

https://doi.org/10.1007/4483

Abstract

Noteworthy stereoselective approaches toward the synthesis of densely substituted azetidines are reported. This microreview covers a selection of the latest efficient methods for the functionalization of azetidine cores by metalation, C–H activation, radical or biocatalytic processes, as well as nonclassical and large-scale preparative procedures.

 

Author Biographies

Renzo Luisi, Dipartimento di Farmacia-Scienze del Farmaco, University of Bari

Department of Pharmacy - Drug Science University of Bari ITALY

Leonardo Degennaro, Dipartimento di Farmacia-Scienze del Farmaco, University of Bari

Department of Pharmacy - Drug Science University of Bari ITALY

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Published

2018-06-06

Issue

Vol. 54 No. 4 (2018): Stereoselective synthesis of heterocyclic compounds

Section

Heterocycles in Focus