The particular nature of boron compounds allows an ample modularity of their properties ranging from Lewis acids, C-nucleophiles, B-nucleophiles, or even conjunctive reagents for new synthetic manipulations. Moreover, the increasing demand for functionalized boron derivatives for pharmaceutical or material science applications requires the development of new synthetic methods for boron introduction in organic compounds. This review summarizes the possible combinations of boron derivatives with a variety of strained heterocycles reported in the most recent literature. (Figure presented.).

Boron Reagents and Catalysts for the Functionalization of Strained Heterocycles

Pineschi M.
2021-01-01

Abstract

The particular nature of boron compounds allows an ample modularity of their properties ranging from Lewis acids, C-nucleophiles, B-nucleophiles, or even conjunctive reagents for new synthetic manipulations. Moreover, the increasing demand for functionalized boron derivatives for pharmaceutical or material science applications requires the development of new synthetic methods for boron introduction in organic compounds. This review summarizes the possible combinations of boron derivatives with a variety of strained heterocycles reported in the most recent literature. (Figure presented.).
2021
Pineschi, M.
File in questo prodotto:
File Dimensione Formato  
ASC accepted 2021.pdf

accesso aperto

Tipologia: Documento in Post-print
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 1.5 MB
Formato Adobe PDF
1.5 MB Adobe PDF Visualizza/Apri
ASC 2021.pdf

non disponibili

Tipologia: Documento in Post-print
Licenza: NON PUBBLICO - accesso privato/ristretto
Dimensione 2.44 MB
Formato Adobe PDF
2.44 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1100213
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 12
social impact