Literature DB >> 30124705

Transition-metal-free synthesis of vicinal triborated compounds and selective functionalisation of the internal C-B bond.

Elliot Davenport1, Elena Fernandez.   

Abstract

1,2,3-Triborated compounds can be prepared by simple nucleophilic borylation of 1,3-dienes, without the assistance of metal catalysts. Selective functionalisation of the internal C-B bond of the 1,2,3-triborated compounds, through cross-coupling with aryl iodides, highlights the powerful methodology toward polyfunctionalisation.

Entities:  

Year:  2018        PMID: 30124705     DOI: 10.1039/c8cc06153j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  1,2-Boron Shifts of β-Boryl Radicals Generated from Bis-boronic Esters Using Photoredox Catalysis.

Authors:  Daniel Kaiser; Adam Noble; Valerio Fasano; Varinder K Aggarwal
Journal:  J Am Chem Soc       Date:  2019-09-03       Impact factor: 15.419

2.  Selective Coupling of 1,2-Bis-Boronic Esters at the more Substituted Site through Visible-Light Activation of Electron Donor-Acceptor Complexes.

Authors:  Hui Wang; Jingjing Wu; Adam Noble; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-07       Impact factor: 16.823

Review 3.  Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents.

Authors:  Oriol Salvadó; Elena Fernández
Journal:  Molecules       Date:  2020-04-10       Impact factor: 4.411

  3 in total

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