Literature DB >> 33587741

Dialkynyldiboranes(4) and the selectable reactivity of their C-H, C[triple bond, length as m-dash]C and B-B bonds.

Fabian Schorr1, Felipe Fantuzzi2, Rian D Dewhurst1, Holger Braunschweig1.   

Abstract

The synthesis and reactivity of dialkynyldiboranes(4), a little-studied family of diboranes, are presented herein. Three dialkynyldiboranes(4) were prepared via two different salt metathesis pathways. The three reactive sites of these dialkynyldiboranes(4) are then selectively addressed by judicious application of reagents: addition of an amine N-oxide leads to oxygen insertion into the B-B bond, dicobaltoctacarbonyl binds to the alkynyl C[triple bond, length as m-dash]C bonds, while Sonogashira-Hagihara cross-coupling conditions lead to double C-C bond formation at the alkynyl C-H groups.

Entities:  

Year:  2021        PMID: 33587741     DOI: 10.1039/d1cc00265a

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


  1 in total

1.  Controlled Synthesis of Oligomers Containing Main-Chain B(sp2 )-B(sp2 ) Bonds.

Authors:  Fabian Schorr; Nils Schopper; Nicolas Riensch; Felipe Fantuzzi; Marco Neder; Rian D Dewhurst; Torsten Thiess; Tobias Brückner; Kai Hammond; Holger Helten; Maik Finze; Holger Braunschweig
Journal:  Chemistry       Date:  2021-10-11       Impact factor: 5.020

  1 in total

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