Outside Back Cover: Straightforward Formation of Borirenes from Boroles and Dialkynes (Angew. Chem. 18/2025)

In their Research Article (e202423391), Felipe Fantuzzi, Eufrânio N. da Silva Júnior, Holger Braunschweig et al. report a selective one-step synthesis of perarylated borirenes from boroles and 1,3-diynes. The study includes substrate scope, X-ray, and DFT analyses. The cover illustrates this process with a phenyl balloon carrying a borirene ring arising above a sky filled with borole precursors, highlighting the novelty and aromaticity of the three-membered boron-bearing rings (Cover design: Danilo Londoño).

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Publication Details

Journal
Angewandte Chemie
Published
2025-03-30
DOI
https://doi.org/10.1002/ange.202506308
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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Outside Back Cover: Straightforward Formation of Borirenes from Boroles and Dialkynes (Angew. Chem. 18/2025)

Pedro Oliveira, Holger Braunschweig, Merle Arrowsmith, Marieli O. Rodrigues et al.
Angewandte Chemie
Organoboron and organosilicon chemistry
article

Outside Back Cover: Straightforward Formation of Borirenes from Boroles and Dialkynes (Angew. Chem. 18/2025)

Pedro Oliveira, Holger Braunschweig, Merle Arrowsmith, Marieli O. Rodrigues, Josina L. Bohlen, Eufrânio N. da Silva Júnior, Felipe Fantuzzi, Arumugam Jayaraman, Lukas Lubczyk, Caren D. G. da Silva
article en

Abstract

In their Research Article (e202423391), Felipe Fantuzzi, Eufrânio N. da Silva Júnior, Holger Braunschweig et al. report a selective one-step synthesis of perarylated borirenes from boroles and 1,3-diynes. The study includes substrate scope, X-ray, and DFT analyses. The cover illustrates this process with a phenyl balloon carrying a borirene ring arising above a sky filled with borole precursors, highlighting the novelty and aromaticity of the three-membered boron-bearing rings (Cover design: Danilo Londoño).

Angewandte ChemieVol. 137(18)
Universidade Federal de Minas Gerais (BR), University of Kent (GB), University of Würzburg (DE)
Openalex Percentile: Top 95%
Organoboron and organosilicon chemistry
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