Cover Feature: (ChemCatChem 18/2024)

The Cover Feature represents the key intermediate in the hydroboration of a ketone promoted by a novel complex. The diiron scaffold together with the amino pendant of the hydrocarbyl ligand plays an important role in this process, with main interactions depicted as beam of lights, connecting the interacting moieties. In their Research Article, Marcello Crucianelli and co-workers present the synthesis of new diiron organometallic complexes bearing functionalities with different electronic and steric properties. A wide screening study of these molecules allowed to evaluate their catalytic activity in the hydroboration with pinacolborane, efficiently converting carbonyl compounds into organoboronates, under mild conditions. More information can be found in the Research Article by F. Marchetti, A. Di Giuseppe, M. Crucianelli, and co-workers (DOI: 10.1002/cctc.202400811).

Authors

Publication Details

Journal
ChemCatChem
Published
2024-09-23
DOI
https://doi.org/10.1002/cctc.202481802
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Cover Feature: (ChemCatChem 18/2024)

Stefano Zacchini, Chiara Zappelli, Andrea Di Giuseppe, Francesco Taglieri et al.
ChemCatChem
Organoboron and organosilicon chemistry
article

Cover Feature: (ChemCatChem 18/2024)

Stefano Zacchini, Chiara Zappelli, Andrea Di Giuseppe, Francesco Taglieri, Tiziana Funaioli, Fabio Marchetti, Marcello Crucianelli, Silvia Schoch, Giulio Bresciani
article en

Abstract

The Cover Feature represents the key intermediate in the hydroboration of a ketone promoted by a novel complex. The diiron scaffold together with the amino pendant of the hydrocarbyl ligand plays an important role in this process, with main interactions depicted as beam of lights, connecting the interacting moieties. In their Research Article, Marcello Crucianelli and co-workers present the synthesis of new diiron organometallic complexes bearing functionalities with different electronic and steric properties. A wide screening study of these molecules allowed to evaluate their catalytic activity in the hydroboration with pinacolborane, efficiently converting carbonyl compounds into organoboronates, under mild conditions. More information can be found in the Research Article by F. Marchetti, A. Di Giuseppe, M. Crucianelli, and co-workers (DOI: 10.1002/cctc.202400811).

ChemCatChemVol. 16(18)
Openalex Percentile: Top 82%
Organoboron and organosilicon chemistry
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