Related Experiment Video
Updated: Jan 10, 2026

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
Conceptual Expansion of Virtual Ligand Strategy Toward the Design of Triarylborane Catalysts
Ken Hirose1, Satoshi Maeda2,3,4, Wataru Matsuoka2,3,4
1Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.
Abstract:
Triarylboranes are among the most important classes of Lewis acid catalysts. However, the molecular design of triarylborane still relies on conventional trial-and-error strategies. This study introduces the virtual borane (VB) method, an original computational approach for the design of triarylborane based on the previously reported virtual ligand strategy. Using quantum chemical calculations, the VB reproduces the electronic and steric properties of various triarylboranes without explicitly requiring knowledge of their molecular structures. This, in turn, enables the rapid parameter-based optimization of the catalyst properties, affording rational and quantitative guidelines for molecular design. The accuracy of the VB method was validated by reproducing the energy diagrams of borane-catalyzed reactions. The utility of this method was demonstrated by virtual borane-assisted optimization, in which the optimal properties for transfer hydrosilylation were rapidly determined by numerical optimization of the VB parameters. The VBAO calculations were used to predict a superior catalyst, which was computationally validated.
More Related Videos
04:51Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
Published on: June 23, 2023
19:58Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Related Concept Videos
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Hydroboration-Oxidation of Alkenes
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Hybridization of Atomic Orbitals I
Valence Bond Theory
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene