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Reduction reactions are among the most commonly employed methods in organic synthesis, both in the laboratory and industry. Typical reductants include hydrogen gas, as well as metal-, silicon-, and boron-based hydrides. Although hydrogen gas is considered the greenest reductant, its production currently depends heavily on fossil fuel-derived processes. Metal-, silicon-, and boron-hydrides are effective but often inconvenient to handle, and their preparation is energy-intensive. In recent decades, the use of diboron compounds as reductants has gained increasing attention. These compounds can generate hydrogen gas from protic solvents effectively for hydrogenation reactions and can also be used for hydrofunctionalization and deoxygenation transformations. This review highlights various types of diboron compounds, elucidates their mechanisms in these transformations, and discusses representative examples from recent literature.
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http://dx.doi.org/10.1039/d5cc03873a | DOI Listing |
Chem Sci
August 2025
Centro de Química Teórica & Computacional (CQT&C), Facultad de Ciencias Exactas, Departamento de Ciencias Químicas, Universidad Andrés Bello Avenida República 275 8370146 Santiago de Chile Chile
Clusters composed of heavy elements, particularly actinides, provide a compelling platform for exploring unconventional bonding and the role of relativistic effects in electronic structure and stability. In this study, we critically reassess the -symmetric PaB cluster, previously claimed to exhibit double Möbius-Craig aromaticity through delocalization of 4σ and 4π electrons. Our potential energy surface (PES) analysis disproves this assignment by showing that the structure is a higher-energy isomer; the most stable form adopts a distorted tetrahedral structure.
View Article and Find Full Text PDFOrg Lett
September 2025
State Key Laboratory of Drug Research, Shanghai Institute of MateriaMedica, Chinese Academy of Sciences, Shanghai 201203, P. R. China.
DNA-encoded chemical library (DECL) technology has emerged as a pivotal platform for high-throughput screening in drug discovery. Expanding the chemical space of DECLs requires the development of novel, robust, and DNA-compatible transformations, with atom-economical cyclizations being particularly attractive for generating drug-like scaffolds. The 7,8-dihydropteridinone core represents a pharmacologically important heterocycle whose incorporation into DECLs has been hampered by harsh synthetic conditions.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Department of Applied Chemistry, School of Engineering, The University of Tokyo, 4-6-1, Komaba, Meguro-ku, Tokyo 153-8505, Japan.
The first structurally characterized -(silyl)(boryl)nickel complex was synthesized the oxidative addition of a silylborane with a nickel(0) center, which represents a less studied process than the equivalent reactions with disilane and diboron compounds. The reactivity of the (silyl)(boryl)nickel complex with organic unsaturated molecules is also presented.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Department of Chemistry, College of Science, China Agricultural University, 2 Yuanmingyuan West Road, Beijing 100193, P. R. China.
Reduction reactions are among the most commonly employed methods in organic synthesis, both in the laboratory and industry. Typical reductants include hydrogen gas, as well as metal-, silicon-, and boron-based hydrides. Although hydrogen gas is considered the greenest reductant, its production currently depends heavily on fossil fuel-derived processes.
View Article and Find Full Text PDFNat Commun
July 2025
Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong SAR, PR China.
Borylation chemistry plays a crucial role in the development of new synthetic methodologies. However, the reactivity of zinc-boryl species has not been fully explored, particularly in relation to diverse reaction pathways. Here we show that a zinc-boryl species is successfully synthesized from bis(catecholato)diboron, exhibiting amphiphilic reactivity.
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