Neutral s<i>p</i><sup>2</sup>–s<i>p</i><sup>3</sup> Diboranes: Structures, Reactivities, and Applications in Organic Synthesis

Neutral s p 2 – s p 3 diboranes are characterized by a polarized BB single bond between two electronically and structurally distinct boryl groups, featuring one s p 2 ‐hybridized (three‐coordinate) boron center and one s p 3 ‐hybridized (four‐coordinate) boron center with a neutral Lewis base ligand. Their unique structures and properties have attracted growing research interest, particularly in exploring their reactivities and applications in CB bond formation reactions. This review summarizes recent advancements in the chemistry of neutral s p 2 –s p 3 diboranes, emphasizing their syntheses, structural features, reactivities, and emerging applications as diboron reagents in organic synthesis.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-04-29
DOI
https://doi.org/10.1002/ejoc.202500223
Citations
5
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
4.68

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article

Neutral sp2–sp3 Diboranes: Structures, Reactivities, and Applications in Organic Synthesis

Hairong Lyu, Zhiqing Liu
5 citations
European Journal of Organic Chemistry
Organoboron and organosilicon chemistry
4.68
article

Neutral sp2–sp3 Diboranes: Structures, Reactivities, and Applications in Organic Synthesis

Hairong Lyu, Zhiqing Liu
article en
5 citations

Abstract

Neutral s p 2 – s p 3 diboranes are characterized by a polarized BB single bond between two electronically and structurally distinct boryl groups, featuring one s p 2 ‐hybridized (three‐coordinate) boron center and one s p 3 ‐hybridized (four‐coordinate) boron center with a neutral Lewis base ligand. Their unique structures and properties have attracted growing research interest, particularly in exploring their reactivities and applications in CB bond formation reactions. This review summarizes recent advancements in the chemistry of neutral s p 2 –s p 3 diboranes, emphasizing their syntheses, structural features, reactivities, and emerging applications as diboron reagents in organic synthesis.

European Journal of Organic ChemistryVol. 28(23)
Chinese University of Hong Kong (HK), Southern University of Science and Technology (CN)
Croucher Foundation, National Natural Science Foundation of China, Chinese University of Hong Kong
Openalex Percentile: Top 6%
Organoboron and organosilicon chemistry
4.68
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