Novel Borylene Synthon: From Design, Synthesis to Application

Borylene (R–B:) is a concept derived from carbene, which refers to a carbon species with only six electrons in its valence shell. As a class of compounds extensively studied in main group chemistry, carbenes have long demonstrated broad applications in fields such as catalysis, synthesis, materials science, and pharmaceuticals. In contrast, borylenes—owing to their extremely high reactivity that is difficult to control—have yet to be widely applied in areas such as catalysis and synthesis. Even the free state of borylenes (R–B:) has not been isolated and stabilized. Notably, not only are carbon–boron bonds widely utilized for further functionalization, but numerous high-value pharmaceutical molecules also contain boron atoms. Therefore, employing borylenes as boron-inserting synthons, and even applying them to molecular skeleton editing via boron atom insertion, holds significant research value and application potential.

Authors

Institutions

Publication Details

Journal
California Digital Library
Published
2026-07-30
DOI
https://doi.org/10.48321/d16ec15539
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Novel Borylene Synthon: From Design, Synthesis to Application

Zhiqing Liu
California Digital Library
Organoboron and organosilicon chemistry
article

Novel Borylene Synthon: From Design, Synthesis to Application

Zhiqing Liu
article en

Abstract

Borylene (R–B:) is a concept derived from carbene, which refers to a carbon species with only six electrons in its valence shell. As a class of compounds extensively studied in main group chemistry, carbenes have long demonstrated broad applications in fields such as catalysis, synthesis, materials science, and pharmaceuticals. In contrast, borylenes—owing to their extremely high reactivity that is difficult to control—have yet to be widely applied in areas such as catalysis and synthesis. Even the free state of borylenes (R–B:) has not been isolated and stabilized. Notably, not only are carbon–boron bonds widely utilized for further functionalization, but numerous high-value pharmaceutical molecules also contain boron atoms. Therefore, employing borylenes as boron-inserting synthons, and even applying them to molecular skeleton editing via boron atom insertion, holds significant research value and application potential.

California Digital Library
Chinese University of Hong Kong (HK)
Openalex Percentile: Top 17%
Organoboron and organosilicon chemistry
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.