Evidence map›Paper›PMID 41778749›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2026

Synthesis of 1-Alkynylboronates, 1,1-Diborylalkenes, and 1,1,1-Triborylalkanes: Challenges and Opportunities.

Son Hoai Doan, Vu Nguyen Tran, Thanh Vinh Nguyen

Abstract readReview
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Son Hoai DoanSchool of Chemistry, University of New South Wales, Sydney, NSW, Australia.
Vu Nguyen TranSchool of Chemistry, University of New South Wales, Sydney, NSW, Australia.
Thanh Vinh NguyenSchool of Chemistry, University of New South Wales, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0002-0757-9970

Funding

Australian Research Council DP260100065
6 · The paper itself

Abstract

In the field of organoboron chemistry, multi(boronate) esters have emerged as crucial intermediates, with various applications in synthetic chemistry, material technology, and life sciences. This mini-review discusses recent advancement in the synthesis of these versatile compounds, particularly alkynylboronates, 1,1-diborylalkenes, and 1,1,1-triborylalkanes, all of which are derived from easily accessible alkenes and alkynes. The article provides an in-depth analysis of these methodologies, delves into their mechanistic underpinnings, and emphasises their synthetic utility. Future research avenues and unresolved challenges in organoboron chemistry are also identified in this report, aiming to inspire further development of synthetic methods used in this area.

Indexed as

coupling reactionfunctionalizationmixed borationmultiborationorganoboron

Identifiers

PMID41778749
PMCPMC13206542

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.