Evidence map›Paper›PMID 30597884›Full record

ReviewMolecules (Basel, Switzerland)2018

Recent Synthesis Developments of Organoboron Compounds via Metal-Free Catalytic Borylation of Alkynes and Alkenes.

Yanmei Wen, Chunmei Deng, Jianying Xie, Xinhuang Kang

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Boron in Diet and Medicine: Mechanisms of Delivery and Detection.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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

4 authors.

Yanmei WenFaculty of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, China. wenym@gdou.edu.cn.
Chunmei DengFaculty of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, China. dcm2382405@163.com.
Jianying XieFaculty of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, China. xiejy1961@126.com.
Xinhuang KangFaculty of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, China. kang.xinhuang@aliyun.com.

Funding

Natural Science Foundation of Guangdong Province 2016A030313750Project of Enhancing School with Innovation of Guangdong Ocean University GDOU2017052502Zhanjiang Natural Science Foundation A14457Zhanjiang Natural Science Foundation A15445
6 · The paper itself

Abstract

Diboron reagents have been traditionally regarded as "Lewis acids", which can react with simple Lewis base to create a significant nucleophilic character in one of boryl moieties. In particular, bis(pinacolato)diboron (B₂pin₂) reacts with simple Lewis bases, such as

Indexed as

AlkenesAlkynesBoron CompoundsCatalysisHydrocarbonsMetalsAlkenesAlkynesBoron CompoundsHydrocarbonsMetalsalkenealkynemetal-free catalytic borationnucleophilic boronorganoboron compound

Identifiers

PMID30597884
PMCPMC6337501

What OpenQuestion holds

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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.