Evidence map›Paper›PMID 39738011›Full record

ArticleNature communications2024

Asymmetric synthesis of atropisomers featuring cyclobutane boronic esters facilitated by ring-strained B-ate complexes.

Yu-Wen Sun, Jia-Hui Zhao, Xin-Yu Yan, Chong-Lei Ji, Huangdi Feng, De-Wei Gao

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  3. Review
  4. Review
  5. Article
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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

6 authors.

Yu-Wen Sun *School of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.ORCID http://orcid.org/0009-0003-9715-139X
Jia-Hui Zhao *College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China.ORCID http://orcid.org/0009-0002-9966-9873
Xin-Yu YanSchool of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Chong-Lei JiSchool of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China.ORCID http://orcid.org/0000-0001-7930-2324
Huangdi FengCollege of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China. hdfeng@sues.edu.cn.ORCID http://orcid.org/0000-0002-5500-8283
De-Wei GaoSchool of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210, China. gaodw@shanghaitech.edu.cn.ORCID http://orcid.org/0000-0002-6258-8378

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22101177National Natural Science Foundation of China (National Science Foundation of China) 22471166
6 · The paper itself

Abstract

The strain-release-driven reactions of bicyclo[1.1.0]butanes (BCBs) have received significant attention from chemists. Notably, 1,2-migratory reactions enabled by BCB-derived B-ate complexes effectively complement the reactions initiated by common BCBs. The desired products are particularly valuable for late-stage transformations due to the presence of the C-B bond. However, asymmetric reactions mediated by BCB-derived boronate complexes have progressed slowly. In this study, we develop an asymmetric synthesis of atropisomers featuring cis-cyclobutane boronic esters facilitated by 1,2-carbon or boron migration of ring-strained B-ate complexes, achieving high enantioselectivity. The reaction is compatible with various aryl, alkenyl, alkyl boronic esters and B

Identifiers

PMID39738011
PMCPMC11685450

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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.