Evidence map›Paper›PMID 41224794›Full record

ArticleNature communications2025

Catalytic asymmetric constructions of nitrogen, boron and carbon continuous stereogenic centers.

Guan Zhang, Junyi Jia, Xuzhao Du, Bofan Feng, Kai Yang, Peiyuan Yu, Qiuling Song

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. 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

7 authors.

Guan ZhangCollege of Chemistry and Materials Science, Fujian Normal University, Fuzhou, Fujian, China.
Junyi JiaKey Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry at Fuzhou University, Fuzhou, Fujian, China.
Xuzhao DuDepartment of Chemistry and Shenzhen Grubbs Institute, Southern University of Science and Technology Shenzhen, Guangdong, China.
Bofan FengKey Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry at Fuzhou University, Fuzhou, Fujian, China.
Kai YangKey Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry at Fuzhou University, Fuzhou, Fujian, China.ORCID http://orcid.org/0000-0002-1495-5380
Peiyuan YuDepartment of Chemistry and Shenzhen Grubbs Institute, Southern University of Science and Technology Shenzhen, Guangdong, China.ORCID http://orcid.org/0000-0002-4367-6866
Qiuling SongKey Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry at Fuzhou University, Fuzhou, Fujian, China. qsong@fzu.edu.cn.ORCID http://orcid.org/0000-0002-9836-8860

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22271105, 21931013Natural Science Foundation of Fujian Province (Fujian Provincial Natural Science Foundation) 2022J05016
6 · The paper itself

Abstract

Precise construction of molecular chirality is a longstanding scientific challenge in synthetic chemistry. Although methods to enantioselectively assemble consecutive carbon stereocenters are abundant, courses to establish enriched continuous heteroatomic stereocenters have acquired less attention and remain a tremendous challenge. Of those atoms in main group elements, nitrogen and boron are the most intractable ones to control their chirality. The copper-catalyzed asymmetric insertion reaction is one of the most significant transformations to construct C-B bonds in organic synthesis. Herein, we report a protocol to synthesize troublesome continuous heteroatomic stereocenters from cyclic amine boranes and diazo compounds via asymmetric B-H insertion reaction. The protocol is compatible with a wide range of amine boranes and diazo compounds, exhibiting high diastereo- and enantioselectivities. Mechanistic studies reveal a meaningful kinetic resolution pathway involved in the transformation and DFT calculations elucidate the origins of stereoselectivity and diastereoselectivity.

Identifiers

PMID41224794
PMCPMC12612116

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