Evidence map›Paper›PMID 40630678›Full record

ArticleRSC advances2025

Unified approach to synthesize diverse heterocyclics: a metal-free visible-light-promoted cyclization reaction to acquire sulfonylated spiro-trienones, coumarins and their derivatives.

Xin Sun, Si-Yu Li, Su-Yue Chen, Cheng-Cheng Zhang, Jia Li, Bin Zhang, Xiang-Fei Zhang, Jianghong Dong, Wen-Ke Bai, Xin-Qi Hao and 3 more

Abstract read
In one paragraph

Article in RSC advances, 2025. 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

13 authors.

Xin SunSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.ORCID https://orcid.org/0000-0001-7941-7113
Si-Yu LiSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Su-Yue ChenSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Cheng-Cheng ZhangSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Jia LiSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Bin ZhangSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Xiang-Fei ZhangSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Jianghong DongSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.ORCID https://orcid.org/0000-0002-3008-3594
Wen-Ke BaiHenan Wei Nuo Biotechnology Co., Ltd Zhumadian 463000 China.
Xin-Qi HaoGreen Catalysis Center and College of Chemistry, Zhengzhou University Zhengzhou 450001 China.ORCID https://orcid.org/0000-0003-1942-8309
Qi-Jie XuSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.
Bin WuSchool of Pharmaceutical Sciences, South-Central Minzu University Wuhan 430074 China 2015084@mail.scuec.edu.cn.ORCID https://orcid.org/0000-0001-6048-4965
Miao YuSchool of Chemistry and Pharmaceutical Engineering, Huanghuai University Zhumadian 463000 China sunxin@bjmu.edu.cn miaoy050666@126.com qijie001@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, a visible-light-promoted 9-thioxanthone-catalyzed cascade cyclization reaction to synthesize sulfonylated spiro-trienones, coumarins and their derivatives in yields of up to 98% under mild irradiation reaction conditions is reported. Furthermore, extensive studies, including gram-scale, radical capture, isotope and DFT experiments, were performed to gain insights into the possible reaction mechanism.

Identifiers

PMID40630678
PMCPMC12235599

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Registered trials

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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.