Evidence map›Paper›PMID 36697919›Full record

ArticleCommunications chemistry2022

Manipulations of phenylnorbornyl palladium species for multicomponent construction of a bridged polycyclic privileged scaffold.

Lina Yin, Ting Guan, Jie Cheng, Dongchao Pan, Jinyang Lu, Jiahui Huang, Jiaqi Wu, Xiaoli Chen, Taiyun You, Xuting Huo and 3 more

Abstract read
In one paragraph

Article in Communications chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A Unified Approach for the Synthesis of Conformationally Locked and spChemistry (Weinheim an der Bergstrasse, Germany) · 2026
    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

13 authors.

Lina YinSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China. linayin@gzucm.edu.cn.ORCID http://orcid.org/0000-0002-6734-521X
Ting Guan *School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Jie Cheng *School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Dongchao Pan *School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Jinyang Lu *School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Jiahui HuangSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Jiaqi WuSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Xiaoli ChenSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Taiyun YouSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Xuting HuoSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Yuting HeSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China.
Jiayun PangSchool of Science, Faculty of Engineering and Science, University of Greenwich Medway Campus, Central Avenue, Chatham Maritime, Chatham, ME4 3RL, UK. j.pang@gre.ac.uk.ORCID http://orcid.org/0000-0003-0689-8440
Qingzhong HuSchool of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, Panyu, 510006, Guangzhou, People's Republic of China. huqqzh@gzucm.edu.cn.ORCID http://orcid.org/0000-0002-8880-4948

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81872739
6 · The paper itself

Abstract

Hexahydromethanocarbazole is a privileged scaffold in the discovery of new drugs and photoactive organic materials due to its good balance between structural complexity and minimized entropy penalty upon receptor binding. To address the difficulty of synthesizing this highly desirable bridged polycyclic scaffold, we designed a convenient multicomponent reaction cascade as intercepted Heck addition/C-H activation/C-palladacycle formation/electrophilic attack of ANP/N-palladacycle formation/Buchwald amination. A distinguishing feature of this sophisticated strategy is the successive generation of two key phenylnorbornyl palladium species to control the reaction flow towards desired products. DFT calculations further reveal the crucial roles of Cs

Identifiers

PMID36697919
PMCPMC9814782

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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.