One-pot construction of functionalized aziridines and maleimides via a novel pseudo-Knoevenagel cascade reaction.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
18 Feb 2020
Historique:
pubmed: 24 1 2020
medline: 29 2 2020
entrez: 24 1 2020
Statut: ppublish

Résumé

An Ugi, novel pseudo-Knoevenagel, ring expansion cascade reaction was discovered and utilized for the synthesis of aziridinyl succinimides in one-pot. Subsequently, densely functionalized aziridines and maleimides have been designed and synthesized through similar cascade reactions. The target compounds were prepared by means of a mild reaction and a simple operation procedure, which could be applicable to a broad scope of starting materials. This series of novel cascade reactions generates opportunities for the tailored synthesis of a wide range of biologically active scaffolds through tuneable Ugi inputs. Discovery of compound 8i with comparable potency to sorafenib in liver cancer cell lines could provide a new avenue for liver cancer drug discovery.

Identifiants

pubmed: 31971170
doi: 10.1039/c9cc08220d
doi:

Substances chimiques

Antineoplastic Agents 0
Aziridines 0
Maleimides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2194-2197

Commentaires et corrections

Type : ErratumIn

Auteurs

Jie Lei (J)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn and Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. HLi2@uams.edu.

Gui-Ting Song (GT)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

Liu-Jun He (LJ)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

Ya-Fei Luo (YF)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

Dian-Yong Tang (DY)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

Hui-Kuan Lin (HK)

Department of Cancer Biology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina 27157, USA.

Brendan Frett (B)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. HLi2@uams.edu.

Hong-Yu Li (HY)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. HLi2@uams.edu.

Zhong-Zhu Chen (ZZ)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

Zhi-Gang Xu (ZG)

College of Pharmacy, Chongqing University of Arts and Sciences, 319 Honghe Ave., Yongchuan, Chongqing, 402160, China. 18883138277@163.com xzg@cqwu.edu.cn.

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Classifications MeSH