ArticleRSC advances2023
Collective synthesis of aspulvinone and its analogues by vinylogous aldol condensation of substituted tetronic acids with aldehydes.
Xiaotan Yu, Xiaoxia Gu, Yunpeng Zhao, Fengqing Wang, Weiguang Sun, Changxing Qi, Lianghu Gu, Yonghui Zhang
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In one paragraphArticle in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Xiaotan YuHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.ORCID https://orcid.org/0000-0002-4029-810X Xiaoxia GuHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Yunpeng ZhaoHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Fengqing WangHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Weiguang SunHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Changxing QiHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Lianghu GuHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.
Yonghui ZhangHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030 People's Republic of China zhangyh@mails.tjmu.edu.cn gulianghu@hust.edu.cn qichangxing@hust.edu.cn.ORCID https://orcid.org/0000-0002-7222-2142 Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
A mild, modular and efficient synthetic method with broad substrate scope was developed for aspulvinones. Nine natural aspulvinones were synthesized, six of which were for the first time. The aldol condensation delivered
Identifiers
PMID36760298
PMCPMC9903353
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