Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Yongzheng Ding"'
Publikováno v:
Journal of the American Chemical Society; 7/24/2024, Vol. 146 Issue 29, p19635-19642, 8p
Publikováno v:
The Journal of Organic Chemistry. 88:5194-5204
Autor:
Yongzheng Ding, Hanmin Huang
Publikováno v:
Chem Catalysis. 2:1467-1479
Autor:
Puran Singh Sijwali, Yongzheng Ding, Chunhua Ma, Vijaykumar Pillalamarri, Priyanka Sankoju, Yingjie Zhang, Bharati Reddi, Anil Kumar Marapaka, Guozhen Zhang, Anthony Addlagatta, Renu Sudhakar
Publikováno v:
Chinese Chemical Letters. 33:2550-2554
Plasmodium parasites causing malaria have developed resistance to most of the antimalarials in use, including the artemisinin-based combinations, which are the last line of defense against malaria. This necessitates the discovery of new targets and t
Publikováno v:
Organic Chemistry Frontiers. 9:715-719
A palladium-catalyzed intermolecular and intramolecular hydrocarbonylative cycloaddition to access bridged lactones was reported.
Publikováno v:
Organic & Biomolecular Chemistry. 20:3917-3921
A palladium-catalyzed carbonylative lactonization reaction of 2-halidearomatic aldehydes and CO with H2O as a nucleophile is described, which provides a strategy for the synthesis of diversely substituted 3,3′-oxyphthalides and phthalides.
Autor:
Hui Yu, Yongzheng Ding, Jinglai Sun, Xuyao Yu, Fengling Zhu, Huanming Li, Xiaoyun Liang, Dagong Jia
Publikováno v:
Proceedings of the 2022 9th International Conference on Biomedical and Bioinformatics Engineering.
Publikováno v:
Organic letters. 24(43)
A catalytic system combined with NiBr
Publikováno v:
Chemistry – An Asian Journal. 15:1678-1682
Supporting information for this article is given via a link at the end of the document. By intercepting the acylpalladium species with C=N bond of azaarenes or imines other than free amines or alcohols, the difunctionalization of C=N bond was establi
Publikováno v:
Chemical Communications. 56:12198-12201
A novel palladium-catalyzed highly selective hydrocarbonylative cycloaddition reaction with two different alkenes in the presence of CO enabled by a reactive directing-group is developed, which offers efficient and convenient access to lactone-contai