Enantioselective sulfonylation to construct 3-sulfonylated oxindoles

Article Properties
  • Language
    English
  • DOI (url)
  • Publication Date
    2024/01/01
  • Indian UGC (journal)
  • Refrences
    39
  • Hongye Li Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China
  • Yuqiao Zhou Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China ORCID (unauthenticated)
  • Zheng Tan Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China
  • Xiangyu Wang Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China
  • Yuxin Zhang Center for Natural Products Research, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610064, China
  • Fei Wang Center for Natural Products Research, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610064, China
  • Xiaoming Feng Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China ORCID (unauthenticated)
  • Xiaohua Liu Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China ORCID (unauthenticated)
Abstract
Cite
Li, Hongye, et al. “Enantioselective Sulfonylation to Construct 3-Sulfonylated Oxindoles”. Chemical Communications, vol. 60, no. 32, 2024, pp. 4354-7, https://doi.org/10.1039/d4cc00802b.
Li, H., Zhou, Y., Tan, Z., Wang, X., Zhang, Y., Wang, F., Feng, X., & Liu, X. (2024). Enantioselective sulfonylation to construct 3-sulfonylated oxindoles. Chemical Communications, 60(32), 4354-4357. https://doi.org/10.1039/d4cc00802b
Li, Hongye, Yuqiao Zhou, Zheng Tan, Xiangyu Wang, Yuxin Zhang, Fei Wang, Xiaoming Feng, and Xiaohua Liu. “Enantioselective Sulfonylation to Construct 3-Sulfonylated Oxindoles”. Chemical Communications 60, no. 32 (2024): 4354-57. https://doi.org/10.1039/d4cc00802b.
Li H, Zhou Y, Tan Z, Wang X, Zhang Y, Wang F, et al. Enantioselective sulfonylation to construct 3-sulfonylated oxindoles. Chemical Communications. 2024;60(32):4354-7.
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10.1039/D3RA03800A RSC Advances
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10.1039/D3QO00566F Organic Chemistry Frontiers
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry
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Refrences Analysis
The category Science: Chemistry 26 is the most frequently represented among the references in this article. It primarily includes studies from Organic Letters and Accounts of Chemical Research. The chart below illustrates the number of referenced publications per year.
Refrences used by this article by year