4.6 Article

Acid-catalyzed tandem reaction for the synthesis of pyridine derivatives via C=C/C(sp3)-N bond cleavage of enones and primary amines

期刊

RSC ADVANCES
卷 7, 期 22, 页码 13123-13129

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ra00780a

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资金

  1. National Natural Science Foundation of China [21362002, 81260472]
  2. Guangxi Natural Science Foundation of China [2014GXNSFDA118007, 2016GXNSFEA380001]
  3. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2014-A02, CMEMR2012-A20]
  4. Fund of Guangxi Key Laboratory of Functional Phytochemicals Research and Utilization [FPRU2015-2]
  5. Guangxi's Medicine Talented Persons Small Highland Foundation [1306]

向作者/读者索取更多资源

A one-pot acid-catalyzed tandem reaction has been developed without any metallic reagents or extra oxidants. This reaction involves a C=C bond cleavage of enones via a masked reverse Aldol reaction, and C(sp(3))-N bond cleavage of primary amines to provide nitrogen sources for the assembly of pyridine derivatives in high yields with excellent functional group tolerance.

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