4.5 Article

Rhodium-Catalyzed [2+2+2] Cycloaddition-Aromatization of 1,6-Diynes with Cyclic Enol Ethers at Room Temperature

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2016, 期 1, 页码 132-138

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201501282

关键词

Homogeneous catalysis; Cycloaddition; Cyclization; Alkynes; Enol ethers; Rhodium

资金

  1. Japan Science and Technology Agency (ACT-C program)
  2. Japanese Ministry of Education, Culture, Sports, Science, and Technology (MEXT) [15H03775]
  3. Grants-in-Aid for Scientific Research [15J08332, 15H03775, 15H06201, 26102004] Funding Source: KAKEN

向作者/读者索取更多资源

A cationic rhodium(I)/BINAP [2,2-bis(diphenylphosphino)-1,1-binaphthyl] complex is capable of catalyzing the [2+2+2] cycloaddition-aromatization of 1,6-diynes with cyclic enol ethers (2,3-dihydrofuran and dihydropyran) at room temperature to produce the corresponding aryl alkanol derivatives in good yields. In this process, a conjugated dihydrofuran showed a significantly higher reactivity than a nonconjugated one.

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