4.5 Article

Lewis-Acid-Catalysed Tandem Meinwald Rearrangement/Intermolecular [3+2]-Cycloaddition of Epoxides with Donor-Acceptor Cyclopropanes: Synthesis of Functionalized Tetrahydrofurans

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2015, 期 11, 页码 2517-2523

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201403590

关键词

Asymmetric synthesis; Cyclization; Oxygen heterocycles; Small ring systems; Epoxides

资金

  1. Council of Scientific and Industrial Research (CSIR), New Delhi
  2. Indian Institute of Technology (IIT), Ropar
  3. Department of Science and Technology (DST), New Delhi [SR/FT/CS-84/2010]

向作者/读者索取更多资源

A Lewis-acid-catalysed tandem Meinwald rearrangement/[3+2]-cycloaddition of epoxides with donor-acceptor cyclopropanes to synthesize varieties of cis-2,5-aryl-benzyl-substituted tetrahydrofurans is described. An enantioselective version of the same transformation was achieved using an InCl3-PyBOX catalyst system.

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