4.5 Article

Intramolecular enantioselective hydroamination catalyzed by rare earth binaphthylamides

期刊

JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 696, 期 1, 页码 255-262

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2010.09.013

关键词

Asymmetric intramolecular hydroamination; Carbon-nitrogen bond formation; Catalysis; Amines; Lanthanides; Pyrrolidines

资金

  1. CNRS
  2. MENSR
  3. ANR [07 367]
  4. Russian Foundation for Basic Research [08-03-92501]
  5. Russian Academy of Sciences

向作者/读者索取更多资源

Asymmetric intramolecular hydroamination reaction is a stately way to prepare chiral nitrogen-containing heterocyclic compounds. We report in this account our personal contribution in this field with the synthesis of chiral amido rare-earth complexes. A new family of structurally defined heterobimetallic rare earth lithium ate complexes based on N-substituted binaphthylamido ligands was discovered that promoted the hydroamination/cyclization of aminoolefins with up to 87% ee. Neutral rare earth amido and amido alkyl complexes could also be prepared and led to very active species. A more simple and reliable synthetic procedure was discovered towards the preparation of heterobimetallic rare earth amido alkyl ate complexes. They proved to be also active and enantioselective catalysts, as a good compromise between efficiency and practicability issues. (C) 2010 Elsevier B.V. All rights reserved.

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