Literature DB >> 29711463

Enantioselective Ring Opening of Epoxides with 4-Methoxyphenol Catalyzed by Gallium Heterobimetallic Complexes: An Efficient Method for the Synthesis of Optically Active 1,2-Diol Monoethers.

Takehiko Iida1, Noriyoshi Yamamoto1, Shigeki Matsunaga1, Hee-Gweon Woo2, Masakatsu Shibasaki1.   

Abstract

Useful chiral building blocks such as 1,2-diols can be obtained by the enantioselective ring opening of achiral epoxides with oxygen nucleophiles. The ring opening is carried out effectively (up to 94 % ee) with 4-methoxyphenol and catalytic amounts of gallium complexes. The novel complex GaSO 1 displays a particularly high catalytic activity. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  Asymmetric catalysis; Asymmetric synthesis; Epoxides; Gallium; Oxygen nucleophiles

Year:  1998        PMID: 29711463     DOI: 10.1002/(SICI)1521-3773(19980904)37:16<2223::AID-ANIE2223>3.0.CO;2-Z

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  A new method for the synthesis of H(4)-BINOL.

Authors:  Lars V Heumann; Gary E Keck
Journal:  J Org Chem       Date:  2008-05-20       Impact factor: 4.354

  1 in total

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