Literature DB >> 15355085

Catalytic enantioselective Michael addition of 1,3-dicarbonyl compounds to nitroalkenes catalyzed by well-defined chiral ru amido complexes.

Masahito Watanabe1, Ayako Ikagawa, Hui Wang, Kunihiko Murata, Takao Ikariya.   

Abstract

Well-defined chiral Ru amido complexes promoted asymmetric Michael addition of 1,3-dicarbonyl compounds including malonates, beta-keto esters, and 1,3-diketones to nitroalkenes to give the corresponding adducts with excellent ees and in excellent yields.

Entities:  

Year:  2004        PMID： 15355085     DOI： 10.1021/ja046296g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  4 in total

1.  Synthesis of Ruthenium Boryl Analogues of the Shvo Metal-Ligand Bifunctional Catalyst.

Authors:  Liza Koren-Selfridge; Ian P Query; Joel A Hanson; Nicholas A Isley; Ilia A Guzei; Timothy B Clark
Journal:  Organometallics       Date:  2010       Impact factor: 3.876

2.  Direct asymmetric Michael addition to nitroalkenes: vinylogous nucleophilicity under dinuclear zinc catalysis.

Authors:  Barry M Trost; Julien Hitce
Journal:  J Am Chem Soc       Date:  2009-04-08       Impact factor: 15.419

3.  Catalytic asymmetric 1,4-additions of beta-keto esters to nitroalkenes promoted by a bifunctional homobimetallic Co2-Schiff base complex.

Authors:  Makoto Furutachi; Zhihua Chen; Shigeki Matsunaga; Masakatsu Shibasaki
Journal:  Molecules       Date:  2010-01-22       Impact factor: 4.411

4.  Exploiting the Chiral Ligands of Bis(imidazolinyl)- and Bis(oxazolinyl)thiophenes-Synthesis and Application in Cu-Catalyzed Friedel-Crafts Asymmetric Alkylation.

Authors:  Mohammad Shahidul Islam; Abdullah Saleh Alammari; Assem Barakat; Saeed Alshahrani; Matti Haukka; Abdullah Mohammed Al-Majid
Journal:  Molecules       Date:  2021-12-06       Impact factor: 4.411
  4 in total

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