Literature DB >> 11971699

Cu(I)/bis(azaferrocene)-catalyzed enantioselective synthesis of beta-lactams via couplings of alkynes with nitrones.

Michael M-C Lo1, Gregory C Fu.   

Abstract

As a consequence of the wide-ranging significance of beta-lactams (e.g., use as drugs and as chiral building blocks), a great deal of effort has been dedicated to the development of methods for their stereoselective synthesis. Although considerable progress has been achieved, nearly all of the approaches that have been described are based on the use of chiral precursors; direct catalytic enantioselective routes to beta-lactams are rare as well as limited in scope. In this communication, we establish that, using a new C2-symmetric planar-chiral bis(azaferrocene) ligand, we can generate beta-lactams with very good enantiomeric excess and cis diastereoselection via catalytic enantioselective Kinugasa reactions (couplings of alkynes with nitrones). Appealing attributes of this process include the ready availability of the starting materials, the functional-group tolerance of the reaction, and the convergency of the approach.

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Year:  2002        PMID: 11971699     DOI: 10.1021/ja025833z

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


  8 in total

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5.  A highly stereoselective synthesis of chiral alpha-amino-beta-lactams via the Kinugasa reaction employing ynamides.

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7.  Reaction of an iron(IV) nitrido complex with cyclohexadienes: cycloaddition and hydrogen-atom abstraction.

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8.  Development of TsDPEN based imine-containing ligands for the copper-catalysed asymmetric Kinugasa reaction.

Authors:  Chuanlong Xu; Yuchen Yang; Yue Wu; Feilong He; Huakang He; Ping Deng; Hui Zhou
Journal:  RSC Adv       Date:  2020-05-12       Impact factor: 4.036

  8 in total

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