Literature DB >> 15058921

Application of P,N-sulfinyl imine ligands to iridium-catalyzed asymmetric hydrogenation of olefins.

Laurie B Schenkel1, Jonathan A Ellman.   

Abstract

The utility of a novel class of P,N-ligands incorporating a chiral sulfinyl imine moiety is demonstrated in the iridium-catalyzed hydrogenation of both functionalized and unfunctionalized olefins, in which enantioselectivities of up to 94% are achieved. The modularity of the P,N-sulfinyl ligand class is highlighted by the facile preparation of a variety of sterically and electronically different ligands. Interesting structure-activity data for both the phosphine and sulfinamide components is provided by this expanded ligand set.

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Year:  2004        PMID: 15058921     DOI: 10.1021/jo035675+

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  The tert-butylsulfinamide lynchpin in transition-metal-mediated multiscaffold library synthesis.

Authors:  Renato A Bauer; Christine M DiBlasi; Derek S Tan
Journal:  Org Lett       Date:  2010-05-07       Impact factor: 6.005

2.  Modern Stereoselective Synthesis of Chiral Sulfinyl Compounds.

Authors:  Elżbieta Wojaczyńska; Jacek Wojaczyński
Journal:  Chem Rev       Date:  2020-04-29       Impact factor: 60.622

  2 in total

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