Literature DB >> 19473047

Iron(II) triflate as an efficient catalyst for the imination of sulfoxides.

Olga García Mancheño1, Jonathan Dallimore, Andrew Plant, Carsten Bolm.   

Abstract

The challenging imination of benzyl-, sterically demanding alkyl-, and heteroaryl-substituted sulfoxides has been studied. Iron(II) triflate was identified as a highly efficient and robust catalyst for sulfur imination reactions. A variety of sulfoxides and sulfides were efficiently iminated with sulfonyliminoiodinanes (PhI=NSO(2)R) at room temperature to give the corresponding sulfoximines and sulfilimines in good yields and with short reaction times.

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Year:  2009        PMID: 19473047     DOI: 10.1021/ol900660x

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Enantioselective imidation of sulfides via enzyme-catalyzed intermolecular nitrogen-atom transfer.

Authors:  Christopher C Farwell; John A McIntosh; Todd K Hyster; Z Jane Wang; Frances H Arnold
Journal:  J Am Chem Soc       Date:  2014-06-05       Impact factor: 15.419

2.  Accessing Perfluoroaryl Sulfonimidamides and Sulfoximines via Photogenerated Perfluoroaryl Nitrenes: Synthesis and Application as a Chiral Auxiliary.

Authors:  Giampiero Proietti; Julius Kuzmin; Azamat Z Temerdashev; Peter Dinér
Journal:  J Org Chem       Date:  2021-11-12       Impact factor: 4.354

3.  Catalytic Enantioselective Synthesis of Pyridyl Sulfoximines.

Authors:  Yu Tang; Scott J Miller
Journal:  J Am Chem Soc       Date:  2021-06-14       Impact factor: 16.383

  3 in total

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