Literature DB >> 24552183

Practical approach for asymmetric hydroxyamination of aldehydes with in situ generated nitrosocarbonyl compounds: application to one-pot synthesis of chiral allylamines.

Taichi Kano1, Fumitaka Shirozu, Keiji Maruoka.   

Abstract

The highly regio- and enantioselective hydroxyamination of aldehydes with in situ generated nitrosocarbonyl compounds from a hydroxamic acid derivative was realized by simple and readily available chiral amine catalysts. The resulting hydroxyamination products were readily converted to the corresponding chiral 1,2-aminoalcohol or allylamine derivatives in one pot.

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Year:  2014        PMID: 24552183     DOI: 10.1021/ol5000742

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


  2 in total

1.  A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones.

Authors:  Dillon H Miles; Joan Guasch; F Dean Toste
Journal:  J Am Chem Soc       Date:  2015-06-12       Impact factor: 15.419

2.  Iron complexes of tetramine ligands catalyse allylic hydroxyamination via a nitroso-ene mechanism.

Authors:  David Porter; Belinda M-L Poon; Peter J Rutledge
Journal:  Beilstein J Org Chem       Date:  2015-12-11       Impact factor: 2.883

  2 in total

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