Literature DB >> 12375892

Simple synthesis of alpha-hydroxyamino carbonyl compounds: new scope of the nitroso aldol reaction.

Norie Momiyama1, Hisashi Yamamoto.   

Abstract

[reaction: see text] The reaction of nitroso compounds with enolates, "the nitroso aldol reaction", occurs in high yield to generate alpha-hydroxyamino carbonyl compounds. Yields range from 42% to 98% with N-selectivity >99:1 from commercially available aromatic or aliphatic nitroso compounds and a variety of alkali metal or tin enolates.

Entities:  

Year:  2002        PMID: 12375892     DOI: 10.1021/ol026443k

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


  5 in total

Review 1.  The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses.

Authors:  Brian S Bodnar; Marvin J Miller
Journal:  Angew Chem Int Ed Engl       Date:  2011-04-21       Impact factor: 15.336

2.  O-nitroso aldol synthesis: Catalytic enantioselective route to alpha-aminooxy carbonyl compounds via enamine intermediate.

Authors:  Norie Momiyama; Hiromi Torii; Susumu Saito; Hisashi Yamamoto
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-05       Impact factor: 11.205

3.  Regiochemical Reversals in Nitrosobenzene Reactions with Carbonyl Compounds: α-Aminooxyketone versus α-Hydroxyaminoketone Products.

Authors:  Donna J Nelson; Ravi Kumar
Journal:  European J Org Chem       Date:  2012-10

4.  A Lewis Acid Catalyzed annulation to 2,1-benzisoxazoles.

Authors:  Kate D Otley; Jonathan A Ellman
Journal:  J Org Chem       Date:  2014-08-26       Impact factor: 4.354

5.  Organocatalytic asymmetric nitroso aldol reaction of α-substituted malonamates.

Authors:  Ekta Gupta; Narendra Kumar Vaishanv; Sandeep Kumar; Raja Krishnan Purshottam; Ruchir Kant; Kishor Mohanan
Journal:  Beilstein J Org Chem       Date:  2022-02-21       Impact factor: 2.883

  5 in total

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