Literature DB >> 18386903

Asymmetric nitroaldol reaction catalyzed by a C2-symmetric bisoxazolidine ligand.

Shuanglong Liu1, Christian Wolf.   

Abstract

A C2-symmetric bisoxazolidine was found to effectively catalyze the asymmetric Henry reaction of aliphatic and aromatic aldehydes. Beta-hydroxy nitroalkanes were produced in up to 99% yield and 95% ee. The bisoxazolidine-catalyzed nitroaldol formation requires relatively short reaction times, proceeds under mild conditions and is applicable to a wide range of substrates including sterically hindered aldehydes.

Entities:  

Year:  2008        PMID: 18386903     DOI: 10.1021/ol800442s

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


  2 in total

1.  Catalytic Enantioselective Ynamide Additions to Isatins: Concise Access to Oxindole Alkaloids.

Authors:  Max Moskowitz; Christian Wolf
Journal:  Angew Chem Int Ed Engl       Date:  2019-02-14       Impact factor: 15.336

2.  Organocatalytic Insertion of Isatins into Aryl Difluoronitromethyl Ketones.

Authors:  Ransheng Ding; Pegah R Bakhshi; Christian Wolf
Journal:  J Org Chem       Date:  2017-01-09       Impact factor: 4.354

  2 in total

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