Literature DB >> 19226588

Catalytic asymmetric cycloaddition of ketenes and nitroso compounds: enantioselective synthesis of alpha-hydroxycarboxylic acid derivatives.

Maximilian Dochnahl1, Gregory C Fu.   

Abstract

The appropriate choice of chiral catalyst and starting materials leads to the synthesis of 1,2-oxazetidin-3-ones by cycloadditions of ketenes with nitroso compounds with very good regioselectivity and enantioselectivity. In addition to serving as potentially bioactive target molecules, the products can be transformed into other important classes of compounds, such as alpha-hydroxycarboxylic acid derivatives.

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Year:  2009        PMID: 19226588      PMCID: PMC2728616          DOI: 10.1002/anie.200805805

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  8 in total

1.  Development of bifunctional salen catalysts: rapid, chemoselective alkylations of alpha-ketoesters.

Authors:  Erin F DiMauro; Marisa C Kozlowski
Journal:  J Am Chem Soc       Date:  2002-10-30       Impact factor: 15.419

2.  Multicenter strategy for the development of catalytic enantioselective nucleophilic alkylation of ketones: Me2Zn addition to alpha-ketoesters.

Authors:  Ken Funabashi; Markus Jachmann; Motomu Kanai; Masakatsu Shibasaki
Journal:  Angew Chem Int Ed Engl       Date:  2003-11-17       Impact factor: 15.336

Review 3.  Asymmetric catalysis for the construction of quaternary carbon centres: nucleophilic addition on ketones and ketimines.

Authors:  Olivier Riant; Jérôme Hannedouche
Journal:  Org Biomol Chem       Date:  2007-02-05       Impact factor: 3.876

4.  Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds.

Authors:  Jacob M Berlin; Gregory C Fu
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

5.  Construction of enantiomerically enriched tertiary alpha-hydroxycarboxylic acid derivatives by phase-transfer-catalyzed asymmetric alkylation of diaryloxazolidin-2,4-diones.

Authors:  Takashi Ooi; Kazuhiro Fukumoto; Keiji Maruoka
Journal:  Angew Chem Int Ed Engl       Date:  2006-06-02       Impact factor: 15.336

6.  Enantioselective Staudinger synthesis of beta-lactams catalyzed by a planar-chiral nucleophile.

Authors:  Brian L Hodous; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2002-02-27       Impact factor: 15.419

7.  Asymmetric synthesis of highly substituted beta-lactones by nucleophile-catalyzed [2+2] cycloadditions of disubstituted ketenes with aldehydes.

Authors:  Jonathan E Wilson; Gregory C Fu
Journal:  Angew Chem Int Ed Engl       Date:  2004-11-26       Impact factor: 15.336

8.  Catalytic asymmetric Staudinger reactions to form beta-lactams: an unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent.

Authors:  Elaine C Lee; Brian L Hodous; Enda Bergin; Crystal Shih; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2005-08-24       Impact factor: 15.419

  8 in total
  3 in total

1.  Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition.

Authors:  Andrea M Zuhl; Justin T Mohr; Daniel A Bachovchin; Sherry Niessen; Ku-Lung Hsu; Jacob M Berlin; Maximilian Dochnahl; María P López-Alberca; Gregory C Fu; Benjamin F Cravatt
Journal:  J Am Chem Soc       Date:  2012-03-08       Impact factor: 15.419

2.  Catalytic, asymmetric reactions of ketenes and ketene enolates.

Authors:  Daniel H Paull; Anthony Weatherwax; Thomas Lectka
Journal:  Tetrahedron       Date:  2009-08-22       Impact factor: 2.457

3.  Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate.

Authors:  Gary A Molander; Livia N Cavalcanti
Journal:  J Org Chem       Date:  2012-04-24       Impact factor: 4.354

  3 in total

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