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Rhodium-catalysed hydroformylation of N-(2-propenyl)-β-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides

(2010) NEW JOURNAL OF CHEMISTRY. 34(6). p.1079-1083
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Abstract
Biologically relevant functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides have been prepared in a two-step approach starting from N-(2-propenyl)-beta-lactams, involving initial rhodium-catalysed hydroformylation followed by subjection of the obtained aldehydes to Staudinger reaction conditions after initial imination.
Keywords
BETA-LACTAMS, LACTAM SYNTHON METHOD, ASYMMETRIC-SYNTHESIS, STEREOSELECTIVE-SYNTHESIS, BUILDING-BLOCKS, STAUDINGER REACTION, TRANSFORMATION, CYCLOADDITION, MACROLIDES, COMPLEXES

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Citation

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MLA
Dekeukeleire, Stijn, et al. “Rhodium-Catalysed Hydroformylation of N-(2-Propenyl)-β-Lactams as a Key Step in the Synthesis of Functionalised N-[4-(2-Oxoazetidin-1-Yl)but-1-Enyl]Acetamides.” NEW JOURNAL OF CHEMISTRY, vol. 34, no. 6, 2010, pp. 1079–83, doi:10.1039/c0nj00146e.
APA
Dekeukeleire, S., D’hooghe, M., Müller, C., Vogt, D., & De Kimpe, N. (2010). Rhodium-catalysed hydroformylation of N-(2-propenyl)-β-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides. NEW JOURNAL OF CHEMISTRY, 34(6), 1079–1083. https://doi.org/10.1039/c0nj00146e
Chicago author-date
Dekeukeleire, Stijn, Matthias D’hooghe, Christian Müller, Dieter Vogt, and Norbert De Kimpe. 2010. “Rhodium-Catalysed Hydroformylation of N-(2-Propenyl)-β-Lactams as a Key Step in the Synthesis of Functionalised N-[4-(2-Oxoazetidin-1-Yl)but-1-Enyl]Acetamides.” NEW JOURNAL OF CHEMISTRY 34 (6): 1079–83. https://doi.org/10.1039/c0nj00146e.
Chicago author-date (all authors)
Dekeukeleire, Stijn, Matthias D’hooghe, Christian Müller, Dieter Vogt, and Norbert De Kimpe. 2010. “Rhodium-Catalysed Hydroformylation of N-(2-Propenyl)-β-Lactams as a Key Step in the Synthesis of Functionalised N-[4-(2-Oxoazetidin-1-Yl)but-1-Enyl]Acetamides.” NEW JOURNAL OF CHEMISTRY 34 (6): 1079–1083. doi:10.1039/c0nj00146e.
Vancouver
1.
Dekeukeleire S, D’hooghe M, Müller C, Vogt D, De Kimpe N. Rhodium-catalysed hydroformylation of N-(2-propenyl)-β-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides. NEW JOURNAL OF CHEMISTRY. 2010;34(6):1079–83.
IEEE
[1]
S. Dekeukeleire, M. D’hooghe, C. Müller, D. Vogt, and N. De Kimpe, “Rhodium-catalysed hydroformylation of N-(2-propenyl)-β-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides,” NEW JOURNAL OF CHEMISTRY, vol. 34, no. 6, pp. 1079–1083, 2010.
@article{1091521,
  abstract     = {{Biologically relevant functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides have been prepared in a two-step approach starting from N-(2-propenyl)-beta-lactams, involving initial rhodium-catalysed hydroformylation followed by subjection of the obtained aldehydes to Staudinger reaction conditions after initial imination.}},
  author       = {{Dekeukeleire, Stijn and D'hooghe, Matthias and Müller, Christian and Vogt, Dieter and De Kimpe, Norbert}},
  issn         = {{1144-0546}},
  journal      = {{NEW JOURNAL OF CHEMISTRY}},
  keywords     = {{BETA-LACTAMS,LACTAM SYNTHON METHOD,ASYMMETRIC-SYNTHESIS,STEREOSELECTIVE-SYNTHESIS,BUILDING-BLOCKS,STAUDINGER REACTION,TRANSFORMATION,CYCLOADDITION,MACROLIDES,COMPLEXES}},
  language     = {{eng}},
  number       = {{6}},
  pages        = {{1079--1083}},
  title        = {{Rhodium-catalysed hydroformylation of N-(2-propenyl)-β-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides}},
  url          = {{http://dx.doi.org/10.1039/c0nj00146e}},
  volume       = {{34}},
  year         = {{2010}},
}

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