Ghent University Academic Bibliography

Advanced

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

Stijn Dekeukeleire UGent, Matthias D'hooghe UGent, Christian Müller, Dieter Vogt and Norbert De Kimpe UGent (2010) NEW JOURNAL OF CHEMISTRY. 34(6). p.1079-1083
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.
Please use this url to cite or link to this publication:
author
organization
alternative title
Rhodium-catalysed hydroformylation of N-(2-propenyl)-beta-lactams as a key step in the synthesis of functionalised N-[4-(2-oxoazetidin-1-yl)but-1-enyl]acetamides
year
type
journalArticle (original)
publication status
published
subject
keyword
BETA-LACTAMS, LACTAM SYNTHON METHOD, ASYMMETRIC-SYNTHESIS, STEREOSELECTIVE-SYNTHESIS, BUILDING-BLOCKS, STAUDINGER REACTION, TRANSFORMATION, CYCLOADDITION, MACROLIDES, COMPLEXES
journal title
NEW JOURNAL OF CHEMISTRY
New J. Chem.
volume
34
issue
6
pages
1079 - 1083
Web of Science type
Article
Web of Science id
000278275700007
JCR category
CHEMISTRY, MULTIDISCIPLINARY
JCR impact factor
2.631 (2010)
JCR rank
38/142 (2010)
JCR quartile
2 (2010)
ISSN
1144-0546
DOI
10.1039/c0nj00146e
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
1091521
handle
http://hdl.handle.net/1854/LU-1091521
date created
2010-12-22 16:11:03
date last changed
2012-01-01 00:30:28
@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 M{\"u}ller, Christian and Vogt, Dieter and De Kimpe, Norbert},
  issn         = {1144-0546},
  journal      = {NEW JOURNAL OF CHEMISTRY},
  keyword      = {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)-\ensuremath{\beta}-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},
}

Chicago
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.
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.
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.
MLA
Dekeukeleire, Stijn, Matthias D’hooghe, Christian Müller, 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 34.6 (2010): 1079–1083. Print.