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Metal-catalysed reactions of imines with ethyl diazoacetate leading to
aziridines
. Kaare G. Rasmussen, Karl Anker Jørgensen
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 1287
- Reduction of 2-chloro-N-phenylpropanamide and 2-methyl-N-phenylaziridine with lithium aluminium hydride. Mie Højer Vilhelmsen, Lars Frøsig Østergaard, Mogens Brøndsted Nielsen, Steen Hammerum
, Org. Biomol. Chem.
, 2008
, 6
, 1773
- Molecular polarisability. The conformation of N-phenylaziridine. R. S. Armstrong, M. J. Aroney, R. J. W. Le Fèvre, H. J. Stootman, W. Lüttke
, J. Chem. Soc. B
, 1971
, 2104
- Ring opening reactions of 2-trialkylsilylaziridines. Alan R. Bassindale, Patricia A. Kyle, Marie-Claire Soobramanien, Peter G. Taylor
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 439
- The synthesis of 2-trialkylsilylaziridines from vinyltrialkylsilanes or the reaction of α-chloro-α-silyl carbanions with imines. Alan R. Bassindale, Patricia A. Kyle, Marie-Claire Soobramanien, Peter G. Taylor
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 1173
- Intramolecular reactions. Part X. Transition states in the cyclisation of N-ω-halogeno-alkylamines and sulphonamides. Roger Bird, Anthony C. Knipe, Charles J. M. Stirling
, J. Chem. Soc., Perkin Trans. 2
, 1973
, 1215
- N-(2-Methoxycarbonyl-2-yloethyl)phenylaminyl:
EPR observation of a triplet nonconjugated 1,3-diradical with two different
kinds of radical centers. Hideyuki Tukada
, Chem. Commun.
, 2000
, 63
- Organoantimony and organobismuth complexes for CO2 fixation. Yi Chen, Renhua Qiu, Xinhua Xu, Chak-Tong Au, Shuang-Feng Yin
, RSC Adv.
, 2014
, 4
, 11907
- Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-β-lactams and study of their ring opening. Matthias D'hooghe, Karen Mollet, Stijn Dekeukeleire, Norbert De Kimpe
, Org. Biomol. Chem.
, 2010
, 8
, 607
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Microwave-assisted regioselective ring opening of non-activated aziridines by lithium aluminium hydride. Sonja Stanković, Matthias D'hooghe, Norbert De Kimpe
, Org. Biomol. Chem.
, 2010
, 8
, 4266