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- Infrared study of the Beckmann rearrangement catalysed by decationated zeolite. J. D. Butler, T. C. Poles
, J. Chem. Soc., Perkin Trans. 2
, 1973
, 41
- Beckmann rearrangement of cyclopentanone oxime catalysed by decationated zeolite. John D. Butler, Terence C. Poles
, J. Chem. Soc., Perkin Trans. 2
, 1973
, 1262
- 278. Nucleotides. Part XXXV. cycloPentanone oxime p-nitro-benzenesulphonate as an intermediate in the synthesis of nucleotide derivatives : an alternative synthesis of adenosine-5′ triphosphate. B. H. Chase, G. W. Kenner, Alexander R. Todd, R. F. Webb
, J. Chem. Soc.
, 1956
, 1371
- Cyclopenta-1,2,3-dithiazoles and related compounds. M. John Plater, Charles W. Rees, David G. Roe, Tomás Torroba
, J. Chem. Soc., Perkin Trans. 1
, 1993
, 769
- 255. Studies on phosphorylation. Part XIII. Ketoxime sulphonates as intermediates in pyrophosphate formation. G. W. Kenner, Alexander R. Todd, R. F. Webb
, J. Chem. Soc.
, 1956
, 1231
- Site selectivity in the addition of ketoximes to activated allenes and alkynes; N- versus
O-alkylation. Frances Heaney, Bronwyn M. Kelly, Sharon Bourke, Oliver Rooney, Desmond Cunningham, Patrick McArdle
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 143
- A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones. Victor-Emmanuel H. Kassin, Romain Morodo, Thomas Toupy, Isaline Jacquemin, Kristof Van Hecke, Raphaël Robiette, Jean-Christophe M. Monbaliu
, Green Chem.
, 2021
, 23
, 2336
- Oxime rearrangements: ab initio calculations and reactions in the solid state. Vesna Šimunić-Mežnarić, Zlatko Mihalić, Hrvoj Vančik
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 2154
- Ring fused 1,2,5-thiadiazoles from oximes and trithiazyl trichloride. Charles W. Rees, Tai-Yuen Yue
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 2538
- A novel oxime to pentathiepin cascade reaction. Sonia Macho, Charles W. Rees, Teresa Rodríguez, Tomás Torroba
, Chem. Commun.
, 2001
, 403