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- Role of the solvent in optical resolution of trans-chrysanthemic acid via diastereomeric salt formation with (1R,2R)-1-(4-nitrophenyl)-2-dimethylaminopropane-1,3-diol. Éva Kozsda-Kovács, György Miklós Keserü, György Miklós Keserü, Zsolt Böcskei, Ildikó Szilágyi, Kálmán Simon, Béla Bertók, Elemér Fogassy
, J. Chem. Soc., Perkin Trans. 2
, 2000
, 149
- A stereoselective synthesis of trans-chrysanthemic acid. R. W. Mills, R. D. H. Murray, R. A. Raphael
, J. Chem. Soc. D
, 1971
, 555a
- The same and not the same. Similarities and differences in the resolution of
trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols. Goffredo Rosini, Claudia Ayoub, Valerio Borzatta, Emanuela Marotta, Andrea Mazzanti, Paolo Righi
, Green Chem.
, 2007
, 9
, 441
- 948. Synthesis, absolute configuration, and ring-fission of cis- and trans-homocaronic acid: their configurative relation to natural terpenes. L. Crombie, J. Crossley, D. A. Mitchard
, J. Chem. Soc.
, 1963
, 4957
- A new stereoselective synthesis of trans-chrysanthemic acid [2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylic acid]. R. W. Mills, R. D. H. Murray, R. A. Raphael
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 133
- Absolute configuration of (+)-trans-chrysanthemic acid. Crystal structure analysis of a p-bromoanilide derivative. A. Forbes Cameron, George Ferguson, Christine Hannaway
, J. Chem. Soc., Perkin Trans. 2
, 1975
, 1567
- Quantitative determination of the enantiomeric purity of synthetic pyrethroids. Part I. The chrysanthemic acid moiety. F. E. Rickett
, Analyst
, 1973
, 98
, 687
- Quantitative determination of the enantiomeric purity of synthetic pyrethroids. Part II. S-bioallethrin. F. E. Rickett, P. B. Henry
, Analyst
, 1974
, 99
, 330
- p
1,n
1 Salts: self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid. Goffredo Rosini, Claudia Ayoub, Valerio Borzatta, Andrea Mazzanti, Emanuela Marotta, Paolo Righi
, Chem. Commun.
, 2006
, 4294
- The racemate cage. Influence of p
1,n
1
salt occurrence on enantiomer separation processes. The case of
trans-chrysanthemic acid. Goffredo Rosini, Valerio Borzatta, Francesca Boschi, Gabriele Candido, Emanuela Marotta, Paolo Righi
, Chem. Commun.
, 2007
, 2717