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- General method for the asymmetric synthesis of α-amino acids via alkylation of the chiral nickel(II) Schiff base complexes of glycine and alanine. Yuri. N. Belokon, Vladimir I. Bakhmutov, Nina I. Chernoglazova, Konstantin A. Kochetkov, Sergei V. Vitt, Natalia S. Garbalinskaya, Vasili M. Belikov
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 305
- Two new monofunctional platinum(ii) dithiocarbamate complexes: phenanthriplatin-type axial protection, equatorial-axial conformational isomerism, and anticancer and DNA binding studies. Muhammad Imran, Zia ur Rehman, Graeme Hogarth, Derek A. Tocher, Gul-e-Saba Chaudhry, Ian S. Butler, Francine Bélanger-Gariepy, Tamara Kondratyuk
, Dalton Trans.
, 2020
, 49
, 15385
- LXXXIV.—The influence of solvents, etc., on the rotation of optically active compounds. Part XXI. The relationship of the rotatory powers of ethyl tartrate, isobutyl tartrate and isobutyl diacetyltartrate. Thomas Stewart Patterson
, J. Chem. Soc., Trans.
, 1916
, 109
, 1139
- 119. Synthetic antimalarials. Part XXIII. 2-Arylguanidino-4-aminoalkylaminopyrimidines. Further variations. W. H. Cliffe, F. H. S. Curd, F. L. Rose, M. Scott
, J. Chem. Soc.
, 1948
, 574
- 836. The crystal structure of trans-oxotrichlorobisdiethylphenylphosphinerhenium(V). H. W. W. Ehrlich, P. G. Owston
, J. Chem. Soc.
, 1963
, 4368
- 663. The scope and mechanism of carbohydrate osotriazole formation. Part VIII. Azo-dyes from aminophenylosotriazoles. H. El Khadem, G. H. Labib, M. H. Meshreki
, J. Chem. Soc.
, 1963
, 3528
- Infrared intensities as a quantitative measure of intramolecular interactions. Part XXXII. Conjugation of the substituent and the triple bond in monosubstituted acetylenes. T. Bruce Grindley, Keith F. Johnson, Alan R. Katritzky, Henry J. Keogh, Christine Thirkettle, Robert T. C. Brownlee, John A. Munday, Ronald D. Topsom
, J. Chem. Soc., Perkin Trans. 2
, 1974
, 276
- Group 4 organometallic compounds. Part 8. Preparation and Mössbauer spectra of five- and six-co-ordinate di- and tri-organotin compounds containing mixed phenyl and butyl groups on tin. V. G. Kumar Das, Ng Seik Weng, Peter J. Smith, Robin Hill
, J. Chem. Soc., Dalton Trans.
, 1981
, 552
- Acid–base equilibria of substituted benzoic acids. Part I. J. M. Wilson, N. E. Gore, J. E. Sawbridge, F. Cardenas-Cruz
, J. Chem. Soc. B
, 1967
, 852
- Hydration changes upon protein unfolding: cosolvent effect analysis. Hassan O. Hammou, Isabel M. Plaza del Pino, Jose M. Sanchez-Ruiz
, New J. Chem.
, 1998
, 22
, 1453