Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)–O and Ni(II)–N coordination bonds

Vadim A. Soloshonok, José Luis Aceña, Hisanori Ueki and Jianlin Han
Beilstein J. Org. Chem. 2012, 8, 1920–1928. https://doi.org/10.3762/bjoc.8.223

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Supporting Information File 1: NMR spectra of compounds 14b and 19/20.
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Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)–O and Ni(II)–N coordination bonds
Vadim A. Soloshonok, José Luis Aceña, Hisanori Ueki and Jianlin Han
Beilstein J. Org. Chem. 2012, 8, 1920–1928. https://doi.org/10.3762/bjoc.8.223

How to Cite

Soloshonok, V. A.; Aceña, J. L.; Ueki, H.; Han, J. Beilstein J. Org. Chem. 2012, 8, 1920–1928. doi:10.3762/bjoc.8.223

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  • Han, J.; Aceña, J. L.; Yasuda, N.; Uekusa, H.; Ono, T.; Soloshonok, V. A.; Klika, K. D. Carbonyl group coordination preferences in square-planar NiII and PdII complexes of pentadentate ligands by electron-withdrawing/donating substituents. Inorganica Chimica Acta 2015, 433, 3–12. doi:10.1016/j.ica.2015.04.029
  • Acena, J. L.; Sorochinsky, A. E.; Soloshonok, V. A. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations. Amino acids 2014, 46, 2047–2073. doi:10.1007/s00726-014-1764-5
  • Han, J.; Ono, T.; Uekusa, H.; Klika, K. D.; Soloshonok, V. A. Substituent-controlled preference of carbonyl group-metal coordination in d8 metal complexes with non-symmetric pentadentate ligands. Structural and stereochemical aspects. Dalton transactions (Cambridge, England : 2003) 2014, 43, 5375–5381. doi:10.1039/c3dt53312c
  • Moriwaki, H.; Resch, D.; Li, H.; Ojima, I.; Takeda, R.; Aceña, J. L.; Soloshonok, V. A. Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)amino]acetyl}amino)benzophenone; a case of configurationally stable stereogenic nitrogen. Beilstein journal of organic chemistry 2014, 10, 442–448. doi:10.3762/bjoc.10.41
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