Struchkov / Ikonnikov / Bilbao / Osaka / Washington DC / Tambar / New York / Saporovskaya / L. A. / Bespalova / /
Company
Peregudov A. S. / K 2 CO / Batsanov A. S. / n-Pr / Sorochinsky A. E. / Chemicals Ltd. / Creative Commons / MeI / Bn / Orlova S. A. / /
Country
Japan / United States / United Kingdom / Spain / / /
Facility
The Cambridge Crystallographic Data Centre / Stony Brook University / State University of New York / Institute of Chemical / /
IndustryTerm
target product / methanol solution / chemical shift / chemical and stereochemical outcomes / crude product / base products / final product / methyl / diastereomeric products / chemical / chemical methods / /
Movie
D. V / A. D. / A. I. / /
Organization
University of the Basque Country / National Science Foundation / Basque Government / Spanish Ministry of Science and Innovation / Stony Brook University / State University of New York / American Chemical Society / Cambridge Crystallographic Data Centre / Faculty of Chemistry / Beilstein-Institut / Basque Foundation for Science / Institute of Chemical / /
Person
Van Meervelt / Churkina / Kukhar / V / Dieter Seebach / Vadim A. Soloshonok / Dalton Trans / José Luis / Hiroki Moriwaki / / /
Position
Editor / Mp / T. D. / Corresponding author / Professor / V. P. / Experimental General / /
Product
acetic acid / /
ProvinceOrState
New Brunswick / New York / Nova Scotia / M. B. / Y. T. / /
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