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11Yakov P. NizhnikCurrent address: Department of Molecular Biology, Biological and Organic Chemistry, Petrozavodsk State University, Pr. Lenina 33, Petrozavodsk, 185910, Russia. E-mail: yakov_nizhnik@mail.ru, Jianjiang Lu, Sergiy V. RosokhaCurrent address: Department of Biological, Chemical and Physical Sciences, Roosevelt University, 430 S. Michigan Ave, Chicago, IL 60605, USA. Tel: +1 847-670-1595, Fax: +1 847-619-8555. E-mail: srosokha@roosevelt.edu. and Jay K. KochiDeceased, August 9, 2008..
Lewis acid effects on donor–acceptor associations and redox reactions: ternary complexes of heteroaromatic N-oxides with boron trifluoride and organic donors, New J. Chem., 2009, 33, 2317. M. Kumar, R. Gupta; K.-H. Hellwege, A. Hellwege (eds).
Magnetic Properties � Diamagnetic Susceptibility and Magnetic Anisotropy � Organic Compounds � Data extract from Landolt-B�rnstein II/27C: Diamagnetic Susceptibility and Magnetic Anisotropy of Organic
Compounds � Magnetic anisotropy data of C<sub>6</sub>Br<sub>4</sub>O<sub>2</sub>, Landolt-B�rnstein II/27C (2008) in SpringerMaterials Cation radicals of N-substituted phenothiazines, Chemistry of Heterocyclic Compounds Oxidative addition of tetrabromo-1,2-benzoquinone totrans-carbonylchlorobis(triphenylphosphine)rhodium andtrans-carbonyliodiobis(triphenylphosphine)rhodium, Transition Metal Chemistry Nair, V.; Radhakrishnan, K. V., Science of Synthesis, (2006) 28, 208..
Additional Methods, Science of Synthesis Chen, S.; Salo, E. C.; Kerrigan, N. J., Science of Synthesis: Asymmetric Organocatalysis, (2012) 1, 485..
o-Quinone Reactions, Science of Synthesis