caa a22 4500 445878835 CHVBK 20180317145536.0 cr unu---uuuuu 170323e20111101xx s 000 0 eng 10.1007/s11030-011-9316-3 doi (NATIONALLICENCE)springer-10.1007/s11030-011-9316-3 Lithium perchlorate-nitromethane-promoted alkylation of anilines with arylmethanols [Elektronische Daten] [Jun Zhou, Hai-Feng Mao, Lu Wang, Jian-Ping Zou, Wei Zhang] A new application of lithium perchlorate-nitromethane (LPNM) for the formation of aromatic C-N and C-C bonds is introduced. LPNM-promoted reactions of anilines with diarylmethanols selectively generate N-alkylated anilines or mono and double Friedel-Crafts alkylation products under different conditions by changing the reaction time, reaction temperature, and the ratio of the reactants. This method does not require the use of transition metal catalysts to prepare alkylated aniline derivatives. Springer Science+Business Media B.V., 2011 Lithium perchlorate-nitromethane nationallicence Anilines nationallicence Arylmethanols nationallicence N -alkylation nationallicence Friedel-Crafts alkylation nationallicence Zhou Jun Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut Mao Hai-Feng Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut Wang Lu Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut Zou Jian-Ping Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut Zhang Wei Department of Chemistry, University of Massachusetts Boston, 100 Morrissey Blvd., 02125, Boston, MA, USA aut Molecular Diversity Springer Netherlands 15/4(2011-11-01), 849-855 1381-1991 15:4<849 2011 15 11030 https://doi.org/10.1007/s11030-011-9316-3 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/s11030-011-9316-3 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Zhou Jun Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut NATIONALLICENCE 700 1- Mao Hai-Feng Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut NATIONALLICENCE 700 1- Wang Lu Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut NATIONALLICENCE 700 1- Zou Jian-Ping Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, 199 Renai Street, 215123, Suzhou, Jiangsu, China aut NATIONALLICENCE 700 1- Zhang Wei Department of Chemistry, University of Massachusetts Boston, 100 Morrissey Blvd., 02125, Boston, MA, USA aut NATIONALLICENCE 773 0- Molecular Diversity Springer Netherlands 15/4(2011-11-01), 849-855 1381-1991 15:4<849 2011 15 11030 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer