caa a22 4500 445878347 CHVBK 20180317145534.0 cr unu---uuuuu 170323e20110201xx s 000 0 eng 10.1007/s11030-010-9254-5 doi (NATIONALLICENCE)springer-10.1007/s11030-010-9254-5 Synthesis of cyano-2,3-dihydropyrrolo[1,2- f ]phenanthridine derivatives via a domino-Knoevenagel-cyclization [Elektronische Daten] [Ghasem Marandi, Malek Maghsoodlou, Nourallah Hazeri, Sayyed Habibi-Khorassani, Niloufar Torbati, Faramarz Rostami-Charati, Brian Skelton, Mohamed Makha] In a new multicomponent reaction phenanthridine reacts with isocyanides and malonitrile in the presence of benzaldehyde derivatives to produce 2-aryl-3-(alkyl- or arylimino)-2,3-dihydropyrrolo[1,2-f]phenanthridine-1,1(12b H)-dicarbonitrile in a simple, mild, and efficient protocol in excellent yields. Graphical Abstract: Springer Science+Business Media B.V., 2010 Phenanthridine nationallicence Isocyanides nationallicence Malonitrile nationallicence Benzaldehyde derivatives nationallicence MCR nationallicence Multicomponent nationallicence Knoevenagel nationallicence Marandi Ghasem Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut Maghsoodlou Malek Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut Hazeri Nourallah Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut Habibi-Khorassani Sayyed Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut Torbati Niloufar Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut Rostami-Charati Faramarz Gonbad Institutes of Higher Education, P.O. Box 163, Gonbad, Iran aut Skelton Brian Chemistry School of Biomedical, Biomolecular and Chemical Science, M313, University of Western Australia, 6009, Perth, WA, Australia aut Makha Mohamed Chemistry School of Biomedical, Biomolecular and Chemical Science, M313, University of Western Australia, 6009, Perth, WA, Australia aut Molecular Diversity Springer Netherlands 15/1(2011-02-01), 197-201 1381-1991 15:1<197 2011 15 11030 https://doi.org/10.1007/s11030-010-9254-5 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/s11030-010-9254-5 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Marandi Ghasem Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut NATIONALLICENCE 700 1- Maghsoodlou Malek Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut NATIONALLICENCE 700 1- Hazeri Nourallah Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut NATIONALLICENCE 700 1- Habibi-Khorassani Sayyed Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut NATIONALLICENCE 700 1- Torbati Niloufar Department of Chemistry, The University of Sistan & Baluchestan, P.O. Box 98135-674, Zahedan, Iran aut NATIONALLICENCE 700 1- Rostami-Charati Faramarz Gonbad Institutes of Higher Education, P.O. Box 163, Gonbad, Iran aut NATIONALLICENCE 700 1- Skelton Brian Chemistry School of Biomedical, Biomolecular and Chemical Science, M313, University of Western Australia, 6009, Perth, WA, Australia aut NATIONALLICENCE 700 1- Makha Mohamed Chemistry School of Biomedical, Biomolecular and Chemical Science, M313, University of Western Australia, 6009, Perth, WA, Australia aut NATIONALLICENCE 773 0- Molecular Diversity Springer Netherlands 15/1(2011-02-01), 197-201 1381-1991 15:1<197 2011 15 11030 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer