Synthesis of Cyano-pyrrolo[1,2-a][1,10]phenanthroline Derivatives Using a Multicomponent Condensation
1,10‐Phenanthroline reacts with malonitrile and aldehydes in the presence of isocyanides as domino‐Knoevenagel‐nucleophilic cycloaddition for generation of a new class of 10‐(aryl)‐11‐(alkyl‐ or arylamino‐)pyrrolo[1,2‐a][1,10]phenanthroline‐9‐carbonitrile compounds in excellent yield. All compounds...
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| Veröffentlicht in: | Journal of heterocyclic chemistry 2013-05, Vol.50 (3), p.568-572 |
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| container_end_page | 572 |
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| container_issue | 3 |
| container_start_page | 568 |
| container_title | Journal of heterocyclic chemistry |
| container_volume | 50 |
| creator | Marandi, Ghasem Hazeri, Nourallah Maghsoodlou, Malek T. Habibi-Khorassani, Sayyed M. Torbati, Niloufar Akbarzadeh Rostami-Charati, Faramarz Skelton, Brian W. Makha, Mohamed |
| description | 1,10‐Phenanthroline reacts with malonitrile and aldehydes in the presence of isocyanides as domino‐Knoevenagel‐nucleophilic cycloaddition for generation of a new class of 10‐(aryl)‐11‐(alkyl‐ or arylamino‐)pyrrolo[1,2‐a][1,10]phenanthroline‐9‐carbonitrile compounds in excellent yield. All compounds are fully characterized with one structurally authenticated by a single X‐ray diffraction study. |
| doi_str_mv | 10.1002/jhet.1532 |
| format | Article |
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| ispartof | Journal of heterocyclic chemistry, 2013-05, Vol.50 (3), p.568-572 |
| issn | 0022-152X 1943-5193 |
| language | eng |
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| source | Wiley Online Library Journals Frontfile Complete |
| subjects | Condensation Diffraction X-rays |
| title | Synthesis of Cyano-pyrrolo[1,2-a][1,10]phenanthroline Derivatives Using a Multicomponent Condensation |
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