Some electrophilic reactivity studies of di-(2-indolyl)dibenzofurans and di-(2-indolyl)carbazoles |
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| Institution: | 1. School of Chemistry, UNSW Australia, UNSW Sydney, NSW 2052, Australia;2. Department of Chemistry, Gebze Institute of Technology, PO Box 141, 41400 Kocaeli, Turkey;3. School of Chemistry, Faculty of Art and Science, Nam?k Kemal University, Turkey;1. Département de préhistoire/UMR 7194, Muséum national d’histoire naturelle, IPH, 1, rue René-Panhard, 75013 Paris, France;2. Chaire d’anthropologie, faculté des Lettres, université de Bohême occidentale, Sedlá?kova 15, 30614 Plzeň, République tchèque;1. Departamento de Química Inorgánica y Analítica, E.S.C.E.T., Universidad Rey Juan Carlos, 28933 Móstoles, Madrid, Spain;2. Departamento de Química, Universidad del Valle, Calle 13 No 100-00, 76001000 Cali, Colombia;3. Centro de Tecnología Repsol, Autovía de Extremadura A5, km 18, 28935 Móstoles, Madrid, Spain;1. School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan;2. National Institute of Cancer Research, National Health Research Institutes, Tainan 70456, Taiwan;3. School of Pharmacy, National Defense Medical Center, 161 Minchuan East Road, Section 6, Taipei 114, Taiwan;4. Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan;5. Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli 350, Taiwan;6. Center for Translational Medicine, Taipei Medical University, Taiwan;4. Department of Chemistry, Butler University, Indianapolis, Indiana 46208;3. Center for Structural Genomics of Infectious Diseases and the Department of Molecular Pharmacology and Biological Chemistry, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611;5. Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611;6. Department of Chemistry and Biochemistry, Loyola University Chicago, Chicago, Illinois 60660 |
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| Abstract: | 3,6-Bis-(2-indolyl)dibenzofurans 1,2, and carbazoles 3–6 underwent a range of electrophilic substitution reactions to produce formyl indoles 7–12, biindolyls 24–28 and 33–34, glyoxylamides 40–42, and amides 48. |
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| Keywords: | Bis-indoles Biindolyls Dibenzofurans Carbazoles Indole synthesis Formylation Glyoxylic amides Electrophilic substitution |
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