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Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTOccurrence, Biogenesis, and Synthesis of Biologically Active Carbazole AlkaloidsArndt W. Schmidt, Kethiri R. Reddy, and Hans-Joachim Knölker*View Author Information Department Chemie, Technische Universität Dresden, Bergstrasse 66, 01069 Dresden, Germany*E-mail: [email protected]Cite this: Chem. Rev. 2012, 112, 6, 3193–3328Publication Date (Web):April 5, 2012Publication History Received29 November 2011Published online5 April 2012Published inissue 13 June 2012https://pubs.acs.org/doi/10.1021/cr200447shttps://doi.org/10.1021/cr200447sreview-articleACS PublicationsCopyright © 2012 American Chemical SocietyRequest reuse permissionsArticle Views19925Altmetric-Citations1028LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Aromatic compounds,Chemical synthesis,Isolation,Organic compounds,Organic synthesis Get e-Alerts
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Citations
Cites
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
Miyaura, N., & Suzuki, A. (1995) · Chemical Reviews · doi:10.1021/cr00039a007 · Cited by 12,817
Sonogashira, K., Tohda, Y., & Hagihara, N. (1975) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)91094-3 · Cited by 5,208
Stille, J. K. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198605081 · Cited by 3,394
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
Ohtani, I., Kusumi, T., Kashman, Y., & Kakisawa, H. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00011a006 · Cited by 3,215
Dess, D. B., & Martin, J. C. (1983) · The Journal of Organic Chemistry · doi:10.1021/jo00170a070 · Cited by 3,114
The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry
Chinchilla, R., & Nájera, C. (2007) · Chemical Reviews · doi:10.1021/cr050992x · Cited by 2,974
Dale, J. A., & Mosher, H. S. (1973) · Journal of the American Chemical Society · doi:10.1021/ja00783a034 · Cited by 2,593
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
Ley, S. V., & Thomas, A. W. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200300594 · Cited by 2,554
Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination
Surry, D. S., & Buchwald, S. L. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200800497 · Cited by 2,016
Hartwig, J. F. (1998) · Angewandte Chemie International Edition · Cited by 1,719
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
Corey, E. J., & Fuchs, P. L. (1972) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)94157-7 · Cited by 1,583
Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products
Bringmann, G., Gulder, T., Gulder, T. A. M., & Breuning, M. (2010) · Chemical Reviews · doi:10.1021/cr100155e · Cited by 1,458
Isolation and Synthesis of Biologically Active Carbazole Alkaloids
Knölker, H., & Reddy, K. R. (2002) · Chemical Reviews · doi:10.1021/cr020059j · Cited by 1,416
Self-citationTokunaga, M., Larrow, J. F., Kakiuchi, F., & Jacobsen, E. N. (1997) · Science · doi:10.1126/science.277.5328.936 · Cited by 1,365
Medicinal Natural Products: A Biosynthetic Approach
Dewick, P. M. (2009) · Wiley eBooks · doi:10.1002/9780470742761 · Cited by 1,279
Schaus, S. E., Brandes, B. D., Larrow, J. F., Tokunaga, M., Hansen, K. B., Gould, A. E., Furrow, M. E., & Jacobsen, E. N. (2002) · Journal of the American Chemical Society · doi:10.1021/ja016737l · Cited by 1,014
Robinson, B. (1963) · Chemical Reviews · doi:10.1021/cr60224a003 · Cited by 688
Ueber die Hydrazine der Brenztraubensäure
Fischer, E., & Jourdan, F. (1883) · Berichte der deutschen chemischen Gesellschaft · doi:10.1002/cber.188301602141 · Cited by 541
New methods for the oxidation of aldehydes to carboxylic acids and esters
Corey, E. J., Gilman, N. W., & Ganem, B. E. (1968) · Journal of the American Chemical Society · doi:10.1021/ja01022a059 · Cited by 502
Palladium-Catalysed Reactions of Organotin Compounds
Mitchell, T. N. (1992) · Synthesis · doi:10.1055/s-1992-26230 · Cited by 491
Indolocarbazole natural products: occurrence, biosynthesis, and biological activity
Sánchez, C., Méndez, C., & Salas, J. A. (2006) · Nat. Prod. Rep. · doi:10.1039/b601930g · Cited by 407
Studies on the Fischer indole synthesis
Robinson, B. (1969) · Chemical Reviews · doi:10.1021/cr60258a004 · Cited by 384
Indolo[3,2-b]carbazole-Based Thin-Film Transistors with High Mobility and Stability
Wu, Y., Li, Y., Gardner, S., & Ong, B. S. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0456149 · Cited by 349
Discovery of a Proneurogenic, Neuroprotective Chemical
Pieper, A. A., Xie, S., Capota, E., Estill, S. J., Zhong, J., Long, J. M., Becker, G. L., Huntington, P., Goldman, S. E., Shen, C.-H., et al. (2010) · Cell · doi:10.1016/j.cell.2010.06.018 · Cited by 347
Name Reactions in Heterocyclic Chemistry
(2004) · Wiley eBooks · doi:10.1002/0471704156 · Cited by 291
Production and biological activity of rebeccamycin, a novel antitumor agent.
BUSH, J. A., LONG, B. H., CATINO, J. J., & BRADNER, W. T. (1987) · The Journal of Antibiotics · doi:10.7164/antibiotics.40.668 · Cited by 252
Rickards, R. W., Rothschild, J. M., Willis, A. C., de Chazal, N. M., Kirk, J., Kirk, K., Saliba, K. J., & Smith, G. D. (1999) · Tetrahedron · doi:10.1016/s0040-4020(99)00833-9 · Cited by 249
Ding, L., Münch, J., Goerls, H., Maier, A., Fiebig, H.-H., Lin, W.-H., & Hertweck, C. (2010) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2010.09.010 · Cited by 237
Ruthenium Half‐Sandwich Complexes Bound to Protein Kinase Pim‐1
Debreczeni, J. É., Bullock, A. N., Atilla, G. E., Williams, D. S., Bregman, H., Knapp, S., & Meggers, E. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200503468 · Cited by 234
Alkaloids of Ochrosia elliptica Labill.1
Goodwin, S., Smith, A. F., & Horning, E. C. (1959) · Journal of the American Chemical Society · doi:10.1021/ja01517a031 · Cited by 232
The Biosynthetic Gene Cluster for the Antitumor Rebeccamycin
Sánchez, C., Butovich, I. A., Braña, A. F., Rohr, J., Méndez, C., & Salas, J. A. (2002) · Chemistry & Biology · doi:10.1016/s1074-5521(02)00126-6 · Cited by 218
Staurosporine, a Potentially Important Gift from a Microorganism.
OMURA, S., SASAKI, Y., IWAI, Y., & TAKESHIMA, H. (1995) · The Journal of Antibiotics · doi:10.7164/antibiotics.48.535 · Cited by 216
Witulski, B., & Alayrac, C. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020902)41:17<3281::aid-anie3281>3.0.co;2-g · Cited by 214
Chemical biology of natural indolocarbazole products: 30 years since the discovery of staurosporine
Nakano, H., & Ōmura, S. (2009) · The Journal of Antibiotics · doi:10.1038/ja.2008.4 · Cited by 203
New Principles in Medicinal Organometallic Chemistry
Schatzschneider, U., & Metzler‐Nolte, N. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200504604 · Cited by 194
A family of multicyclic indolosesquiterpenes from a bacterial endophyte
Ding, L., Maier, A., Fiebig, H.-H., Lin, W.-H., & Hertweck, C. (2011) · Organic & Biomolecular Chemistry · doi:10.1039/c1ob05283g · Cited by 191
UCN-01, a selective inhibitor of protein kinase C from Streptomyces.
TAKAHASHI, I., KOBAYASHI, E., ASANO, K., YOSHIDA, M., & NAKANO, H. (1987) · The Journal of Antibiotics · doi:10.7164/antibiotics.40.1782 · Cited by 186
Iridium Complex with Antiangiogenic Properties
Wilbuer, A., Vlecken, D. H., Schmitz, D. J., Kräling, K., Harms, K., Bagowski, C. P., & Meggers, E. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201000682 · Cited by 168
Tjipanazoles, new antifungal agents from the blue-green alga Tolypothrix tjipanasensis
Bonjouklian, R., Smitka, T. A., Doolin, L. E., Molloy, R. M., Debono, M., Shaffer, S. A., Moore, R. E., Stewart, J. B., & Patterson, G. M. L. (1991) · Tetrahedron · doi:10.1016/s0040-4020(01)81932-3 · Cited by 158
TAKAHASHI, I., Saitoh, Y., Yoshida, M., Sano, H., Nakano, H., Morimoto, M., & Tamaoki, T. (1989) · The Journal of Antibiotics · doi:10.7164/antibiotics.42.571 · Cited by 158
Protein kinase inhibition of clinically important staurosporine analogues
Gani, O. A. B. S. M., & Engh, R. A. (2010) · Natural Product Reports · doi:10.1039/b923848b · Cited by 154
Lynamicins A−E, Chlorinated Bisindole Pyrrole Antibiotics from a Novel Marine Actinomycete
McArthur, K., Mitchell, S. S., Tsueng, G., Rheingold, A. L., White, D. J., Grodberg, J., Lam, K. S., & Potts, B. C. M. (2008) · Journal of Natural Products · doi:10.1021/np800286d · Cited by 151
The anticancer agent ellipticine on activation by cytochrome P450 forms covalent DNA adducts☆
Stiborová, M., Bieler, C. A., Wießler, M., & Frei, E. (2001) · Biochemical Pharmacology · doi:10.1016/s0006-2952(01)00806-1 · Cited by 150
Coumarins and Carbazoles fromClausena excavataExhibited Antimycobacterial and Antifungal Activities
Sunthitikawinsakul, A., Kongkathip, N., Kongkathip, B., Phonnakhu, S., Daly, J. W., Spande, T. F., Nimit, Y., & Rochanaruangrai, S. (2003) · Planta Medica · doi:10.1055/s-2003-37716 · Cited by 147
Yamashita, Y., Fujii, N., Murakata, C., Ashizawa, T., Okabe, M., & Nakano, H. (1992) · Biochemistry · doi:10.1021/bi00163a015 · Cited by 145
Paoletti, C., Pecq, J. B. L., Xuong, N. D., Juret, P., Garnier, H., Amiel, J.-L., & Rouëssé, J. (1980) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-642-81488-4_15 · Cited by 144
Warabi, K., Matsunaga, S., van Soest, R. W. M., & Fusetani, N. (2003) · The Journal of Organic Chemistry · doi:10.1021/jo0267910 · Cited by 143
Stokes, B. J., Richert, K. J., & Driver, T. G. (2009) · The Journal of Organic Chemistry · doi:10.1021/jo901224k · Cited by 136
Stiborová, M., Sejbal, J., Bořek-Dohalská, L., Aimová, D., Poljaková, J., Forsterová, K., Rupertová, M., Wiesner, J., Hudeček, J., Wießler, M., et al. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2202 · Cited by 132
Onaka, H., TANIFGUCHI, S.-I., Igarashi, Y., & FURUMAI, T. (2002) · The Journal of Antibiotics · doi:10.7164/antibiotics.55.1063 · Cited by 131
Berlinck, R. G. S., Britton, R., Piers, E., Lim, L., Roberge, M., da Rocha, R. M., & Andersen, R. J. (1998) · The Journal of Organic Chemistry · doi:10.1021/jo981607p · Cited by 128
An Organometallic Inhibitor for Glycogen Synthase Kinase 3
Bregman, H. S., Williams, D. S., Atilla, G. E., Carroll, P. J., & Meggers, E. (2004) · Journal of the American Chemical Society · doi:10.1021/ja046049c · Cited by 127
Salas, A. P., Zhu, L., Sánchez, C., Braña, A. F., Rohr, J., Méndez, C., & Salas, J. A. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04777.x · Cited by 122
Recent progress in the chemistry and applications of indolocarbazoles
Janosik, T., Wahlström, N., & Bergman, J. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.06.101 · Cited by 121
Onaka, H., TANIGUCHI, S.-I., Igarashi, Y., & FURUMAI, T. (2003) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.67.127 · Cited by 115
Thevissen, K., Marchand, A., Chaltin, P., Meert, E. M. K., & Cammue, B. P. A. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709788612701 · Cited by 115
Palmer, B. D., Thompson, A. M., Booth, R. J., Dobrusin, E. M., Kraker, A. J., Lee, H. H., Lunney, E. A., Mitchell, L. H., Ortwine, D. F., Smaill, J. B., et al. (2006) · Journal of Medicinal Chemistry · doi:10.1021/jm0512591 · Cited by 112
Claurailas A−D, Cytotoxic Carbazole Alkaloids from the Roots of Clausena harmandiana
Songsiang, U., Thongthoom, T., Boonyarat, C., & Yenjai, C. (2011) · Journal of Natural Products · doi:10.1021/np100654m · Cited by 111
Synthesis, Electrochemistry, and Bioactivity of the Cyanobacterial Calothrixins and Related Quinones
Bernardo, P. H., Chai, C. L. L., Heath, G. A., Mahon, P. J., Smith, G. D., Waring, P., & Wilkes, B. (2004) · Journal of Medicinal Chemistry · doi:10.1021/jm049625o · Cited by 109
Total Syntheses of the Telomerase Inhibitors Dictyodendrin B, C, and E
Fürstner, A., Domostoj, M. M., & Scheiper, B. (2006) · Journal of the American Chemical Society · doi:10.1021/ja0617800 · Cited by 109
Total Synthesis of Dictyodendrin B
Fürstner, A., Domostoj, M. M., & Scheiper, B. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0541175 · Cited by 108
TAKAHASHI, I., Asano, K., Kawamoto, I., Tamaoki, T., & Nakano, H. (1989) · The Journal of Antibiotics · doi:10.7164/antibiotics.42.564 · Cited by 107
Cytotoxic, antiviral indolocarbazoles from a blue-green alga belonging to the nostocaceae.
Knübel, G., Larsen, L. K., Moore, R. E., Levine, I. A., & Patterson, G. M. L. (1990) · The Journal of Antibiotics · doi:10.7164/antibiotics.43.1236 · Cited by 104
Calothrixins, a New Class of Human DNA Topoisomerase I Poisons
Khan, Q. A., Lu, J., & Hecht, S. M. (2009) · Journal of Natural Products · doi:10.1021/np8007232 · Cited by 104
Total Synthesis of Dictyodendrin A and B
Okano, K., Fujiwara, H., Noji, T., Fukuyama, T., & Tokuyama, H. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201001966 · Cited by 104
Siamenol, a New Carbazole Alkaloid from Murraya siamensis
Meragelman, K. M., McKee, T. C., & Boyd, M. R. (2000) · Journal of Natural Products · doi:10.1021/np990570g · Cited by 99
Woodward, R. B., Iacobucci, G. A., & Hochstein, I. A. (1959) · Journal of the American Chemical Society · doi:10.1021/ja01525a085 · Cited by 99
Zhu, G., Conner, S. E., Zhou, X., Shih, C., Li, T., Anderson, B. D., Brooks, H. B., Campbell, R. M., Considine, E. L., Dempsey, J. A., et al. (2003) · Journal of Medicinal Chemistry · doi:10.1021/jm0256169 · Cited by 96
Kato, S., Kawai, H., KAWASAKI, T., et al. (1989) · The Journal of Antibiotics · doi:10.7164/antibiotics.42.1879 · Cited by 94
Recent Developments of Rebeccamycin Analogues as Topoisomerase I Inhibitors and Antitumor Agents.
Prudhomme, M. (2000) · Current Medicinal Chemistry · doi:10.2174/0929867003374138 · Cited by 94
First total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant
Alayrac, C., Schollmeyer, D., & Witulski, B. (2009) · Chemical Communications · doi:10.1039/b820291e · Cited by 92
Similar Biological Activities of Two Isostructural Ruthenium and Osmium Complexes
Maksimoska, J., Williams, D. S., Atilla‐Gokcumen, G. E., Smalley, K. S. M., Carroll, P. J., Webster, R. D., Filippakopoulos, P., Knapp, S., Herlyn, M., & Meggers, E. (2008) · Chemistry - A European Journal · doi:10.1002/chem.200800294 · Cited by 89
A New Radical-Based Route to Calothrixin B
Bennasar, M.-L., Roca, T., & Ferrando, F. (2006) · Organic Letters · doi:10.1021/ol052600e · Cited by 87
A new total synthesis of an indolo[3,2-j]phenanthridine alkaloid calothrixin B
Tohyama, S., Choshi, T., Matsumoto, K., Yamabuki, A., 池方康一郎, Nobuhiro, J., & Hibino, S. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.06.042 · Cited by 84
Bergman, J., Janosik, T., & Wahlström, N. (2001) · Advances in heterocyclic chemistry · doi:10.1016/s0065-2725(01)80012-x · Cited by 83
Human cancer cell (Jurkat) killing by the cyanobacterial metabolite calothrixin A
Chen, X., Smith, G. D., & Waring, P. (2003) · Journal of Applied Phycology · doi:10.1023/a:1025134106985 · Cited by 82
New Tryptophan Metabolites from Cultures of the Lipophilic Yeast Malassezia furfur
Irlinger, B., Bartsch, A., Krämer, H., Mayser, P. A., & Steglich, W. (2005) · Helvetica Chimica Acta · doi:10.1002/hlca.200590118 · Cited by 82
Mechanism of mahanine-induced apoptosis in human leukemia cells (HL-60)
Roy, M. K., Thalang, V. N., Trakoontivakorn, G., & Nakahara, K. (2003) · Biochemical Pharmacology · doi:10.1016/j.bcp.2003.07.021 · Cited by 81
Al‐Trawneh, S. A., Zahra, J. A., Kamal, M. R., et al. (2010) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2010.06.098 · Cited by 78
Cardellina, J. H., Kirkup, M. P., Moore, R. E., et al. (1979) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)86748-4 · Cited by 77
Unusual Sulfamate Indoles and a Novel Indolo[3,2-a]carbazole from Ancorina sp.1
Meragelman, K. M., West, L. M., Northcote, P. T., Pannell, L. K., McKee, T. C., & Boyd, M. R. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo020120k · Cited by 74
Isolation and Identification of "Diazepam-Like" Compounds From Bovine Urine
Luk, K.-C., Stern, L., Weigele, M., et al. (1983) · Journal of Natural Products · doi:10.1021/np50030a005 · Cited by 73
Concise and Efficient Synthesis of Calothrixin B
Sissouma, D., Maingot, L., Collet, S., & Guingant, A. Y. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo061270o · Cited by 73
Gu, R., Hameurlaine, A., & Dehaen, W. (2007) · The Journal of Organic Chemistry · doi:10.1021/jo0711337 · Cited by 69
Total Synthesis of Dictyodendrins A–E
Tokuyama, H., Okano, K., Fujiwara, H., Noji, T., & Fukuyama, T. (2010) · Chemistry - An Asian Journal · doi:10.1002/asia.201000544 · Cited by 68
Synthesis of carbazoles by dehydro Diels–Alder reactions of ynamides
Martínez-Esperón, M. F., Rodrı́guez, D., Castedo, L., & Saá, C. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.02.029 · Cited by 68
11-Hydroxystaurosporine: a highly cytotoxic, powerful protein kinase C inhibitor from a tunicate
Kinnel, R. B., & Scheuer, P. J. (1992) · The Journal of Organic Chemistry · doi:10.1021/jo00049a049 · Cited by 68
Jagadeesh, S., Sinha, S., Pal, B. C., Bhattacharya, S., & Banerjee, P. P. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.08.005 · Cited by 67
Wright, A. D., Papendorf, O., & König, G. M. (2005) · Journal of Natural Products · doi:10.1021/np049640w · Cited by 67
Synthesis of the Potent Antimalarials Calothrixin A and B
Kelly, T. R., Zhao, Y., Cavero, M., & Torneiro, M. (2000) · Organic Letters · doi:10.1021/ol006649q · Cited by 67
A biomimetic synthesis of the indolo[3,2-j]phenanthridine alkaloid, calothrixin B
Yamabuki, A., Fujinawa, H., Choshi, T., Tohyama, S., Matsumoto, K., Ohmura, K., Nobuhiro, J., & Hibino, S. (2006) · Tetrahedron Letters · doi:10.1016/j.tetlet.2006.06.077 · Cited by 66
Sánchez, C., Salas, A. P., Braña, A. F., Palomino‐Schätzlein, M., Pineda‐Lucena, A., Carbajo, R. J., Méndez, C., Morís, F., & Salas, J. A. (2009) · Chemical Communications · doi:10.1039/b905068j · Cited by 66
Wu, S. J., Fotso, S., Li, F., Qin, S., Kelter, G., Fiebig, H., & Laatsch, H. (2006) · The Journal of Antibiotics · doi:10.1038/ja.2006.46 · Cited by 65
Friedel−Crafts Acylation and Metalation Strategies in the Synthesis of Calothrixins A and B
Bernardo, P. H., & Chai, C. L. L. (2003) · The Journal of Organic Chemistry · doi:10.1021/jo035049c · Cited by 65
Concise Total Synthesis of Calothrixins A and B
Abe, T., Ikeda, T., Yanada, R., & Ishikura, M. (2011) · Organic Letters · doi:10.1021/ol201107a · Cited by 65
Fan, G., Li, Z., Shen, S. H., Zeng, Y., Yang, Y., Xu, M.-J., Bruhn, T., Bruhn, H. D., Morschhäuser, J., Bringmann, G., et al. (2010) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2010.06.052 · Cited by 64
Optical rotatory dispersion and circular dichroism or aromatic compounds: a general survey
Crabbé, P., & Klyne, W. (1967) · Tetrahedron · doi:10.1016/s0040-4020(01)92310-5 · Cited by 64
Staurosporine aglycone (K252-c) and arcyriaflavin A from the marine ascidian,Eudistoma sp
Horton, P. A., Longley, R. E., McConnell, O. J., et al. (1994) · Cellular and Molecular Life Sciences · doi:10.1007/bf01956468 · Cited by 63
Tietze, L. F., Singidi, R. R., Gericke, K. M., Böckemeier, H., & Laatsch, H. (2007) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200700534 · Cited by 62
Dhayalan, V., Clement, J. A., Jagan, R., & Mohanakrishnan, A. K. (2008) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200801018 · Cited by 62
Synthetic Studies on Indolocarbazoles: Total Synthesis of Staurosporine Aglycon
Rajeshwaran, G. G., & Mohanakrishnan, A. K. (2011) · Organic Letters · doi:10.1021/ol200094b · Cited by 62
Novel, potent and selective cyclin D1/CDK4 inhibitors: indolo[6,7-a]pyrrolo[3,4-c]carbazoles
Engler, T. A., Furness, K., Malhotra, S., Sánchez-Martínez, C., Shih, C., Xie, W., Zhu, G., Zhou, X., Conner, S. E., Faul, M. M., et al. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00461-x · Cited by 60
Piers, E., Britton, R., & Andersen, R. J. (1999) · The Journal of Organic Chemistry · doi:10.1021/jo9914723 · Cited by 60
Sur les principes constituants de l'Illicium religiosum (Sieb.) (Shikimi‐no‐ki en japonais)
Eijkman, J. F. (1885) · Recueil des Travaux Chimiques des Pays-Bas · doi:10.1002/recl.18850040202 · Cited by 59
Purpurone, an inhibitor of ATP-citrate lyase: a novel alkaloid from the marine sponge Iotrochota sp
Chan, G. W., Francis, T. A., Thureen, D. R., Offen, P. H., Pierce, N. J., WESTLEY, J. W., Johnson, R. K., & Faulkner, D. J. (1993) · The Journal of Organic Chemistry · doi:10.1021/jo00061a031 · Cited by 59
Synthesis-driven mapping of the dictyodendrin alkaloids
Buchgraber, P., Domostoj, M. M., Scheiper, B., Wirtz, C., MYNOTT, R. J., Rust, J., & Fürstner, A. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.06.058 · Cited by 58
The Biosynthetic Origins of Rebeccamycin
Pearce, C. J., Doyle, T. W., Forenza, S., et al. (1988) · Journal of Natural Products · doi:10.1021/np50059a020 · Cited by 57
The structure of tubingensin B: A cytotoxic carbazole alkaloid from the sclerotia of
TePaske, M. R., Gloer, J. B., Wicklow, D. T., & Dowd, P. F. (1989) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)93829-8 · Cited by 57
KOJIRI, K., KONDO, H., Yoshinari, T., Arakawa, H., Nakajima, S., SATOH, F., KAWAMURA, K., Okura, A., Suda, H., & OKANISHI, M. (1991) · The Journal of Antibiotics · doi:10.7164/antibiotics.44.723 · Cited by 57
Aryl[a]pyrrolo[3,4-c]carbazoles as selective cyclin D1-CDK4 inhibitors
Sánchez-Martı́nez, C., Shih, C., Faul, M. M., Zhu, G., Paal, M., Somoza, C., Li, T., Kumrich, C. A., Winneroski, L. L., Zhou, X., et al. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00791-1 · Cited by 56
Cañedo, L. M., Blanco, J. A. D. L. F., BAZ, J. P., PUENTES, J. L. F., MILLÁN, F. R., Espliego‐Vazquez, F., Fernandez‐Chimeno, R. I., & GRAVALOS, D. G. (2000) · The Journal of Antibiotics · doi:10.7164/antibiotics.53.895 · Cited by 55
Increasing the Kinase Specificity of K252a by Protein Surface Recognition
Schneider, T. L., Mathew, R. S., Rice, K. P., Tamaki, K., Wood, J. L., & Schepartz, A. (2005) · Organic Letters · doi:10.1021/ol050179o · Cited by 52
Zhou, Y., & Verkade, J. G. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200900846 · Cited by 52
Roy, M. K., Thalang, V. N., Trakoontivakorn, G., & Nakahara, K. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706137 · Cited by 52
Stress induced carbazole phytoalexins in Glycosmis species
Pacher, T., Bacher, M., Hofer, O., & Greger, H. (2001) · Phytochemistry · doi:10.1016/s0031-9422(01)00186-8 · Cited by 51
Metabolism Studies of Indole Derivatives Using a Staurosporine Producer,Streptomyces staurosporeus
Yang, S., & Cordell, G. A. (1997) · Journal of Natural Products · doi:10.1021/np960566u · Cited by 51
ZHD-0501, a novel naturally occurring staurosporine analog from Actinomadura sp. 007
Xiao-xian, H., Cui, C., Gu, Q., Zhu, W., Liu, H., Gu, J., & Osada, H. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.06.154 · Cited by 51
Engineering biosynthetic pathways to generate antitumor indolocarbazole derivatives
Sánchez, C., Méndez, C., & Salas, J. A. (2006) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-006-0092-5 · Cited by 48
Satheeshkumar, N., Mukherjee, P. K., Bhadra, S., Saha, B. P., & Pal, B. C. (2009) · Phytotherapy Research · doi:10.1002/ptr.3023 · Cited by 47
Nair, V., Nandialath, V., Abhilash, K. G., & Suresh, E. (2008) · Organic & Biomolecular Chemistry · doi:10.1039/b803009j · Cited by 46
A simple and concise route to calothrixin B
Bernardo, P. H., Chai, C. L. L., & Elix, J. A. (2002) · Tetrahedron Letters · doi:10.1016/s0040-4039(02)00434-3 · Cited by 45
A formal total synthesis of the telomerase inhibitor dictyodendrin B
Hirao, S., Yoshinaga, Y., Iwao, M., & Ishibashi, F. (2009) · Tetrahedron Letters · doi:10.1016/j.tetlet.2009.11.083 · Cited by 45
McErlean, C. S. P., Sperry, J., Blake, A. J., & Moody, C. J. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.08.057 · Cited by 45
Nakatani, S., Naoe, A., Yamamoto, Y., Yamauchi, T., Yamaguchi, N., & Ishibashi, M. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00592-4 · Cited by 44
Progress towards the Total Synthesis of the Bioactive Calothrixins A and B
Hibino, S., & Choshi, T. (2009) · Heterocycles · doi:10.3987/rev-08-sr(f)2 · Cited by 44
Synthesis of the pyrrolo[2,3-c]carbazole core of the dictyodendrins
Ayats, C., Soley, R., Alberício, F., & Álvarez, M. (2009) · Organic & Biomolecular Chemistry · doi:10.1039/b822933n · Cited by 43
Sánchez-Martı́nez, C., Shih, C., Zhu, G., Li, T., Brooks, H. B., Patel, B. K. R., Schultz, R. M., DeHahn, T. B., Spencer, C. D., Watkins, S. A., et al. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00792-3 · Cited by 43
Asamizu, S., Kato, Y., Igarashi, Y., FURUMAI, T., & Onaka, H. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.11.061 · Cited by 42
A biomimetic synthesis of calothrixin B
Sperry, J., McErlean, C. S. P., Slawin, A. M. Z., & Moody, C. J. (2006) · Tetrahedron Letters · doi:10.1016/j.tetlet.2006.11.053 · Cited by 40
Total Synthesis of Bioactive Indolo[3,2-j]phenanthridine Alkaloid, Calothrixin B
Hibino, S., Choshi, T., Tohyama, S., Matsumoto, K., Yamabuki, A., Hieda, Y., & Nobuhiro, J. (2010) · Heterocycles · doi:10.3987/com-10-s(e)11 · Cited by 39
Poly(N-acylethylenimines) with pendant carbazole derivatives. 1. Synthesis
Hsieh, B. R., & Litt, M. H. (1985) · Macromolecules · doi:10.1021/ma00149a006 · Cited by 38
Li, E., Xu, X., Li, H., Zhang, H., Xu, X., Yuan, X., & Li, Y. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.08.075 · Cited by 38
Smaill, J. B., Baker, E. N., Booth, R. J., Bridges, A. J., Dickson, J. M. J. J., Dobrusin, E. M., Ivanović, I., Kraker, A. J., Lee, H. H., Lunney, E. A., et al. (2007) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2007.07.016 · Cited by 35
An efficient modification of ellipticine synthesis and preparation of 13-hydroxyellipticine
Dračínský, M., Sejbal, J., Rygerová, B., & Stiborová, M. (2007) · Tetrahedron Letters · doi:10.1016/j.tetlet.2007.07.160 · Cited by 34
Horaguchi, T., Oyanagi, T., Creencia, E. C., et al. (2004) · Journal of Heterocyclic Chemistry · doi:10.1002/jhet.5570410101 · Cited by 33
Mevalonic acid a precursor of the substituted benzenoid ring of -anthraquinones
Leistner, E. W., & Zenk, M. H. (1968) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)98961-0 · Cited by 32
Further Minor Metabolites of Staurosporine Produced by a Streptomyces longisporofiavus Strain.
CAI, Y., Fredenhagen, A., Hug, P., Meyer, T., & PETER, H. H. (1996) · The Journal of Antibiotics · doi:10.7164/antibiotics.49.519 · Cited by 27
Murrayakoeninol- A New Carbazole Alkaloid from Murraya Koenigii (Linn) Spreng
Chakraborty, M., Saha, S., & Mukhapadhyay, S. (2009) · Natural Product Communications · doi:10.1177/1934578x0900400309 · Cited by 27
Hugon, B., Pfeiffer, B., Renard, P., & Prudhomme, M. (2003) · Tetrahedron Letters · doi:10.1016/s0040-4039(03)00924-9 · Cited by 25
A one pot synthesis of annulated carbazole analogs
Mohanakrishnan, A. K., Dhayalan, V., Clement, J. A., Sureshbabu, R. B. R., & Kumar, N. S. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.07.036 · Cited by 24
Lee, H., Chen, G. S., Chen, C., et al. (2010) · Journal of Heterocyclic Chemistry · doi:10.1002/jhet.319 · Cited by 23
Synthesis of functionalized ellipticinium and ellipticine derivatives via electrophilic cyclization
Chaitanya, T. K., & Nagarajan, R. (2011) · Organic & Biomolecular Chemistry · doi:10.1039/c1ob05258f · Cited by 23
O- andN-Methylation in the Biosynthesis of Staurosporine
Yang, S., Lin, L.-J., Cordell, G. A., Wang, P., & Corley, D. G. (1999) · Journal of Natural Products · doi:10.1021/np990261q · Cited by 21
Gruner, K. K., & Knölker, H. (2011) · Wiley eBooks · doi:10.1002/9783527634880.ch10 · Cited by 16
Self-citationCAI, Y., Fredenhagen, A., Hug, P., & PETER, H. H. (1996) · The Journal of Antibiotics · doi:10.7164/antibiotics.49.1060 · Cited by 13
Chaitanya, T. K., Prakash, K. S., & Nagarajan, R. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.06.076 · Cited by 13
Hill, R. A. (2010) · Annual Reports Section B (Organic Chemistry) · doi:10.1039/b927083n · Cited by 13
Carbon catabolite regulation of rebeccamycin production inSaccharothrix aerocolonigenes
Lam, K. S., MATTEI, J. M., & Forenza, S. (1989) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/bf01569794 · Cited by 12
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Metadata
- Authors
- Schmidt, A. W., Reddy, K. R., & Knölker, H.-J.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-04-05
- Volume
- 112
- Issue
- 6
- Pages
- 3193-3328
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2016978898
- Cited by
- 1,243
- References
- 148
- FWCI
- 5.60
- Type
- journal article
- Language
- en
- Open access
- closed
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