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Volumn 15, Issue 7, 2011, Pages 1036-1057

Isolation, biological activities and synthesis of indoloquinoline alkaloids: Cryptolepine, isocryptolepine and neocryptolepine

Author keywords

Alkaloid; Cryptolepine; Heteroaromatic; Indoloquinoline; Isocryptolepine and neocryptolepine

Indexed keywords

BIOACTIVITY; METABOLITES; SYNTHESIS (CHEMICAL);

EID: 79952760286     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211794785118     Document Type: Review
Times cited : (85)

References (116)
  • 2
    • 0030754049 scopus 로고    scopus 로고
    • In Vitro and in Vivo Antiplasmodial Activity of Cryptolepine and Related Alkaloids from Cryptolepis sanguinolenta
    • Cimanga, K.; De Bruyne, T.; Pieters, L.; Vlietinck, A. J.; Turger, C. A. In Vitro and in Vivo Antiplasmodial Activity of Cryptolepine and Related Alkaloids from Cryptolepis sanguinolenta. J. Nat. Prod., 1997, 60, 688.
    • (1997) J. Nat. Prod , vol.60 , pp. 688
    • Cimanga, K.1    de Bruyne, T.2    Pieters, L.3    Vlietinck, A.J.4    Turger, C.A.5
  • 3
    • 0033963121 scopus 로고    scopus 로고
    • Antiplasmodial Activity of Cryptolepis sanguinolenta Alkaloids from Leaves and Roots
    • Paulo, A.; Gomes, E. T.; Steele, J.; Warhurst, D. C.; Houghton, P. J. Antiplasmodial Activity of Cryptolepis sanguinolenta Alkaloids from Leaves and Roots. Planta Med., 2000, 66, 30.
    • (2000) Planta Med , vol.66 , pp. 30
    • Paulo, A.1    Gomes, E.T.2    Steele, J.3    Warhurst, D.C.4    Houghton, P.J.5
  • 5
    • 85200013084 scopus 로고    scopus 로고
    • Website of the World Health Organization, Accessed Jan. 05, 2010
    • Website of the World Health Organization: http://www.who.int/en/ (Accessed Jan. 05, 2010).
  • 6
  • 8
    • 0025000310 scopus 로고
    • 1HNMR and 13C-NMR Assignments of Cryptolepine, A 3:4-Benz-α-carboline Derivative Isolated from Cryptolepis sanguinolenta
    • Ablordeppey, S. D.; Hufford, C. D.; Bourne, R. F.; Dwama-Badu, D. 1HNMR and 13C-NMR Assignments of Cryptolepine, A 3:4-Benz-α-carboline Derivative Isolated from Cryptolepis sanguinolenta. Planta Med., 1990, 56, 416.
    • (1990) Planta Med , vol.56 , pp. 416
    • Ablordeppey, S.D.1    Hufford, C.D.2    Bourne, R.F.3    Dwama-Badu, D.4
  • 12
    • 84986533271 scopus 로고
    • Total Assignment of the Proton and Carbon NMR Spectra of the Alkaloid Quindoline-Utilization of HMQC-TOCSY to Indirectly Establish Protonated Carbon-Protonated Carbon Connectivities
    • Spitzer, T. D.; Crouch, R. C.; Martin, G. E.; Sharaf, M. H. M.; Schiff, P. L. Jr.; Tackie, A. N.; Boye, G. L. Total Assignment of the Proton and Carbon NMR Spectra of the Alkaloid Quindoline-Utilization of HMQC-TOCSY to Indirectly Establish Protonated Carbon-Protonated Carbon Connectivities. J. Heterocycl. Chem., 1991, 28, 2065.
    • (1991) J. Heterocycl. Chem , vol.28 , pp. 2065
    • Spitzer, T.D.1    Crouch, R.C.2    Martin, G.E.3    Sharaf, M.H.M.4    Schiff Jr., P.L.5    Tackie, A.N.6    Boye, G.L.7
  • 14
    • 0029060768 scopus 로고
    • Elucidation of the Structure of Quindolinone, a Minor Alkaloid of Cryptolepis sanguinolenta: Submiligram 1H-13C and 1H-15N Heteronuclear Shift Correlation Experiments Using Micro Inverse-Detection
    • Crouch, R. C.; Davis, A. O.; Spitzer, T. D.; Martin, G. E.; Sharaf, M. H. M.; Schiff, P. L. Jr.; Phoebe, C. H. Jr.; Tackie, A. N. Elucidation of the Structure of Quindolinone, a Minor Alkaloid of Cryptolepis sanguinolenta: Submiligram 1H-13C and 1H-15N Heteronuclear Shift Correlation Experiments Using Micro Inverse-Detection. J. Heterocycl. Chem., 1995, 32, 1077.
    • (1995) J. Heterocycl. Chem , vol.32 , pp. 1077
    • Crouch, R.C.1    Davis, A.O.2    Spitzer, T.D.3    Martin, G.E.4    Sharaf, M.H.M.5    Schiff Jr., P.L.6    Phoebe Jr., C.H.7    Tackie, A.N.8
  • 15
    • 0029561490 scopus 로고
    • New Alkaloids from Cryptolepis sanguinolenta
    • Paulo, A.; Gomes, E. T.; Hougton, P. J. New Alkaloids from Cryptolepis sanguinolenta. J. Nat. Prod., 1995, 58, 1485.
    • (1995) J. Nat. Prod , vol.58 , pp. 1485
    • Paulo, A.1    Gomes, E.T.2    Hougton, P.J.3
  • 16
    • 0032425654 scopus 로고    scopus 로고
    • Isolation and Unambiguous Synthesis of Cryptolepinone: An Oxidation Artifact of Cryptolepine
    • Fort, D. M.; Litvak, J.; Chen, J. L.; Lu, Q.; Phuan, P. W.; Cooper, R.; Bierer, D. E. Isolation and Unambiguous Synthesis of Cryptolepinone: An Oxidation Artifact of Cryptolepine. J. Nat. Prod., 1998, 61, 1528.
    • (1998) J. Nat. Prod , vol.61 , pp. 1528
    • Fort, D.M.1    Litvak, J.2    Chen, J.L.3    Lu, Q.4    Phuan, P.W.5    Cooper, R.6    Bierer, D.E.7
  • 21
    • 84990739945 scopus 로고
    • Antimicrobial Properties of Some West African Plants
    • Boakye-Yiadom, K. Antimicrobial Properties of Some West African Plants. Quart. J. Crude Drug Res. 1979, 17, 78.
    • (1979) Quart. J. Crude Drug Res , vol.17 , pp. 78
    • Boakye-Yiadom, K.1
  • 24
    • 84979189660 scopus 로고
    • Ueber Chindolin. (Over Quindoline)
    • Fichter, F.; Boehringer, R. Ueber Chindolin. (Over Quindoline). Chem. Ber., 1906, 39, 3932.
    • (1906) Chem. Ber , vol.39 , pp. 3932
    • Fichter, F.1    Boehringer, R.2
  • 25
    • 0001202061 scopus 로고
    • Sur la composition chimique de Cryptolepis triangularies. Plante congolaise
    • Clinquart, E. Sur la composition chimique de Cryptolepis triangularies. Plante congolaise. (On the Chemical Composition of Cryptolepis triangularies. Plants from the (Belgian) Congo). Bull. Acad. R. Med. Belg., 1929, 9, 627.
    • (1929) Bull. Acad. R. Med. Belg , vol.9 , pp. 627
    • Clinquart, E.1
  • 26
    • 0029975674 scopus 로고    scopus 로고
    • Two New Indoloquinoline Alkaloids from Cryptolepis sanguinolenta: Cryptosanguinolentine and Cryptotackieine
    • Sharaf, M. H. M.; Schiff, P. L. Jr.; Tackie, A. N.; Phoebe, C. H. Jr.; Martin, G. E. Two New Indoloquinoline Alkaloids from Cryptolepis sanguinolenta: Cryptosanguinolentine and Cryptotackieine. J. Heterocycl. Chem., 1996, 33, 239.
    • (1996) J. Heterocycl. Chem , vol.33 , pp. 239
    • Sharaf, M.H.M.1    Schiff Jr., P.L.2    Tackie, A.N.3    Phoebe Jr., C.H.4    Martin, G.E.5
  • 31
    • 0035866694 scopus 로고    scopus 로고
    • New Synthesis of Benzo-δ-carbolines, Cryptolepines, and Their Salts: In Vitro Cytotoxic, Antiplasmodial, and Antitrypanosomal Activities of δ-Carbolines, Benzo-δ-carbolines, and Cryptolepines
    • Arzel, E.; Rocca, P.; Grellier, P.; Labaeid, M.; Frappier, F.; Gueritte, F.; Gaspard, C.; Marsais, F.; Godard, A.; Queguiner, G. New Synthesis of Benzo-δ-carbolines, Cryptolepines, and Their Salts: In Vitro Cytotoxic, Antiplasmodial, and Antitrypanosomal Activities of δ-Carbolines, Benzo-δ-carbolines, and Cryptolepines. J. Med. Chem., 2001, 44, 949.
    • (2001) J. Med. Chem , vol.44 , pp. 949
    • Arzel, E.1    Rocca, P.2    Grellier, P.3    Labaeid, M.4    Frappier, F.5    Gueritte, F.6    Gaspard, C.7    Marsais, F.8    Godard, A.9    Queguiner, G.10
  • 34
    • 0036008538 scopus 로고    scopus 로고
    • Crystallization and preliminary X- ray analysis of the antimalarial and cytotoxic alkaloid cryptolepine complexed with the DNA fragment d(CCTAGG)2
    • Lisgarten, J. N.; Pous, J.; Coll, M.; Wright, C. W.; Aymami, J. Crystallization and preliminary X- ray analysis of the antimalarial and cytotoxic alkaloid cryptolepine complexed with the DNA fragment d(CCTAGG)2. Acta Crystallogr. D Biol. Crystallogr., 2002, 58, 312.
    • (2002) Acta Crystallogr. D Biol. Crystallogr , vol.58 , pp. 312
    • Lisgarten, J.N.1    Pous, J.2    Coll, M.3    Wright, C.W.4    Aymami, J.5
  • 35
    • 0029129352 scopus 로고
    • In vitro and in vivo antimalarial activity of cryptolepine, a plant-derived Indoloquinoline
    • Kirby, G. C.; Paine, A.; Warhurst, D. C.; Noamese, B. K.; Phillipson, J. D. In vitro and in vivo antimalarial activity of cryptolepine, a plant-derived Indoloquinoline. Phytother. Res., 1995, 9, 359.
    • (1995) Phytother. Res , vol.9 , pp. 359
    • Kirby, G.C.1    Paine, A.2    Warhurst, D.C.3    Noamese, B.K.4    Phillipson, J.D.5
  • 36
    • 0028114917 scopus 로고
    • Synthesis and Structure-Activity Relationship of Methyl-Substituted Indolo[2,3- b]quinolines: Novel Cytotoxic, DNA Topoisomerase II Inhibitors
    • Peczynska-Czoch, W.; Pognan, F.; Kaczmarek, L.; Boratynski, J. Synthesis and Structure-Activity Relationship of Methyl-Substituted Indolo[2,3- b]quinolines: Novel Cytotoxic, DNA Topoisomerase II Inhibitors. J. Med. Chem., 1994, 37, 3503.
    • (1994) J. Med. Chem , vol.37 , pp. 3503
    • Peczynska-Czoch, W.1    Pognan, F.2    Kaczmarek, L.3    Boratynski, J.4
  • 37
    • 0000179037 scopus 로고    scopus 로고
    • Antibacterial and antifungal activities of neocryptolepine, biscryptolepine and cryptoquindoline, alkaloids isolated from Cryptolepis sanguinolenta
    • Cimanga, K.; De Bruyne, T.; Pieters, L.; Totte, J.; Tona, L.; Kambu, K.; Berghe, D.-V.; Vlietinck, A. J. Antibacterial and antifungal activities of neocryptolepine, biscryptolepine and cryptoquindoline, alkaloids isolated from Cryptolepis sanguinolenta. Phytomedicine, 1998, 5, 209.
    • (1998) Phytomedicine , vol.5 , pp. 209
    • Cimanga, K.1    de Bruyne, T.2    Pieters, L.3    Totte, J.4    Tona, L.5    Kambu, K.6    Berghe, D.-V.7    Vlietinck, A.J.8
  • 38
    • 0032977368 scopus 로고    scopus 로고
    • Probing the N-5 region of the indoloquinoline alkaloid, cryptolepine for anticryptococcal activity
    • Abblordeppey, S. Y.; Fan, P.; Clark, A. M.; Nimrod, A. Probing the N-5 region of the indoloquinoline alkaloid, cryptolepine for anticryptococcal activity. Bioorg. Med. Chem., 1999, 7, 343.
    • (1999) Bioorg. Med. Chem , vol.7 , pp. 343
    • Abblordeppey, S.Y.1    Fan, P.2    Clark, A.M.3    Nimrod, A.4
  • 39
    • 73449103586 scopus 로고    scopus 로고
    • Recent Applications of Palladium-Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries
    • Torborg, C.; Beller, M. Recent Applications of Palladium-Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries. Adv. Synth. Catal., 2009, 351, 3027.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 3027
    • Torborg, C.1    Beller, M.2
  • 40
    • 33846893890 scopus 로고    scopus 로고
    • Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts
    • Yin, L.; Liebscher, J. Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts. Chem. Rev., 2007, 107, 133.
    • (2007) Chem. Rev , vol.107 , pp. 133
    • Yin, L.1    Liebscher, J.2
  • 41
    • 33645865241 scopus 로고    scopus 로고
    • On the Nature of the Active Species in Palladium Catalyzed Mizoroki-Heck and Suzuki-Miyaura Couplings - Homogeneous or Heterogeneous Catalysis, A Critical Review
    • Phan, N. T. S.; Van Der Sluys, M.; Jones, C. W. On the Nature of the Active Species in Palladium Catalyzed Mizoroki-Heck and Suzuki-Miyaura Couplings - Homogeneous or Heterogeneous Catalysis, A Critical Review. Adv. Synth. Catal., 2006, 348, 609.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 609
    • Phan, N.T.S.1    van der Sluys, M.2    Jones, C.W.3
  • 42
    • 22744442306 scopus 로고    scopus 로고
    • Palladium-Catalyzed Cross-Coupling Reactions in Total Synthesis
    • Nicolau, K. C.; Bulger, P. G.; Sarlah, D. Palladium-Catalyzed Cross-Coupling Reactions in Total Synthesis. Angew. Chem. Int. Ed., 2005, 44, 4442.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 4442
    • Nicolau, K.C.1    Bulger, P.G.2    Sarlah, D.3
  • 43
    • 12444340794 scopus 로고    scopus 로고
    • High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview
    • Farina, V. High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview. Adv. Synth. Catal., 2004, 346, 1553.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1553
    • Farina, V.1
  • 44
    • 0038305874 scopus 로고    scopus 로고
    • A Convenient Synthesis of Two New Indoloquinoline Alkaloids
    • Timari, G.; Soos, T.; Hajos, G. A Convenient Synthesis of Two New Indoloquinoline Alkaloids. Synlett, 1997, 1067.
    • (1997) Synlett , pp. 1067
    • Timari, G.1    Soos, T.2    Hajos, G.3
  • 45
    • 0031418357 scopus 로고    scopus 로고
    • An Alternative Synthesis of 10H-Indolo[3,2-b]quinoline and its Selective N-Alkylation
    • Fan, P.; Ablordeppey, S. Y. An Alternative Synthesis of 10H-Indolo[3,2-b]quinoline and its Selective N-Alkylation. J. Heterocycl. Chem., 1997, 34, 1789.
    • (1997) J. Heterocycl. Chem , vol.34 , pp. 1789
    • Fan, P.1    Ablordeppey, S.Y.2
  • 46
    • 0032171307 scopus 로고    scopus 로고
    • First halogendance reaction in quinoline series: Application to a new synthesis of quindoline
    • Arzel, E.; Rocca, P.; Marsais, F.; Godard, A.; Queguiner, G. First halogendance reaction in quinoline series: application to a new synthesis of quindoline. Tetrahedron Lett., 1998, 39, 6465.
    • (1998) Tetrahedron Lett , vol.39 , pp. 6465
    • Arzel, E.1    Rocca, P.2    Marsais, F.3    Godard, A.4    Queguiner, G.5
  • 47
    • 0027751860 scopus 로고
    • First metalation of aryl iodides: Directed ortholithiation of iodopyridines, halogen- dance, and application to synthesis
    • Rocca, P.; Cochennec, C.; Marsais, F.; Thomas-dit-Dumont, L.; Mallet, M.; Godard, A.; Queguiner, G. First metalation of aryl iodides: directed ortholithiation of iodopyridines, halogen- dance, and application to synthesis. J. Org. Chem., 1993, 58, 7832.
    • (1993) J. Org. Chem , vol.58 , pp. 7832
    • Rocca, P.1    Cochennec, C.2    Marsais, F.3    Thomas-dit-Dumont, L.4    Mallet, M.5    Godard, A.6    Queguiner, G.7
  • 48
    • 84947151032 scopus 로고
    • The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
    • Miyaura, N.; Yanagi, T.; Suzuki, A. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases. Synth. Commun., 1981, 513.
    • (1981) Synth. Commun , pp. 513
    • Miyaura, N.1    Yanagi, T.2    Suzuki, A.3
  • 49
    • 0030604627 scopus 로고    scopus 로고
    • Metalation in Connection with Cross-coupling Reactions. Coupling of Hindered Aryls for the Synthesis of 4-Phenylpyridines as Part of Streptonigrin and Lavendamycin Analogues
    • Godard, A.; Rocca, P.; Pomel, V.; Thomas-dit-Dumont, L.; Rovera, J. C.; Thaburet, J. F.; Marsais, F.; Queguiner, G. Metalation in Connection with Cross-coupling Reactions. Coupling of Hindered Aryls for the Synthesis of 4-Phenylpyridines as Part of Streptonigrin and Lavendamycin Analogues. J. Organomet. Chem., 1996, 517, 25.
    • (1996) J. Organomet. Chem , vol.517 , pp. 25
    • Godard, A.1    Rocca, P.2    Pomel, V.3    Thomas-dit-Dumont, L.4    Rovera, J.C.5    Thaburet, J.F.6    Marsais, F.7    Queguiner, G.8
  • 50
    • 39749179066 scopus 로고    scopus 로고
    • Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: A critical overview. Part 2: The Suzuki reaction
    • Alonso, F.; Beletskaya, I. P.; Yus, M. Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: a critical overview. Part 2: The Suzuki reaction. Tetrahedron, 2008, 64, 3047.
    • (2008) Tetrahedron , vol.64 , pp. 3047
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 51
    • 7644241634 scopus 로고    scopus 로고
    • Palladium Catalysts for the Suzuki Cross- Coupling Reaction: An Overview of Recent Advances
    • Bellina, F.; Carpita, A.; Rossi, R. Palladium Catalysts for the Suzuki Cross- Coupling Reaction: An Overview of Recent Advances. Synthesis, 2004, 2419.
    • (2004) Synthesis , pp. 2419
    • Bellina, F.1    Carpita, A.2    Rossi, R.3
  • 52
    • 0027389998 scopus 로고
    • Connection between metalation and cross- coupling strategies. A new convergent route to azacarbazoles
    • Rocca, P.; Marsais, F.; Godard, A.; Queguiner, G. Connection between metalation and cross- coupling strategies. A new convergent route to azacarbazoles. Tetrahedron, 1993, 1, 49.
    • (1993) Tetrahedron , vol.1 , pp. 49
    • Rocca, P.1    Marsais, F.2    Godard, A.3    Queguiner, G.4
  • 54
    • 0037968590 scopus 로고    scopus 로고
    • An alternative synthesis of quindoline and one of its closely related derivatives
    • Csanyi, D.; Timari, G.; Hajos, G. An alternative synthesis of quindoline and one of its closely related derivatives. Synth. Commun., 1999, 29, 3959.
    • (1999) Synth. Commun , vol.29 , pp. 3959
    • Csanyi, D.1    Timari, G.2    Hajos, G.3
  • 55
    • 84918112388 scopus 로고
    • Reactivity of 2,3-, 2,4-, and 3,4-Dibromoquinoline Towards Potassium Amide in Liquid Ammonia
    • Hertog, H. J.; Buurman, D. J. Reactivity of 2,3-, 2,4-, and 3,4-Dibromoquinoline Towards Potassium Amide in Liquid Ammonia. Recl. Trav. Chim. Pays-Bas, 1973, 304, 305.
    • (1973) Recl. Trav. Chim. Pays-Bas , vol.304 , pp. 305
    • Hertog, H.J.1    Buurman, D.J.2
  • 56
    • 0012534767 scopus 로고    scopus 로고
    • Exploitation of differential reactivity of the carbon-chlorine bonds in 1,3-dichloroisoquinoline. Routes to new N,Nchelate ligands and 1,3-disubstituted isoquinolines
    • Ford, A.; Sinn, E.; Woodward, S. Exploitation of differential reactivity of the carbon-chlorine bonds in 1,3-dichloroisoquinoline. Routes to new N,Nchelate ligands and 1,3-disubstituted isoquinolines. J. Chem. Soc., Perkin Trans. 1, 1997, 927.
    • (1997) J. Chem. Soc., Perkin Trans , vol.1 , pp. 927
    • Ford, A.1    Sinn, E.2    Woodward, S.3
  • 58
    • 33748656316 scopus 로고    scopus 로고
    • Recent developments in aromatic heteroatom coupling reactions
    • Frost, C. G.; Mendonca, P. Recent developments in aromatic heteroatom coupling reactions. J. Chem. Soc., Perkin Trans. 1, 1998, 2615.
    • (1998) J. Chem. Soc., Perkin Trans , vol.1 , pp. 2615
    • Frost, C.G.1    Mendonca, P.2
  • 59
    • 0000157513 scopus 로고    scopus 로고
    • Practical Palladium Catalysts for C-N and C-O Bond Formation
    • Muci, A. R.; Buchwald, S. L. Practical Palladium Catalysts for C-N and C-O Bond Formation. Top. Curr. Chem., 2002, 219, 131.
    • (2002) Top. Curr. Chem , vol.219 , pp. 131
    • Muci, A.R.1    Buchwald, S.L.2
  • 60
    • 31544469241 scopus 로고    scopus 로고
    • Industrial-Scale Palladium-Catalyzed Coupling of Aryl Halides and Amines -A Personal Account
    • Buchwald, S. L.; Mauger, C.; Mignani, G.; Scholz, U. Industrial-Scale Palladium-Catalyzed Coupling of Aryl Halides and Amines -A Personal Account. Adv. Synth. Catal., 2006, 348, 23.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 23
    • Buchwald, S.L.1    Mauger, C.2    Mignani, G.3    Scholz, U.4
  • 61
    • 33745395707 scopus 로고    scopus 로고
    • Discovery and Understanding of Transition-Metal-Catalyzed Aromatic Substitution Reactions
    • Hartwig, J. F. Discovery and Understanding of Transition-Metal-Catalyzed Aromatic Substitution Reactions. Synlett, 2006, 1283.
    • (2006) Synlett , pp. 1283
    • Hartwig, J.F.1
  • 62
    • 63349112681 scopus 로고    scopus 로고
    • Transition Metal-Catalysed, Direct and Site-Selective N1-, C2- or C3- Arylation of the Indole Nucleus: 20 Years of Improvements
    • Joucla, L.; Djakovitch, L. Transition Metal-Catalysed, Direct and Site-Selective N1-, C2- or C3- Arylation of the Indole Nucleus: 20 Years of Improvements. Adv. Synth. Catal., 2009, 351, 673.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 673
    • Joucla, L.1    Djakovitch, L.2
  • 64
    • 0001713836 scopus 로고
    • Some reactions of 3-halogenocinnolines catalysed by palladium compounds
    • Ames, D. E.; Bull, D. Some reactions of 3-halogenocinnolines catalysed by palladium compounds. Tetrahedron, 1982, 38, 383.
    • (1982) Tetrahedron , vol.38 , pp. 383
    • Ames, D.E.1    Bull, D.2
  • 65
    • 0000401303 scopus 로고    scopus 로고
    • Novel synthetic strategy of carbolines via palladium-catalyzed amination and arylation reaction
    • Iwaki, T.; Yasuhara, A.; Sakamoto, T. Novel synthetic strategy of carbolines via palladium-catalyzed amination and arylation reaction. J. Chem. Soc., Perkin Trans. 1, 1999, 1505.
    • (1999) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1505
    • Iwaki, T.1    Yasuhara, A.2    Sakamoto, T.3
  • 66
    • 0036406094 scopus 로고    scopus 로고
    • A novel catalytic one-pot synthesis of carbazoles via consecutive amination and C-H activation
    • Bedford, R. B.; Cazin, C. S. J. A novel catalytic one-pot synthesis of carbazoles via consecutive amination and C-H activation. Chem. Commun., 2002, 2310.
    • (2002) Chem. Commun , pp. 2310
    • Bedford, R.B.1    Cazin, C.S.J.2
  • 67
    • 12344290350 scopus 로고    scopus 로고
    • Synthesis of the benzo-β-carboline isoneocryptolepine: The missing indoloquinoline isomer in the alkaloid series cryptolepine, neocryptolepine and isocryptolepine
    • Hostyn, S.; Maes, B. U. W.; Pieters, L.; Lemiere, G. L. F.; Matyus, P.; Hajos, G.; Dommisse, R. A. Synthesis of the benzo-β-carboline isoneocryptolepine: the missing indoloquinoline isomer in the alkaloid series cryptolepine, neocryptolepine and isocryptolepine. Tetrahedron, 2005, 61, 1571.
    • (2005) Tetrahedron , vol.61 , pp. 1571
    • Hostyn, S.1    Maes, B.U.W.2    Pieters, L.3    Lemiere, G.L.F.4    Matyus, P.5    Hajos, G.6    Dommisse, R.A.7
  • 68
    • 0021303259 scopus 로고
    • Palladium Catalyzed Synthesis of Unsymmetrical Bithienyls from Thiopheneboronic acids and Halothiophenes
    • Gronowitz, S.; Bobosik, V.; Lawitz, K. Palladium Catalyzed Synthesis of Unsymmetrical Bithienyls from Thiopheneboronic acids and Halothiophenes. Chem. Scr., 1984, 23, 120.
    • (1984) Chem. Scr , vol.23 , pp. 120
    • Gronowitz, S.1    Bobosik, V.2    Lawitz, K.3
  • 69
    • 0000092204 scopus 로고
    • Palladium-Catalyzed Cross-Coupling Reactions of Organoboronic Acids with Organic Electrophiles
    • Martin, A. R.; Yang, Y. H. Palladium-Catalyzed Cross-Coupling Reactions of Organoboronic Acids with Organic Electrophiles. Acta Chem. Scand., 1993, 47, 221.
    • (1993) Acta Chem. Scand , vol.47 , pp. 221
    • Martin, A.R.1    Yang, Y.H.2
  • 70
    • 12344260184 scopus 로고
    • CVII.-Syntheses in the indole series. Part III. The theory of anhydronium base formation and the constitution of methosulphates, with some observations on the fluorescence of 5: 6-benz-4-carboline and its derivatives
    • Kermack, W. O.; Slater, R. H. CVII.-Syntheses in the indole series. Part III. The theory of anhydronium base formation and the constitution of methosulphates, with some observations on the fluorescence of 5: 6-benz-4-carboline and its derivatives. J. Chem. Soc., 1928, 789.
    • (1928) J. Chem. Soc , pp. 789
    • Kermack, W.O.1    Slater, R.H.2
  • 71
    • 32144431909 scopus 로고    scopus 로고
    • Palladium-Catalyzed Intramolecular N-Arylation of Heteroarenes: A Novel and Efficient Route to Benzimidazo[1,2-a]quinolines
    • Venkatesh, C.; Sundaram, G. S. M.; Ila, H.; Junjappa, H. Palladium-Catalyzed Intramolecular N-Arylation of Heteroarenes: A Novel and Efficient Route to Benzimidazo[1,2-a]quinolines. J. Org. Chem., 2006, 71, 1280.
    • (2006) J. Org. Chem , vol.71 , pp. 1280
    • Venkatesh, C.1    Sundaram, G.S.M.2    Ila, H.3    Junjappa, H.4
  • 72
    • 36448940133 scopus 로고    scopus 로고
    • Synthesis of benzo- γ-carboline alkaloid cryptosanginolentine by reaction of indole-2,3-dicarboxylic anhydrides with anilines
    • Miki, Y.; Kuromatsu, M.; Miyatake, H.; Hamamoto, H. Synthesis of benzo- γ-carboline alkaloid cryptosanginolentine by reaction of indole-2,3-dicarboxylic anhydrides with anilines. Tetrahedron Lett., 2007, 48, 9093.
    • (2007) Tetrahedron Lett , vol.48 , pp. 9093
    • Miki, Y.1    Kuromatsu, M.2    Miyatake, H.3    Hamamoto, H.4
  • 73
    • 22944483170 scopus 로고    scopus 로고
    • On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes
    • Tanaka, D.; Romeril, S. P.; Myers, A. G. On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes. J. Am. Chem. Soc., 2005, 127, 10323.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 10323
    • Tanaka, D.1    Romeril, S.P.2    Myers, A.G.3
  • 74
    • 1342327964 scopus 로고    scopus 로고
    • Heck-Type Arylation of 2-Cycloalken-1-ones with Arylpalladium Intermediates Formed by Decarboxylative Palladation and by Aryl Iodide Insertion
    • Tanaka, D.; Myers, A. G. Heck-Type Arylation of 2-Cycloalken-1-ones with Arylpalladium Intermediates Formed by Decarboxylative Palladation and by Aryl Iodide Insertion. Org. Lett., 2004, 6, 433.
    • (2004) Org. Lett , vol.6 , pp. 433
    • Tanaka, D.1    Myers, A.G.2
  • 75
    • 0037174448 scopus 로고    scopus 로고
    • Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates
    • Myers, A. G.; Tanaka, D.; Mannion, M. R. Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates. J. Am. Chem. Soc., 2002, 124, 11250.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 11250
    • Myers, A.G.1    Tanaka, D.2    Mannion, M.R.3
  • 76
    • 34248197452 scopus 로고    scopus 로고
    • Radical 6-endo-trig Cyclization of β, β-Difluoro-oisocyanostyrenes: A Facile Synthesis of 3-Fluoroquinolines and Their Application to the Synthesis of 11-Alkylated Cryptolepines
    • Mori, T.; Ichikawa, J. Radical 6-endo-trig Cyclization of β, β-Difluoro-oisocyanostyrenes: A Facile Synthesis of 3-Fluoroquinolines and Their Application to the Synthesis of 11-Alkylated Cryptolepines. Synlett, 2007, 1169.
    • (2007) Synlett , pp. 1169
    • Mori, T.1    Ichikawa, J.2
  • 77
    • 33845292599 scopus 로고    scopus 로고
    • The aza-Wittig reaction: An efficient tool for the construction of carbon-nitrogen double bonds
    • Palacios, F.; Alonso, C.; Aparicio, D.; Rubiales, G.; de los Santos, J. M. The aza-Wittig reaction: an efficient tool for the construction of carbon-nitrogen double bonds. Tetrahedron 2007, 63, 523.
    • (2007) Tetrahedron , vol.63 , pp. 523
    • Palacios, F.1    Alonso, C.2    Aparicio, D.3    Rubiales, G.4    de los Santos, J.M.5
  • 78
    • 0346970848 scopus 로고    scopus 로고
    • Application of Iminophosphorane-Based Methodologies for the Synthesis of Natural Products
    • Fresneda, P. M.; Molina, P. Application of Iminophosphorane-Based Methodologies for the Synthesis of Natural Products. Synlett, 2004, 1.
    • (2004) Synlett , pp. 1
    • Fresneda, P.M.1    Molina, P.2
  • 79
    • 0030756125 scopus 로고    scopus 로고
    • Formal Total Synthesis of the Alkaloid Cryptotackieine (Neocryptolepine)
    • Alajarin, M.; Molina, P.; Vidal, A. Formal Total Synthesis of the Alkaloid Cryptotackieine (Neocryptolepine). J. Nat. Prod., 1997, 60, 747.
    • (1997) J. Nat. Prod , vol.60 , pp. 747
    • Alajarin, M.1    Molina, P.2    Vidal, A.3
  • 80
    • 0033525049 scopus 로고    scopus 로고
    • Biradicals from Thermolysis of N-[2-(1-Alkynyl)phenyl]-N- phenylcarbodiimides and Their Subsequent Transformations to 6H-Indolo[2,3-b]quinolines
    • Shi, C.; Zhang, Q.; Wang, K. K. Biradicals from Thermolysis of N-[2-(1-Alkynyl)phenyl]-N- phenylcarbodiimides and Their Subsequent Transformations to 6H-Indolo[2,3-b]quinolines. J. Org. Chem., 1999, 64, 925.
    • (1999) J. Org. Chem , vol.64 , pp. 925
    • Shi, C.1    Zhang, Q.2    Wang, K.K.3
  • 81
    • 0032982021 scopus 로고    scopus 로고
    • Iminophosphorane-Mediated Synthesis of the Alkaloid Cryptotackieine
    • Molina, P.; Fresneda, P. M.; Delgado, S. Iminophosphorane-Mediated Synthesis of the Alkaloid Cryptotackieine. Synthesis, 1999, 326.
    • (1999) Synthesis , pp. 326
    • Molina, P.1    Fresneda, P.M.2    Delgado, S.3
  • 82
    • 0035898246 scopus 로고    scopus 로고
    • A novel approach to the indoloquinoline alkaloids cryptotackieine and cryptosanguinolentine by application of cyclization of o-vinylsubstituted arylheterocumulenes
    • Fresneda, P. M.; Molina, P.; Delgado, S. A novel approach to the indoloquinoline alkaloids cryptotackieine and cryptosanguinolentine by application of cyclization of o-vinylsubstituted arylheterocumulenes. Tetrahedron, 2001, 57, 6197.
    • (2001) Tetrahedron , vol.57 , pp. 6197
    • Fresneda, P.M.1    Molina, P.2    Delgado, S.3
  • 83
    • 58149170443 scopus 로고    scopus 로고
    • Application of the Pictet-Spengler reaction to aryl amine-based substrates having pyrimidine as a π-nucleophile: Synthesis of pyrimidoquinolines with structural analogy to benzonaphthyridines present in alkaloids
    • Agarwal, P. K.; Sharma, S. K.; Sawant, D.; Kundu, B. Application of the Pictet-Spengler reaction to aryl amine-based substrates having pyrimidine as a π-nucleophile: synthesis of pyrimidoquinolines with structural analogy to benzonaphthyridines present in alkaloids. Tetrahedron, 2009, 65, 1153.
    • (2009) Tetrahedron , vol.65 , pp. 1153
    • Agarwal, P.K.1    Sharma, S.K.2    Sawant, D.3    Kundu, B.4
  • 84
    • 0036944830 scopus 로고    scopus 로고
    • Synthesis of Cryptolepine and Cryptoteckieine from a Common Intermediate
    • Ho, T.-L.; Jou, D.-G. Synthesis of Cryptolepine and Cryptoteckieine from a Common Intermediate. Helv. Chim. Acta, 2002, 85, 3823.
    • (2002) Helv. Chim. Acta , vol.85 , pp. 3823
    • Ho, T.-L.1    Jou, D.-G.2
  • 85
    • 29744458599 scopus 로고    scopus 로고
    • Original and Rapid Access to New Alkaloid Analogues of Neocryptolepine: Synthesis of Substituted 6-Methyl-6H-indolo[2,3-b]quinolines via TDAE Strategy
    • Amiri-Attou, Q.; Terme, T.; Vanelle, P. Original and Rapid Access to New Alkaloid Analogues of Neocryptolepine: Synthesis of Substituted 6-Methyl-6H-indolo[2,3-b]quinolines via TDAE Strategy. Synlett, 2005, 3047.
    • (2005) Synlett , pp. 3047
    • Amiri-Attou, Q.1    Terme, T.2    Vanelle, P.3
  • 86
    • 0001548395 scopus 로고    scopus 로고
    • Nucleophilic Trifluoromethylation Using Trifluoromethyl Iodide. A New and Simple Alternative for the Trifluoromethylation of Aldehydes and Ketones
    • Ait-Mohand, S.; Takechi, N.; Medebielle, M.; Dolbier, W. R. Jr. Nucleophilic Trifluoromethylation Using Trifluoromethyl Iodide. A New and Simple Alternative for the Trifluoromethylation of Aldehydes and Ketones. Org. Lett., 2001, 3, 4271.
    • (2001) Org. Lett , vol.3 , pp. 4271
    • Ait-Mohand, S.1    Takechi, N.2    Medebielle, M.3    Dolbier Jr., W.R.4
  • 87
    • 0034992364 scopus 로고    scopus 로고
    • Tetrakis(dimethylamino) ethylene (TDAE) Mediated Addition of Heterocyclic Difluoromethyl Anions to Heteroaryl Aldehydes. A Facile Synthetic Method for New gem-Difluorinated Alcohols Derived from 4-Bromo-1-naphthylamine and 8-Quinolylamine
    • Medebielle, M.; Keirouz, R.; Okada, E.; Ashida, T. Tetrakis(dimethylamino) ethylene (TDAE) Mediated Addition of Heterocyclic Difluoromethyl Anions to Heteroaryl Aldehydes. A Facile Synthetic Method for New gem-Difluorinated Alcohols Derived from 4-Bromo-1-naphthylamine and 8-Quinolylamine. Synlett, 2001, 821.
    • (2001) Synlett , pp. 821
    • Medebielle, M.1    Keirouz, R.2    Okada, E.3    Ashida, T.4
  • 88
    • 34848868117 scopus 로고    scopus 로고
    • Double reductive cyclization: A facile synthesis of the indoloquinoline alkaloid cryptotackieine
    • Parvatkar, P. T.; Parameswaran, P. S.; Tilve, S. G. Double reductive cyclization: a facile synthesis of the indoloquinoline alkaloid cryptotackieine. Tetrahedron Lett., 2007, 48, 7870.
    • (2007) Tetrahedron Lett , vol.48 , pp. 7870
    • Parvatkar, P.T.1    Parameswaran, P.S.2    Tilve, S.G.3
  • 89
    • 54049155616 scopus 로고    scopus 로고
    • Unprecedented SnCl2·2H2O-mediated intramolecular cyclization of nitroarenes via C-N bond formation: A new entry to the synthesis of cryptotackieine and related skeletons
    • Sharma, S.; Kundu, B. Unprecedented SnCl2·2H2O-mediated intramolecular cyclization of nitroarenes via C-N bond formation: a new entry to the synthesis of cryptotackieine and related skeletons. Tetrahedron Lett., 2008, 49, 7062.
    • (2008) Tetrahedron Lett , vol.49 , pp. 7062
    • Sharma, S.1    Kundu, B.2
  • 90
    • 42549140767 scopus 로고    scopus 로고
    • Photochemical Reactions as Key Steps in Organic Synthesis
    • Hoffmann, N. Photochemical Reactions as Key Steps in Organic Synthesis. Chem. Rev., 2008, 108, 1052.
    • (2008) Chem. Rev , vol.108 , pp. 1052
    • Hoffmann, N.1
  • 91
    • 0037193143 scopus 로고    scopus 로고
    • A photochemical route to synthesize cryptosanguinolentine
    • Kumar, R. N.; Suresh, T.; Mohan, P. S. A photochemical route to synthesize cryptosanguinolentine. Tetrahedron Lett., 2002, 43, 3327.
    • (2002) Tetrahedron Lett , vol.43 , pp. 3327
    • Kumar, R.N.1    Suresh, T.2    Mohan, P.S.3
  • 92
    • 33646821395 scopus 로고    scopus 로고
    • Heteroatom directed photoannulation: Synthesis of indoloquinoline alkaloids: Cryptolepine, cryptotackieine, cryptosanguinolentine, and their methyl derivatives
    • Dhanabal, T.; Sangeetha, R.; Mohan, P. S. Heteroatom directed photoannulation: synthesis of indoloquinoline alkaloids: cryptolepine, cryptotackieine, cryptosanguinolentine, and their methyl derivatives. Tetrahedron, 2006, 62, 6258.
    • (2006) Tetrahedron , vol.62 , pp. 6258
    • Dhanabal, T.1    Sangeetha, R.2    Mohan, P.S.3
  • 93
    • 68149181518 scopus 로고    scopus 로고
    • Photo induced synthesis of methyl derivative of cryptosanguinolentine
    • Pitchai, P.; Mohan, P. S.; Gengan, R. M. Photo induced synthesis of methyl derivative of cryptosanguinolentine. Indian J. Chem., 2009, 48B, 692.
    • (2009) Indian J. Chem , vol.48 B , pp. 692
    • Pitchai, P.1    Mohan, P.S.2    Gengan, R.M.3
  • 94
    • 85067364234 scopus 로고
    • A Convenient Synthesis of 3-Halo-4-oxo-1,4- dihydroquinolines (3-Halo-4-hydroxyquinolines)
    • Renault, J.; Mlliet, P.; Reanault, S.; Berlot, J. A Convenient Synthesis of 3-Halo-4-oxo-1,4- dihydroquinolines (3-Halo-4-hydroxyquinolines). Synthesis, 1977, 865.
    • (1977) Synthesis , pp. 865
    • Renault, J.1    Mlliet, P.2    Reanault, S.3    Berlot, J.4
  • 99
  • 100
    • 0029994789 scopus 로고    scopus 로고
    • Indole-β-nucleophilic substitution. Part 9 nitrogen nucleophiles. Syntheses of hydroxycryptolepine, cryptolepine, and quindoline
    • Cooper, M. M.; Lovell, J. M.; Joule, J. A. Indole-β-nucleophilic substitution. Part 9 nitrogen nucleophiles. Syntheses of hydroxycryptolepine, cryptolepine, and quindoline. Tetrahedron Lett., 1996, 37, 4283.
    • (1996) Tetrahedron Lett , vol.37 , pp. 4283
    • Cooper, M.M.1    Lovell, J.M.2    Joule, J.A.3
  • 102
    • 24344509099 scopus 로고
    • Carbazoles, carbolines, and related compounds. I Quindoline derivatives
    • Holt, J. S.; Petrow, V. Carbazoles, carbolines, and related compounds. I Quindoline derivatives. J. Chem. Soc., 1947, 607.
    • (1947) J. Chem. Soc , pp. 607
    • Holt, J.S.1    Petrow, V.2
  • 103
    • 33847479495 scopus 로고
    • Alkylation of quindoline and 11-quindolinecarboxylic acid
    • Chem. Abstr. no. 107: 39658y
    • Degutis, J.; Ezerskaite, A. Alkylation of quindoline and 11-quindolinecarboxylic acid. Khim. Geterotsikl. Soedin., 1986, 1375 (Chem. Abstr. no. 107: 39658y).
    • (1986) Khim. Geterotsikl. Soedin , pp. 1375
    • Degutis, J.1    Ezerskaite, A.2
  • 106
    • 0033786416 scopus 로고    scopus 로고
    • A New Approach to the Synthesis of Benzofuro[3,2- b]quinolines, Benzothieno[3,2-b]quinolines and Indolo[3,2- b]quinolines
    • Radl, S.; Konvicka, P.; Vachal, P. A New Approach to the Synthesis of Benzofuro[3,2- b]quinolines, Benzothieno[3,2-b]quinolines and Indolo[3,2- b]quinolines. J. Heterocycl. Chem., 2000, 37, 855.
    • (2000) J. Heterocycl. Chem , vol.37 , pp. 855
    • Radl, S.1    Konvicka, P.2    Vachal, P.3
  • 107
    • 0002174959 scopus 로고
    • Some Examples of Aromatic Nucleophilic Denitrocyclization Reactions
    • Radl, S. Some Examples of Aromatic Nucleophilic Denitrocyclization Reactions. Janssen Chim. Acta., 1993, 11, 12.
    • (1993) Janssen Chim. Acta , vol.11 , pp. 12
    • Radl, S.1
  • 108
    • 4644277659 scopus 로고    scopus 로고
    • An improved synthesis of neocryptolepine
    • Engqvist, R.; Bergman, J. An improved synthesis of neocryptolepine. Org. Prep. Proced. Int., 2004, 36, 386.
    • (2004) Org. Prep. Proced. Int , vol.36 , pp. 386
    • Engqvist, R.1    Bergman, J.2
  • 109
    • 4043125913 scopus 로고    scopus 로고
    • A Concise Formal Synthesis of Alkaloid Cryptotackiene and Substituted 6H-Indolo[2,3-b]quinolines
    • Sundaram, G. S. M.; Venkatesh, C.; Syam Kumar, U. K.; Ila, H.; Junjappa, H. A Concise Formal Synthesis of Alkaloid Cryptotackiene and Substituted 6H-Indolo[2,3-b]quinolines. J. Org. Chem., 2004, 69, 5760.
    • (2004) J. Org. Chem , vol.69 , pp. 5760
    • Sundaram, G.S.M.1    Venkatesh, C.2    Syam, K.U.K.3    Ila, H.4    Junjappa, H.5
  • 110
    • 19544365549 scopus 로고    scopus 로고
    • Fischer indole synthesis of the indoloquinoline alkaloid: Cryptosanguinolentine
    • Dhanabal, T.; Sangeetha, R.; Mohan, P. S. Fischer indole synthesis of the indoloquinoline alkaloid: cryptosanguinolentine. Tetrahedron Lett., 2005, 46, 4509.
    • (2005) Tetrahedron Lett , vol.46 , pp. 4509
    • Dhanabal, T.1    Sangeetha, R.2    Mohan, P.S.3
  • 111
    • 28844449160 scopus 로고    scopus 로고
    • Thermal cyclization of 3-arylamino-3-(2-nitrophenyl)-propenal Schiff base hydrochlorides followed by triethyl phosphite mediated deoxygenation: A facile synthesis of quindolines
    • Dutta, B.; Some, S.; Ray, J. K. Thermal cyclization of 3-arylamino-3-(2-nitrophenyl)-propenal Schiff base hydrochlorides followed by triethyl phosphite mediated deoxygenation: a facile synthesis of quindolines. Tetrahedron Lett., 2006, 47, 377.
    • (2006) Tetrahedron Lett , vol.47 , pp. 377
    • Dutta, B.1    Some, S.2    Ray, J.K.3
  • 112
    • 48249156559 scopus 로고    scopus 로고
    • Microwave-Assisted Syntheses of N-Heterocycles Using Alkenone-, Alkynone- and Aryl-carbonyl O-Phenyl Oximes: Formal Synthesis of Neocryptolepine
    • Portela-Cubillo, F.; Scott, J. S.; Walton, J. C. Microwave-Assisted Syntheses of N-Heterocycles Using Alkenone-, Alkynone- and Aryl-carbonyl O-Phenyl Oximes: Formal Synthesis of Neocryptolepine. J. Org. Chem., 2008, 73, 5558.
    • (2008) J. Org. Chem , vol.73 , pp. 5558
    • Portela-Cubillo, F.1    Scott, J.S.2    Walton, J.C.3
  • 113
    • 0037429056 scopus 로고    scopus 로고
    • Studies of the reactions between indole- 2,3-diones (isatins) and 2-aminobenzylamine
    • Bergman, J.; Engqvist, R.; Stalhandske, C.; Wallberg, H. Studies of the reactions between indole- 2,3-diones (isatins) and 2-aminobenzylamine. Tetrahedron, 2003, 59, 1033.
    • (2003) Tetrahedron , vol.59 , pp. 1033
    • Bergman, J.1    Engqvist, R.2    Stalhandske, C.3    Wallberg, H.4
  • 114
    • 70350707658 scopus 로고    scopus 로고
    • An Expeditious I2- Catalyzed Entry into 6H- Indolo[2,3-b]quinoline System of Cryptotackieine
    • Parvatkar, P. T.; Parameswaran, P. S.; Tilve, S. G. An Expeditious I2- Catalyzed Entry into 6H- Indolo[2,3-b]quinoline System of Cryptotackieine. J. Org. Chem., 2009, 74, 8369.
    • (2009) J. Org. Chem , vol.74 , pp. 8369
    • Parvatkar, P.T.1    Parameswaran, P.S.2    Tilve, S.G.3
  • 115
    • 77953962789 scopus 로고    scopus 로고
    • A direct synthesis of neocryptolepine and isocryptolepine
    • Kraus, G. A.; Guo, H. A direct synthesis of neocryptolepine and isocryptolepine. Tetrahedron Lett., 2010, 51, 4137.
    • (2010) Tetrahedron Lett , vol.51 , pp. 4137
    • Kraus, G.A.1    Guo, H.2
  • 116
    • 33744748302 scopus 로고    scopus 로고
    • Biomimetic Approach to Perophoramidine and Communesin via an Intramolecular Cyclopropanation Reaction
    • Yang, J.; Song, H.; Xiao, X.; Wang, J.; Qin, Y. Biomimetic Approach to Perophoramidine and Communesin via an Intramolecular Cyclopropanation Reaction. Org. Lett., 2006, 8, 2187.
    • (2006) Org. Lett , vol.8 , pp. 2187
    • Yang, J.1    Song, H.2    Xiao, X.3    Wang, J.4    Qin, Y.5


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