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Volumn , Issue , 2011, Pages 221-265

Indoles and Indolizidines

Author keywords

Alkaloids; Heterocycles; Indoles; Indolines; Indolizidines; Natural products; Oxindoles; Synthesis

Indexed keywords


EID: 79958801564     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527634880.ch7     Document Type: Chapter
Times cited : (57)

References (230)
  • 2
    • 84977496150 scopus 로고
    • Ueber das Morphium, eine neue salzfähige Grundlage, und die Mekonsäure, als Hauptbestandtheile des Opiums
    • Sertürner, F.W. (1817) Ueber das Morphium, eine neue salzfähige Grundlage, und die Mekonsäure, als Hauptbestandtheile des Opiums. Ann. Der Physik (Berlin), 55 (1), 56-90
    • (1817) Ann. Der Physik (Berlin) , vol.55 , Issue.1 , pp. 56-90
    • Sertürner, F.W.1
  • 3
    • 0024539982 scopus 로고
    • Schmerz-und Betäubungsmittel vor 1600 Ein fast unbekanntes Kapitel der Arzneimittelgeschichte
    • Schmitz, R. and Kuhlen, F.-J. (1989) Schmerz-und Betäubungsmittel vor 1600. Ein fast unbekanntes Kapitel der Arzneimittelgeschichte. Pharm. Unserer Zeit, 18 (1), 11-19
    • (1989) Pharm. Unserer Zeit , vol.18 , Issue.1 , pp. 11-19
    • Schmitz, R.1    Kuhlen, F.-J.2
  • 4
    • 2342579565 scopus 로고    scopus 로고
    • The isolation of morphine-first principles in science and ethics
    • Huxtable, R.J. and Schwartz, S.K.W. (2001) The isolation of morphine-first principles in science and ethics. Mol. Interv., 1 (4), 189-191.
    • (2001) Mol. Interv. , vol.1 , Issue.4 , pp. 189-191
    • Huxtable, R.J.1    Schwartz, S.K.W.2
  • 5
    • 85172021577 scopus 로고
    • Versuche zur Synthese des Coniin
    • Ladenburg, A. (1886) Versuche zur Synthese des Coniin. Ber. Dtsch. Chem. Ges., 19 (1), 439-441.
    • (1886) Ber. Dtsch. Chem. Ges. , vol.19 , Issue.1 , pp. 439-441
    • Ladenburg, A.1
  • 6
    • 84883902953 scopus 로고    scopus 로고
    • MDL Information Systems Inc., MDL Drug Data Report. MDL Information Systems Inc., San Leandro, CA
    • MDL Information Systems Inc., MDL Drug Data Report. MDL Information Systems Inc., San Leandro, CA.
  • 11
    • 11144349848 scopus 로고    scopus 로고
    • Alkaloids from amphibian skin
    • 1st edn (ed. S.W. Pelletier), Pergamon, New York, USA
    • Daly, J.W., Garraffo, H.M. and Spande, T.F. (1999) Alkaloids from amphibian skin, in Alkaloids: Chemical and Biological Perspectives, vol. 13, 1st edn (ed. S.W. Pelletier), Pergamon, New York, USA, pp. 1-161.
    • (1999) Alkaloids: Chemical and Biological Perspectives , vol.13 , pp. 1-161
    • Daly, J.W.1    Garraffo, H.M.2    Spande, T.F.3
  • 12
    • 27844526992 scopus 로고    scopus 로고
    • Alkaloids from amphibian skin: a tabulation of over eight-hundred compounds
    • Daly, J.W., Spande, T.F. and Garraffo, H.M. (2005) Alkaloids from amphibian skin: a tabulation of over eight-hundred compounds. J. Nat. Prod., 68 (10), 1556-1575.
    • (2005) J. Nat. Prod. , vol.68 , Issue.10 , pp. 1556-1575
    • Daly, J.W.1    Spande, T.F.2    Garraffo, H.M.3
  • 13
    • 0037366605 scopus 로고    scopus 로고
    • The combinatorial synthesis of bicyclic privileged structures or privileged substructures
    • Horton, D.A., Bourne, G.T. and Smyth, M.L. (2003) The combinatorial synthesis of bicyclic privileged structures or privileged substructures. Chem. Rev., 103 (3), 893-930
    • (2003) Chem. Rev. , vol.103 , Issue.3 , pp. 893-930
    • Horton, D.A.1    Bourne, G.T.2    Smyth, M.L.3
  • 15
    • 0002979399 scopus 로고    scopus 로고
    • The art and science of total synthesis at the dawn of the twenty-first century
    • Nicolaou, K.C., Vourloumis, D., Winssinger, N. and Baran, P.S. (2000) The art and science of total synthesis at the dawn of the twenty-first century. Angew. Chem. Int. Ed., 39 (1), 44-122.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , Issue.1 , pp. 44-122
    • Nicolaou, K.C.1    Vourloumis, D.2    Winssinger, N.3    Baran, P.S.4
  • 20
    • 0242323632 scopus 로고    scopus 로고
    • A concise and flexible total synthesis of (-)-diazonamide A
    • Burgett, A.W.G., Li, Q., Wei, Q. and Harran, P.G. (2003) A concise and flexible total synthesis of (-)-diazonamide A. Angew. Chem. Int. Ed., 42 (40), 4961-4966
    • (2003) Angew. Chem. Int. Ed. , vol.42 , Issue.40 , pp. 4961-4966
    • Burgett, A.W.G.1    Li, Q.2    Wei, Q.3    Harran, P.G.4
  • 21
    • 0035905352 scopus 로고    scopus 로고
    • Total synthesis of nominal diazonamides-part: 1convergent preparation of the structure proposed for (-)-diazonamide A
    • Li, J., Jeong, S., Esser, L. and Harran, P.G. (2001) Total synthesis of nominal diazonamides-part 1: convergent preparation of the structure proposed for (-)-diazonamide A. Angew. Chem. Int. Ed., 40 (24), 4765-4769
    • (2001) Angew. Chem. Int. Ed. , vol.40 , Issue.24 , pp. 4765-4769
    • Li, J.1    Jeong, S.2    Esser, L.3    Harran, P.G.4
  • 22
    • 0035905532 scopus 로고    scopus 로고
    • Total synthesis of nominal diazonamides-part: 2 on the true structure and origin of natural isolates
    • Li, J., Burgett, A.W.G., Esser, L., Amezcua, C. and Harran, P.G. (2001) Total synthesis of nominal diazonamides-part 2: on the true structure and origin of natural isolates. Angew. Chem. Int. Ed., 40 (24), 4770-4773.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , Issue.24 , pp. 4770-4773
    • Li, J.1    Burgett, A.W.G.2    Esser, L.3    Amezcua, C.4    Harran, P.G.5
  • 26
    • 0037036807 scopus 로고    scopus 로고
    • Enantioselective total synthesis of quadrigemine C and psycholeine
    • Lebsack, A.D., Link, J.T., Overman, L.E. and Stearns, B.A. (2002) Enantioselective total synthesis of quadrigemine C and psycholeine. J. Am. Chem. Soc., 124 (31), 9008-9009.
    • (2002) J. Am. Chem. Soc. , vol.124 , Issue.31 , pp. 9008-9009
    • Lebsack, A.D.1    Link, J.T.2    Overman, L.E.3    Stearns, B.A.4
  • 27
    • 0033591940 scopus 로고    scopus 로고
    • Enantioselective total synthesis of aspidophytine
    • He, F., Bo, Y., Altom, J.D. and Corey, E.J. (1999) Enantioselective total synthesis of aspidophytine. J. Am. Chem. Soc., 121 (28), 6771-6772.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.28 , pp. 6771-6772
    • He, F.1    Bo, Y.2    Altom, J.D.3    Corey, E.J.4
  • 28
    • 0038296199 scopus 로고    scopus 로고
    • Short, enantioselective total synthesis of okaramine N
    • Baran, P.S., Guerrero, C.A. and Corey, E.J. (2003) Short, enantioselective total synthesis of okaramine N. J. Am. Chem. Soc., 125 (19), 5628-5629.
    • (2003) J. Am. Chem. Soc. , vol.125 , Issue.19 , pp. 5628-5629
    • Baran, P.S.1    Guerrero, C.A.2    Corey, E.J.3
  • 29
    • 0025290810 scopus 로고
    • The total synthesis of dl-indolizomycin
    • Kim, G., Chu-Moyer, M.Y. and Danishefsky, S.J. (1990) The total synthesis of dl-indolizomycin. J. Am. Chem. Soc., 112 (5), 2003-2005
    • (1990) J. Am. Chem. Soc. , vol.112 , Issue.5 , pp. 2003-2005
    • Kim, G.1    Chu-Moyer, M.Y.2    Danishefsky, S.J.3
  • 31
    • 13244268408 scopus 로고    scopus 로고
    • Actinophyllic acid, a potent indole alkaloid inhibitor of the coupled enzyme assay carboxypeptidase U/hippuricase from the leaves of Alstonia actinophylla (apocynaceae)
    • Carroll, A.R., Hyde, E., Smith, J., Quinn, R.J., Guymer, G. and Forster, P.I. (2005) Actinophyllic acid, a potent indole alkaloid inhibitor of the coupled enzyme assay carboxypeptidase U/hippuricase from the leaves of Alstonia actinophylla (apocynaceae). J. Org. Chem., 70 (3), 1096-1099.
    • (2005) J. Org. Chem. , vol.70 , Issue.3 , pp. 1096-1099
    • Carroll, A.R.1    Hyde, E.2    Smith, J.3    Quinn, R.J.4    Guymer, G.5    Forster, P.I.6
  • 32
    • 45249090324 scopus 로고    scopus 로고
    • Total synthesis of (±)-actinophyllic acid
    • Martin, C.L., Overman, L.E. and Rohde, J.M. (2008) Total synthesis of (±)-actinophyllic acid. J. Am. Chem. Soc., 130 (24), 7568-7569
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.24 , pp. 7568-7569
    • Martin, C.L.1    Overman, L.E.2    Rohde, J.M.3
  • 33
    • 65249108138 scopus 로고    scopus 로고
    • Absolute configuration of actinophyllic acid as determined through chiroptical data
    • Taniguchi, T., Martin, C.L., Monde, K., Nakanishi, K., Berova, N. and Overman, L.E. (2009) Absolute configuration of actinophyllic acid as determined through chiroptical data. J. Nat. Prod., 72 (3), 430-432.
    • (2009) J. Nat. Prod. , vol.72 , Issue.3 , pp. 430-432
    • Taniguchi, T.1    Martin, C.L.2    Monde, K.3    Nakanishi, K.4    Berova, N.5    Overman, L.E.6
  • 34
    • 0034595978 scopus 로고    scopus 로고
    • Dragmacidin F: a new antiviral bromoindole alkaloid from the Mediterranean sponge Halicortex sp
    • Cutignano, A., Bifulco, G., Bruno, I., Casapullo, A., Gomez-Paloma, L. and Riccio, R. (2000) Dragmacidin F: a new antiviral bromoindole alkaloid from the Mediterranean sponge Halicortex sp. Tetrahedron, 56 (23), 3743-3748.
    • (2000) Tetrahedron , vol.56 , Issue.23 , pp. 3743-3748
    • Cutignano, A.1    Bifulco, G.2    Bruno, I.3    Casapullo, A.4    Gomez-Paloma, L.5    Riccio, R.6
  • 35
    • 3543120754 scopus 로고    scopus 로고
    • The total synthesis of (+)-dragmacidin F
    • Garg, N.K., Caspi, D.D. and Stoltz, B.M. (2004) The total synthesis of (+)-dragmacidin F. J. Am. Chem. Soc., 126 (31), 9552-9553
    • (2004) J. Am. Chem. Soc. , vol.126 , Issue.31 , pp. 9552-9553
    • Garg, N.K.1    Caspi, D.D.2    Stoltz, B.M.3
  • 36
    • 17744378379 scopus 로고    scopus 로고
    • Development of an enantiodivergent strategy for the total synthesis of (+)-and (-)-dragmacidin F from a single enantiomer of quinic acid
    • Garg, N.K., Caspi, D.D. and Stoltz, B.M. (2005) Development of an enantiodivergent strategy for the total synthesis of (+)-and (-)-dragmacidin F from a single enantiomer of quinic acid. J. Am. Chem. Soc., 127 (16), 5970-5978.
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.16 , pp. 5970-5978
    • Garg, N.K.1    Caspi, D.D.2    Stoltz, B.M.3
  • 37
    • 0014403903 scopus 로고
    • Tremorgenic toxin from Penicillium cyclopium grown on food materials
    • Wilson, B.J., Wilson, C.H. and Hayes, A.W. (1968) Tremorgenic toxin from Penicillium cyclopium grown on food materials. N ature, 220 (5162), 77-78.
    • (1968) N ature , vol.220 , Issue.5162 , pp. 77-78
    • Wilson, B.J.1    Wilson, C.H.2    Hayes, A.W.3
  • 40
    • 0027973653 scopus 로고
    • Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata Relationship to fischerindoles and hapalinodoles
    • Stratmann, K., Moore, R.E., Bonjouklian, R., Deeter, J.B., Patterson, G.M.L., Shaffer, S., Smith, C.D. and Smitka, T.A. (1994) Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata. Relationship to fischerindoles and hapalinodoles. J. Am. Chem. Soc., 116 (22), 9935-9942.
    • (1994) J. Am. Chem. Soc. , vol.116 , Issue.22 , pp. 9935-9942
    • Stratmann, K.1    Moore, R.E.2    Bonjouklian, R.3    Deeter, J.B.4    Patterson, G.M.L.5    Shaffer, S.6    Smith, C.D.7    Smitka, T.A.8
  • 41
    • 27644566322 scopus 로고    scopus 로고
    • Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G
    • Baran, P.S. and Richter, J.M. (2005) Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G. J. Am. Chem. Soc., 127 (44), 15394-15396
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.44 , pp. 15394-15396
    • Baran, P.S.1    Richter, J.M.2
  • 42
    • 33947602410 scopus 로고    scopus 로고
    • Total synthesis of marine natural products without using protecting groups
    • Baran, P.S., Maimone, T.J. and Richter, J.M. (2007) Total synthesis of marine natural products without using protecting groups. Nature, 446 (7134), 404-408
    • (2007) Nature , vol.446 , Issue.7134 , pp. 404-408
    • Baran, P.S.1    Maimone, T.J.2    Richter, J.M.3
  • 43
    • 58849128316 scopus 로고    scopus 로고
    • Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach
    • Richter, J.M., Ishihara, Y., Masuda, T., Whitefield, B.W., Llamas, T., Pohjakallio, A. and Baran, P.S. (2008) Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach. J. Am. Chem. Soc., 130 (52), 17938-17954.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.52 , pp. 17938-17954
    • Richter, J.M.1    Ishihara, Y.2    Masuda, T.3    Whitefield, B.W.4    Llamas, T.5    Pohjakallio, A.6    Baran, P.S.7
  • 46
    • 0344299039 scopus 로고    scopus 로고
    • New cytotoxic epidithiodioxopiperazines related to verticillin A from a marine isolate of the fungus Penicillium
    • Son, B.W., Jensen, P.R., Kauffman, C.A. and Fenical, W. (1999) New cytotoxic epidithiodioxopiperazines related to verticillin A from a marine isolate of the fungus Penicillium. Nat. Prod. Lett., 13 (3), 213-222.
    • (1999) Nat. Prod. Lett. , vol.13 , Issue.3 , pp. 213-222
    • Son, B.W.1    Jensen, P.R.2    Kauffman, C.A.3    Fenical, W.4
  • 47
    • 64849113664 scopus 로고    scopus 로고
    • Total synthesis of (+)-11,11'-dideoxyverticillin A
    • Kim, J., Ashenhurst, J.A. and Movassaghi, M. (2009) Total synthesis of (+)-11,11'-dideoxyverticillin A. Science, 324 (5924), 238-241.
    • (2009) Science , vol.324 , Issue.5924 , pp. 238-241
    • Kim, J.1    Ashenhurst, J.A.2    Movassaghi, M.3
  • 48
    • 0005033403 scopus 로고
    • Normavacurine and minfiensine, two new alkaloids with C 19 H 22 N 2 O formula from Strychnos species
    • Massiot, G., Thépenier, P., Jacquier, M.-J., Le Men-Olivier, L. and Delaude, C. (1989) Normavacurine and minfiensine, two new alkaloids with C 19 H 22 N 2 O formula from Strychnos species. Heterocycles, 29 (8), 1435-1438.
    • (1989) Heterocycles , vol.29 , Issue.8 , pp. 1435-1438
    • Massiot, G.1    Thépenier, P.2    Jacquier, M.-J.3    Le Men-Olivier, L.4    Delaude, C.5
  • 49
    • 22944450392 scopus 로고    scopus 로고
    • Sequential catalytic asymmetric Heck - iminium ion cyclization: enantioselective total synthesis of the Strychnos alkaloid minfiensine
    • Dounay, A.B., Overman, L.E. and Wrobleski, A.D. (2005) Sequential catalytic asymmetric Heck - iminium ion cyclization: enantioselective total synthesis of the Strychnos alkaloid minfiensine. J. Am. Chem. Soc., 127 (29), 10186-10187.
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.29 , pp. 10186-10187
    • Dounay, A.B.1    Overman, L.E.2    Wrobleski, A.D.3
  • 50
    • 42149168996 scopus 로고    scopus 로고
    • Total synthesis of the Strychnos alkaloid (+)-minfiensine: Tandem enantioselective intramolecular Heck - iminium ion cyclization
    • Dounay, A.B., Humphreys, P.G., Overman, L.E. and Wrobleski, A.D. (2008) Total synthesis of the Strychnos alkaloid (+)-minfiensine: Tandem enantioselective intramolecular Heck - iminium ion cyclization. J. Am. Chem. Soc., 130 (15), 5368-5377.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.15 , pp. 5368-5377
    • Dounay, A.B.1    Humphreys, P.G.2    Overman, L.E.3    Wrobleski, A.D.4
  • 51
    • 44049105075 scopus 로고    scopus 로고
    • Efficient assembly of an indole alkaloid skeleton by cyclopropanation: concise total synthesis of (±)-minfiensine
    • Shen, L., Zhang, M., Wu, Y. and Qin, Y. (2008) Efficient assembly of an indole alkaloid skeleton by cyclopropanation: concise total synthesis of (±)-minfiensine. Angew. Chem. Int. Ed., 47 (19), 3618-3621.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , Issue.19 , pp. 3618-3621
    • Shen, L.1    Zhang, M.2    Wu, Y.3    Qin, Y.4
  • 52
    • 70349753180 scopus 로고    scopus 로고
    • Nine-step enantioselective total synthesis of (+)-minfiensine
    • Jones, S.B., Simmons, B. and MacMillan, D.W.C. (2009) Nine-step enantioselective total synthesis of (+)-minfiensine. J. Am. Chem. Soc., 131 (38), 13606-13607.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.38 , pp. 13606-13607
    • Jones, S.B.1    Simmons, B.2    MacMillan, D.W.C.3
  • 53
    • 84955867829 scopus 로고
    • Alkaloide aus Diplorrhynchus condylocarpon (MUELL ARG. ) Pichon ssp. mossambicensis (BENTH. ) Duvign
    • Stauffacher, D. (1961) Alkaloide aus Diplorrhynchus condylocarpon (MUELL. ARG.) Pichon ssp. mossambicensis (BENTH.) Duvign. Helv. Chim. Acta, 44 (7), 2006-2015.
    • (1961) Helv. Chim. Acta , vol.44 , Issue.7 , pp. 2006-2015
    • Stauffacher, D.1
  • 56
    • 67749133710 scopus 로고    scopus 로고
    • Efficient access to the core of the Strychnos Aspidosperma and Iboga alkaloids. A short synthesis of norfluorocurarine
    • Martin, D.B.C. and Vanderwal, C.D. (2009) Efficient access to the core of the Strychnos, Aspidosperma and Iboga alkaloids. A short synthesis of norfluorocurarine. J. Am. Chem. Soc., 131 (10), 3472-3473.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.10 , pp. 3472-3473
    • Martin, D.B.C.1    Vanderwal, C.D.2
  • 57
    • 4444256771 scopus 로고    scopus 로고
    • New type of trimeric and pentameric indole alkaloids from Psychotria rostrata
    • Takayama, H., Mori, I., Kitajima, M., Aimi, N. and Lajis, N.H. (2004) New type of trimeric and pentameric indole alkaloids from Psychotria rostrata. Org. Lett., 6 (17), 2945-2948.
    • (2004) Org. Lett. , vol.6 , Issue.17 , pp. 2945-2948
    • Takayama, H.1    Mori, I.2    Kitajima, M.3    Aimi, N.4    Lajis, N.H.5
  • 58
    • 50249176473 scopus 로고    scopus 로고
    • Total synthesis of (±)-psychotrimine
    • Newhouse, T. and Baran, P.S. (2008) Total synthesis of (±)-psychotrimine. J. Am. Chem. Soc., 130 (33), 10886-10887.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.33 , pp. 10886-10887
    • Newhouse, T.1    Baran, P.S.2
  • 59
    • 84973253942 scopus 로고
    • New alkaloids from ants: identification and synthesis of (3 R,5 S,9 R)-3-butyl-5-(1-oxopropyl) indolizidine and (3 R,5 R,9 R)-3-butyl-5-(1 -oxopropyl)indolizidine, constituents of the poison gland secretion in Myrmicaria eumenoides (hymenoptera, formicidae)
    • Francke, W., Schröder, F., Walter, F., Sinnwell, V., Baumann, H. and Kaib, M. (1995) New alkaloids from ants: identification and synthesis of (3 R,5 S,9 R)-3-butyl-5-(1-oxopropyl) indolizidine and (3 R,5 R,9 R)-3-butyl-5-(1 -oxopropyl)indolizidine, constituents of the poison gland secretion in Myrmicaria eumenoides (hymenoptera, formicidae). Liebigs Ann., (6), 965-977
    • (1995) Liebigs Ann , Issue.6 , pp. 965-977
    • Francke, W.1    Schröder, F.2    Walter, F.3    Sinnwell, V.4    Baumann, H.5    Kaib, M.6
  • 61
    • 0029775596 scopus 로고    scopus 로고
    • Myrmicarin 430A: a new heptacyclic alkaloid from Myrmicaria ants
    • Schröder, F., Sinnwell, V., Baumann, H. and Kaib, M. (1996) Myrmicarin 430A: a new heptacyclic alkaloid from Myrmicaria ants. Chem. Commun., (18), 2139-2140
    • (1996) Chem. Commun. , Issue.18 , pp. 2139-2140
    • Schröder, F.1    Sinnwell, V.2    Baumann, H.3    Kaib, M.4
  • 63
    • 26444462446 scopus 로고    scopus 로고
    • Enantioselective total synthesis of tricyclic myrmicarin alkaloids
    • Movassaghi, M. and Ondrus, A.E. (2005) Enantioselective total synthesis of tricyclic myrmicarin alkaloids. Org. Lett., 7 (20), 4423-4426.
    • (2005) Org. Lett. , vol.7 , Issue.20 , pp. 4423-4426
    • Movassaghi, M.1    Ondrus, A.E.2
  • 64
    • 0034703296 scopus 로고    scopus 로고
    • Serratezomines A - C, new alkaloids from Lycopodium serratum var. serratum
    • Morita, H., Arisaka, M., Yoshida, N. and Kobayashi, J. (2000) Serratezomines A - C, new alkaloids from Lycopodium serratum var. serratum. J. Org. Chem., 65 (19), 6241-6245.
    • (2000) J. Org. Chem. , vol.65 , Issue.19 , pp. 6241-6245
    • Morita, H.1    Arisaka, M.2    Yoshida, N.3    Kobayashi, J.4
  • 65
    • 70249116098 scopus 로고    scopus 로고
    • Total synthesis of the Lycopodium alkaloid (+)-serratezomine A
    • Chandra, A., Pigza, J.A., Han, J.-S., Mutnick, D. and Johnston, J.N. (2009) Total synthesis of the Lycopodium alkaloid (+)-serratezomine A. J. Am. Chem. Soc., 131 (10), 3470-3471.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.10 , pp. 3470-3471
    • Chandra, A.1    Pigza, J.A.2    Han, J.-S.3    Mutnick, D.4    Johnston, J.N.5
  • 66
    • 24944454291 scopus 로고    scopus 로고
    • Carboxypeptidase U (TAFIa): a metallocarboxypeptidase with a distinct role in haemostasis and a possible risk factor for thrombotic disease
    • Leurs, J. and Hendriks, D. (2005) Carboxypeptidase U (TAFIa): a metallocarboxypeptidase with a distinct role in haemostasis and a possible risk factor for thrombotic disease. Thromb. Haemost., 94 (3), 471-487.
    • (2005) Thromb. Haemost. , vol.94 , Issue.3 , pp. 471-487
    • Leurs, J.1    Hendriks, D.2
  • 67
    • 70349932331 scopus 로고    scopus 로고
    • Progress toward the total synthesis of (±)-actinophyllic acid
    • Vaswani, R.G., Day, J.J. and Wood, J.L. (2009) Progress toward the total synthesis of (±)-actinophyllic acid. Org. Lett., 11 (20), 4532-4535.
    • (2009) Org. Lett. , vol.11 , Issue.20 , pp. 4532-4535
    • Vaswani, R.G.1    Day, J.J.2    Wood, J.L.3
  • 68
    • 0001626504 scopus 로고
    • Charge as a key component in reaction design The invention of cationic cyclization reactions of importance in synthesis
    • Overman, L.E. (1992) Charge as a key component in reaction design. The invention of cationic cyclization reactions of importance in synthesis. Acc. Chem. Res., 25 (8), 352-359
    • (1992) Acc. Chem. Res. , vol.25 , Issue.8 , pp. 352-359
    • Overman, L.E.1
  • 69
    • 2942574530 scopus 로고    scopus 로고
    • Chiral heterocycles by iminium ion cyclization
    • Royer, J., Bonin, M. and Micouin, L. (2004) Chiral heterocycles by iminium ion cyclization. Chem. Rev., 104 (5), 2311-2352.
    • (2004) Chem. Rev. , vol.104 , Issue.5 , pp. 2311-2352
    • Royer, J.1    Bonin, M.2    Micouin, L.3
  • 70
    • 0000081676 scopus 로고
    • Synthesis of esters of 3-(2-aminoethyl) -1H-indole-2-acetic acid and 3-(2-aminoethyl)-1H-indole-2-malonic acid (= 2-[3-(2-aminoethyl)-1H-indol-2-yl] propanedioic acid). 4th communication on indoles, indolenines, and indolines
    • Mahboobi, S. and Bernauer, K. (1988) Synthesis of esters of 3-(2-aminoethyl) -1H-indole-2-acetic acid and 3-(2-aminoethyl)-1H-indole-2-malonic acid (= 2-[3-(2-aminoethyl)-1H-indol-2-yl] propanedioic acid). 4th communication on indoles, indolenines, and indolines. Helv. Chim. Acta, 71 (8), 2034-2041.
    • (1988) Helv. Chim. Acta , vol.71 , Issue.8 , pp. 2034-2041
    • Mahboobi, S.1    Bernauer, K.2
  • 71
    • 0000238887 scopus 로고
    • Intramolecular and intermolecular oxidative coupling reactions by a new iron complex [Fe(DMF) 3 Cl 2][FeCl 4]
    • Tobinaga, S. and Kotani, E. (1972) Intramolecular and intermolecular oxidative coupling reactions by a new iron complex [Fe(DMF) 3 Cl 2][FeCl 4]. J. Am. Chem. Soc., 94 (1), 309-310
    • (1972) J. Am. Chem. Soc. , vol.94 , Issue.1 , pp. 309-310
    • Tobinaga, S.1    Kotani, E.2
  • 72
    • 0000867157 scopus 로고
    • Oxidative coupling of ketone enolates by ferric chloride
    • Frazier, R.H., Jr. and Harlow, R.L. (1980) Oxidative coupling of ketone enolates by ferric chloride. J. Org. Chem., 45 (26), 5408-5411.
    • (1980) J. Org. Chem. , vol.45 , Issue.26 , pp. 5408-5411
    • Frazier Jr., R.H.1    Harlow, R.L.2
  • 73
    • 0027260840 scopus 로고
    • A novel one-flask cyclopentannulation involving a dilithiomethane equivalent as a β-connector of two enones A highly efficient total synthesis of (±)-hirsutene
    • Cohen, T., McNamara, K., Kuzemko, M.A., Ramig, K., Landi, J.J., Jr. and Dong, Y. (1993) A novel one-flask cyclopentannulation involving a dilithiomethane equivalent as a β-connector of two enones. A highly efficient total synthesis of (±)-hirsutene. Tetrahedron, 49 (36), 7931-7942
    • (1993) Tetrahedron , vol.49 , Issue.36 , pp. 7931-7942
    • Cohen, T.1    McNamara, K.2    Kuzemko, M.A.3    Ramig, K.4    Landi Jr., J.J.5    Dong, Y.6
  • 74
    • 0000338089 scopus 로고
    • Oxidative coupling of the enolate anion of (1 R)-(+)-verbenone with Fe(III) and Cu(II) salts Two modes of conjoining this bicyclic ketone across a benzene ring
    • Paquette, L.A., Bzowej, E.I., Branan, B.M. and Stanton, K.J. (1995) Oxidative coupling of the enolate anion of (1 R)-(+)-verbenone with Fe(III) and Cu(II) salts. Two modes of conjoining this bicyclic ketone across a benzene ring. J. Org. Chem., 60 (22), 7277-7283
    • (1995) J. Org. Chem. , vol.60 , Issue.22 , pp. 7277-7283
    • Paquette, L.A.1    Bzowej, E.I.2    Branan, B.M.3    Stanton, K.J.4
  • 76
    • 26844522419 scopus 로고
    • Reactions of carbonyl compounds with Grignard reagents in the presence of cerium chloride
    • Imamoto, T., Takiyama, N., Nakamura, K., Hatajima, T. and Kamiya, Y. (1989) Reactions of carbonyl compounds with Grignard reagents in the presence of cerium chloride. J. Am. Chem. Soc., 111 (12), 4392-4398.
    • (1989) J. Am. Chem. Soc. , vol.111 , Issue.12 , pp. 4392-4398
    • Imamoto, T.1    Takiyama, N.2    Nakamura, K.3    Hatajima, T.4    Kamiya, Y.5
  • 77
    • 84987474385 scopus 로고
    • SCOOPY-reaktionen: stereoselektivität der allyl-alkohol-synthese via betain -ylide
    • Schlosser, M. and Coffinet, D. (1971) SCOOPY-reaktionen: stereoselektivität der allyl-alkohol-synthese via betain -ylide. Synthesis, (7), 380-381.
    • (1971) Synthesis , Issue.7 , pp. 380-381
    • Schlosser, M.1    Coffinet, D.2
  • 78
    • 33748695353 scopus 로고    scopus 로고
    • A unified synthetic approach to the pyrazinone dragmacidins
    • Garg, N.K. and Stoltz, B.M. (2006) A unified synthetic approach to the pyrazinone dragmacidins. Chem. Commun., (36), 3769-3779.
    • (2006) Chem. Commun. , Issue.36 , pp. 3769-3779
    • Garg, N.K.1    Stoltz, B.M.2
  • 79
    • 0037032310 scopus 로고    scopus 로고
    • The first total synthesis of dragmacidin D
    • Garg, N.K., Sarpong, R. and Stoltz, B.M. (2002) The first total synthesis of dragmacidin D. J. Am. Chem. Soc., 124 (44), 13179-13184.
    • (2002) J. Am. Chem. Soc. , vol.124 , Issue.44 , pp. 13179-13184
    • Garg, N.K.1    Sarpong, R.2    Stoltz, B.M.3
  • 80
    • 0034000795 scopus 로고    scopus 로고
    • Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl) pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid
    • Jiang, B. and Gu, X.-H. (2000) Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl) pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid. Bioorg. Med. Chem., 8 (2), 363-371
    • (2000) Bioorg. Med. Chem. , vol.8 , Issue.2 , pp. 363-371
    • Jiang, B.1    Gu, X.-H.2
  • 81
    • 0034235571 scopus 로고    scopus 로고
    • Syntheses of bis(3 ′-indolyl)-2(1H) -pyrazinones
    • Jiang, B. and Gu, X.-H. (2000) Syntheses of bis(3 ′-indolyl)-2(1H) -pyrazinones. Heterocycles, 53 (7), 1559-1568
    • (2000) Heterocycles , vol.53 , Issue.7 , pp. 1559-1568
    • Jiang, B.1    Gu, X.-H.2
  • 82
    • 0037016989 scopus 로고    scopus 로고
    • Enantioselective synthesis of the aminoimidazole segment of dragmacidin D
    • Yang, C.-G., Wang, J. and Jiang, B. (2002) Enantioselective synthesis of the aminoimidazole segment of dragmacidin D. Tetrahedron Lett., 43 (6), 1063-1066
    • (2002) Tetrahedron Lett , vol.43 , Issue.6 , pp. 1063-1066
    • Yang, C.-G.1    Wang, J.2    Jiang, B.3
  • 83
    • 0037149689 scopus 로고    scopus 로고
    • Synthesis of marine sponge bisindole alkaloids dihydrohamacanthins
    • Miyake, F.Y., Yakushijin, K. and Horne, D.A. (2002) Synthesis of marine sponge bisindole alkaloids dihydrohamacanthins. Org. Lett., 4 (6), 941-943
    • (2002) Org. Lett. , vol.4 , Issue.6 , pp. 941-943
    • Miyake, F.Y.1    Yakushijin, K.2    Horne, D.A.3
  • 84
    • 0037184886 scopus 로고    scopus 로고
    • Preparing functional bis(indole) pyrazine by stepwise cross-coupling reactions: an efficient method to construct the skeleton of dragmacidin D
    • Yang, C.-G., Liu, G. and Jiang, B. (2002) Preparing functional bis(indole) pyrazine by stepwise cross-coupling reactions: an efficient method to construct the skeleton of dragmacidin D. J. Org. Chem., 67 (26), 9392-9396
    • (2002) J. Org. Chem. , vol.67 , Issue.26 , pp. 9392-9396
    • Yang, C.-G.1    Liu, G.2    Jiang, B.3
  • 85
    • 28844484645 scopus 로고    scopus 로고
    • Dragmacidin E synthesis studies Preparation of a model cycloheptannelated indole fragment
    • Feldman, K.S. and Ngernmeesri, P. (2005) Dragmacidin E synthesis studies. Preparation of a model cycloheptannelated indole fragment. Org. Lett., 7 (24), 5449-5452
    • (2005) Org. Lett. , vol.7 , Issue.24 , pp. 5449-5452
    • Feldman, K.S.1    Ngernmeesri, P.2
  • 86
    • 33750380198 scopus 로고    scopus 로고
    • A strategy for the total synthesis of dragmacidin E Construction of the core ring system
    • Huntley, R.J. and Funk, R.L. (2006) A strategy for the total synthesis of dragmacidin E. Construction of the core ring system. Org. Lett., 8 (21), 4775-4778.
    • (2006) Org. Lett. , vol.8 , Issue.21 , pp. 4775-4778
    • Huntley, R.J.1    Funk, R.L.2
  • 87
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura, N. and Suzuki, A. (1995) Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev., 95 (7), 2457-2483
    • (1995) Chem. Rev. , vol.95 , Issue.7 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 88
    • 27144488370 scopus 로고    scopus 로고
    • Carbon-carbon bonding made easy
    • Suzuki, A. (2005) Carbon-carbon bonding made easy. Chem. Commun., (38), 4759-4763
    • (2005) Chem. Commun. , Issue.38 , pp. 4759-4763
    • Suzuki, A.1
  • 89
    • 51349111666 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-coupling reactions of alkylboronic acid derivatives or alkyltrifluoroborates with aryl, alkenyl or alkyl halides and triflates
    • Doucet, H. (2008) Suzuki-Miyaura cross-coupling reactions of alkylboronic acid derivatives or alkyltrifluoroborates with aryl, alkenyl or alkyl halides and triflates. Eur. J. Org. Chem., (12), 2013-2030.
    • (2008) Eur. J. Org. Chem. , Issue.12 , pp. 2013-2030
    • Doucet, H.1
  • 92
    • 0842323485 scopus 로고    scopus 로고
    • D-Quinic acid, a versatile chiron in organic synthesis
    • Huang, P.-Q. (1999) D-Quinic acid, a versatile chiron in organic synthesis. Youji Huaxue, 19 (4), 364-373
    • (1999) Youji Huaxue , vol.19 , Issue.4 , pp. 364-373
    • Huang, P.-Q.1
  • 93
    • 0031029295 scopus 로고    scopus 로고
    • Total synthesis of (-)-reserpine using the chiron approach
    • Hanessian, S., Pan, J., Carnell, A., Bouchard, H. and Lesage, L. (1997) Total synthesis of (-)-reserpine using the chiron approach. J. Org. Chem., 62 (3), 465-473
    • (1997) J. Org. Chem. , vol.62 , Issue.3 , pp. 465-473
    • Hanessian, S.1    Pan, J.2    Carnell, A.3    Bouchard, H.4    Lesage, L.5
  • 95
    • 3142737499 scopus 로고    scopus 로고
    • Palladium catalyzed aerobic dehydrogenation: from alcohols to indoles and asymmetric catalysis
    • Stoltz, B.M. (2004) Palladium catalyzed aerobic dehydrogenation: from alcohols to indoles and asymmetric catalysis. C hem. Lett., 3 3 (4), 362-367
    • (2004) C hem. Lett. , vol.3 , Issue.4 , pp. 362-367
    • Stoltz, B.M.1
  • 96
    • 0038034779 scopus 로고    scopus 로고
    • Palladium -catalyzed oxidative Wacker cyclizations in nonpolar organic solvents with molecular oxygen: a stepping stone to asymmetric aerobic cyclizations
    • Trend, R.M., Ramtohul, Y.K., Ferreira, E.M. and Stoltz, B.M. (2003) Palladium -catalyzed oxidative Wacker cyclizations in nonpolar organic solvents with molecular oxygen: a stepping stone to asymmetric aerobic cyclizations. Angew. Chem. Int. Ed., 42 (25), 2892-2895
    • (2003) Angew. Chem. Int. Ed. , vol.42 , Issue.25 , pp. 2892-2895
    • Trend, R.M.1    Ramtohul, Y.K.2    Ferreira, E.M.3    Stoltz, B.M.4
  • 97
    • 0041624424 scopus 로고    scopus 로고
    • Catalytic C - H Bond functionalization with palladium(II): aerobic oxidative annulations of indoles
    • Ferreira, E.M. and Stoltz, B.M. (2003) Catalytic C - H Bond functionalization with palladium(II): aerobic oxidative annulations of indoles. J. Am. Chem. Soc., 125 (32), 9578-9579
    • (2003) J. Am. Chem. Soc. , vol.125 , Issue.32 , pp. 9578-9579
    • Ferreira, E.M.1    Stoltz, B.M.2
  • 98
    • 10044267678 scopus 로고    scopus 로고
    • Direct oxidative Heck cyclizations: intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans
    • Zhang, H., Ferreira, E.M. and Stoltz, B.M. (2004) Direct oxidative Heck cyclizations: intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans. A ngew. Chem. Int. Ed., 43 (45), 6144-6148.
    • (2004) A ngew. Chem. Int. Ed. , vol.43 , Issue.45 , pp. 6144-6148
    • Zhang, H.1    Ferreira, E.M.2    Stoltz, B.M.3
  • 99
    • 35548938629 scopus 로고    scopus 로고
    • Origin of regioselectivity in palladium-catalyzed cross-coupling reactions of polyhalogenated heterocycles
    • Legault, C.Y., Garcia, Y., Merlic, C.A. and Houk, K.N. (2007) Origin of regioselectivity in palladium-catalyzed cross-coupling reactions of polyhalogenated heterocycles. J. Am. Chem. Soc., 129 (42), 12664-12665
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.42 , pp. 12664-12665
    • Legault, C.Y.1    Garcia, Y.2    Merlic, C.A.3    Houk, K.N.4
  • 100
    • 70249115196 scopus 로고    scopus 로고
    • Theoretical bond dissociation energies of halo-heterocycles: trends and relationships to regioselectivity in palladium-catalyzed cross-coupling reactions
    • Garcia, Y., Schoenebeck, F., Legault, C.Y., Merlic, C.A. and Houk, K.N. (2009) Theoretical bond dissociation energies of halo-heterocycles: trends and relationships to regioselectivity in palladium-catalyzed cross-coupling reactions. J. Am. Chem. Soc., 131 (18), 6632-6639.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.18 , pp. 6632-6639
    • Garcia, Y.1    Schoenebeck, F.2    Legault, C.Y.3    Merlic, C.A.4    Houk, K.N.5
  • 101
    • 0001653842 scopus 로고
    • über eine neue art der umlagerung von oximen (New kind of rearrangement of oximes)
    • Neber, P.W. and Friedolsheim, A.V. (1926)über eine neue art der umlagerung von oximen (New kind of rearrangement of oximes). Justus Liebigs Ann. Chem., 449 (1), 109-134
    • (1926) Justus Liebigs Ann. Chem. , vol.449 , Issue.1 , pp. 109-134
    • Neber, P.W.1    Friedolsheim, A.V.2
  • 102
    • 0002143293 scopus 로고
    • The rearrangement of ketoxime O-sulfonates to amino ketones (the Neber rearrangement)
    • O'Brien, C. (1964) The rearrangement of ketoxime O-sulfonates to amino ketones (the Neber rearrangement). Chem. Rev., 64 (2), 81-89.
    • (1964) Chem. Rev. , vol.64 , Issue.2 , pp. 81-89
    • O'Brien, C.1
  • 103
    • 37049099627 scopus 로고
    • High-field 13 C N.M.R. evidence for the formation of [1,2-13 C]acetate from [2-13 C]acetate during the biosynthesis of penitrem A by Penicillium crustosum
    • De Jesus, A.E., Hull, W.E., Steyn, P.S., van Heerden, F.R., Vleggaar, R. and Wessels, P.L. (1982) High-field 13 C N.M.R. evidence for the formation of [1,2-13 C]acetate from [2-13 C]acetate during the biosynthesis of penitrem A by Penicillium crustosum. J. Chem. Soc., Chem. Commun., (15), 837-838
    • (1982) J. Chem. Soc., Chem. Commun. , Issue.15 , pp. 837-838
    • De Jesus, A.E.1    Hull, W.E.2    Steyn, P.S.3    van Heerden, F.R.4    Vleggaar, R.5    Wessels, P.L.6
  • 106
    • 37049094175 scopus 로고
    • Tremorgenic mycotoxins from Penicillium crustosum: isolation of penitrems A-F and the structure elucidation and absolute configuration of penitrem A
    • De Jesus, A.E., Steyn, P.S., van Heerden, F.R., Vleggaar, R., Wessels, P.L. and Hull, W.E. (1983) Tremorgenic mycotoxins from Penicillium crustosum: isolation of penitrems A-F and the structure elucidation and absolute configuration of penitrem A. J. Chem. Soc., Perkin Trans. 1, (8), 1847-1856.
    • (1983) J. Chem. Soc., Perkin Trans. , vol.1 , Issue.8 , pp. 1847-1856
    • De Jesus, A.E.1    Steyn, P.S.2    van Heerden, F.R.3    Vleggaar, R.4    Wessels, P.L.5    Hull, W.E.6
  • 107
    • 0000969843 scopus 로고
    • Principe et applications d'une nouvelle methode de determination des configurations dite 'par dedoublement partiel.'
    • Horeau, A. (1961) Principe et applications d'une nouvelle methode de determination des configurations dite 'par dedoublement partiel.' Tetrahedron Lett., 2 (15), 506-512
    • (1961) Tetrahedron Lett , vol.2 , Issue.15 , pp. 506-512
    • Horeau, A.1
  • 108
    • 0037770556 scopus 로고
    • The absolute configuration of some caryophyllene derivatives
    • Horeau, A. and Sutherland, J.K. (1966) The absolute configuration of some caryophyllene derivatives. J. Chem. Soc. C, 247-248
    • (1966) J. Chem. Soc. C , pp. 247-248
    • Horeau, A.1    Sutherland, J.K.2
  • 109
    • 0037770547 scopus 로고
    • Determination of the absolute configuration of hydroxylated sesquiterpene lactones by Horeau's method of asymmetric esterification
    • Herz, W. and Kagan, H.B. (1967) Determination of the absolute configuration of hydroxylated sesquiterpene lactones by Horeau's method of asymmetric esterification. J. Org. Chem., 32 (1), 216-218.
    • (1967) J. Org. Chem. , vol.32 , Issue.1 , pp. 216-218
    • Herz, W.1    Kagan, H.B.2
  • 110
    • 2442666555 scopus 로고    scopus 로고
    • Radical and palladium-catalyzed cyclizations to cyclobutenes: an entry to the BCD ring system of penitrem D
    • Rivkin, A., González-López de Turiso, F., Nagashima, T. and Curran, D.P. (2004) Radical and palladium-catalyzed cyclizations to cyclobutenes: an entry to the BCD ring system of penitrem D. J. Org. Chem., 69 (11), 3719-3725.
    • (2004) J. Org. Chem. , vol.69 , Issue.11 , pp. 3719-3725
    • Rivkin, A.1    González-López de Turiso, F.2    Nagashima, T.3    Curran, D.P.4
  • 111
    • 0024518004 scopus 로고
    • Tremorgenic indole alkaloid studies 6. Preparation of an advanced intermediate for the synthesis of penitrem D. Synthesis of an indole oxocane
    • Smith, A.B., III, Haseltine, J.N. and Visnick, M. (1989) Tremorgenic indole alkaloid studies. 6. Preparation of an advanced intermediate for the synthesis of penitrem D. Synthesis of an indole oxocane. Tetrahedron, 45 (8), 2431-2449
    • (1989) Tetrahedron , vol.45 , Issue.8 , pp. 2431-2449
    • Smith III, A.B.1    Haseltine, J.N.2    Visnick, M.3
  • 112
    • 0028858548 scopus 로고
    • Tremorgenic indole alkaloids 9. Asymmetric construction of an advanced F-G-H-ring lactone precursor for the synthesis of penitrem D
    • Smith, A.B., III, Nolen, E.G., Shirai, R., Blase, F.R., Ohta, M., Chida, N., Hartz, R.A., Fitch, D.M., Clark, W.M. and Sprengeler, P.A. (1995) Tremorgenic indole alkaloids. 9. Asymmetric construction of an advanced F-G-H-ring lactone precursor for the synthesis of penitrem D. J. Org. Chem., 60 (24), 7837-7848.
    • (1995) J. Org. Chem. , vol.60 , Issue.24 , pp. 7837-7848
    • Smith III, A.B.1    Nolen, E.G.2    Shirai, R.3    Blase, F.R.4    Ohta, M.5    Chida, N.6    Hartz, R.A.7    Fitch, D.M.8    Clark, W.M.9    Sprengeler, P.A.10
  • 113
    • 0007171346 scopus 로고
    • An expedient synthesis of substituted indoles
    • Smith, A.B., III and Visnick, M. (1985) An expedient synthesis of substituted indoles. Tetrahedron Lett., 26 (32), 3757-3760
    • (1985) Tetrahedron Lett , vol.26 , Issue.32 , pp. 3757-3760
    • Smith III, A.B.1    Visnick, M.2
  • 114
    • 0001150685 scopus 로고
    • Organometallic reagents in synthesis: a new protocol for construction of the indole nucleus
    • Smith, A.B., III, Visnick, M., Haseltine, J.N. and Sprengeler, P.A. (1986) Organometallic reagents in synthesis: a new protocol for construction of the indole nucleus. Tetrahedron, 42 (11), 2957-2969.
    • (1986) Tetrahedron , vol.42 , Issue.11 , pp. 2957-2969
    • Smith III, A.B.1    Visnick, M.2    Haseltine, J.N.3    Sprengeler, P.A.4
  • 115
    • 84987456868 scopus 로고
    • A procedure for the preparation of (S)-8a-methyl-3,4,8,8a -tetrahydro-1,6(2 H,7 H) -naphthalenedione
    • Gutzwiller, J., Buchschacher, P. and Fürst, A. (1977) A procedure for the preparation of (S)-8a-methyl-3,4,8,8a -tetrahydro-1,6(2 H,7 H) -naphthalenedione. Synthesis, (3), 167-168.
    • (1977) Synthesis , Issue.3 , pp. 167-168
    • Gutzwiller, J.1    Buchschacher, P.2    Fürst, A.3
  • 116
    • 0013624593 scopus 로고
    • Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide
    • Parikh, J.R. and Doering, W.v.E. (1967) Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide. J. Am. Chem. Soc., 89 (21), 5505-5507.
    • (1967) J. Am. Chem. Soc. , vol.89 , Issue.21 , pp. 5505-5507
    • Parikh, J.R.1    Doering, W.V.E.2
  • 117
    • 0032926111 scopus 로고    scopus 로고
    • Oxidized welwitindolinones from terrestrial Fischerella spp
    • Jimenez, J.I., Huber, U., Moore, R.E. and Patterson, G.M.L. (1999) Oxidized welwitindolinones from terrestrial Fischerella spp. J. Nat. Prod., 62 (4), 569-572.
    • (1999) J. Nat. Prod. , vol.62 , Issue.4 , pp. 569-572
    • Jimenez, J.I.1    Huber, U.2    Moore, R.E.3    Patterson, G.M.L.4
  • 118
    • 0001598577 scopus 로고
    • Hapalindoles: new alkaloids from the blue-green alga Hapalosiphon fontinalis
    • Moore, R.E., Cheuk, C. and Patterson, G.M.L. (1984) Hapalindoles: new alkaloids from the blue-green alga Hapalosiphon fontinalis. J. Am. Chem. Soc., 106 (21), 6456-6457
    • (1984) J. Am. Chem. Soc. , vol.106 , Issue.21 , pp. 6456-6457
    • Moore, R.E.1    Cheuk, C.2    Patterson, G.M.L.3
  • 120
    • 0344555621 scopus 로고
    • Unusual cyclopropane -containing hapalindolinones from a cultured cyanobacterium
    • Schwartz, R.E., Hirsch, C.F., Springer, J.P., Pettibone, D.J. and Zink, D.L. (1987) Unusual cyclopropane -containing hapalindolinones from a cultured cyanobacterium. J. Org. Chem., 52 (16), 3704-3706
    • (1987) J. Org. Chem. , vol.52 , Issue.16 , pp. 3704-3706
    • Schwartz, R.E.1    Hirsch, C.F.2    Springer, J.P.3    Pettibone, D.J.4    Zink, D.L.5
  • 121
    • 0023236009 scopus 로고
    • Fontonamide and anhydrohapaloxindole A, two new alkaloids from the blue-green alga Hapalosiphon fontinalis
    • Moore, R.E., Yang, X.-Q.G. and Patterson, G.M.L. (1987) Fontonamide and anhydrohapaloxindole A, two new alkaloids from the blue-green alga Hapalosiphon fontinalis. J. Org. Chem., 52 (17), 3773-3777
    • (1987) J. Org. Chem. , vol.52 , Issue.17 , pp. 3773-3777
    • Moore, R.E.1    Yang, X.-Q.2    Patterson, G.M.L.3
  • 123
    • 0026725094 scopus 로고
    • Fischerindole L, a new isonitrile from the terrestrial blue-green alga Fischerella muscicola
    • Park, A., Moore, R.E. and Patterson, G.M.L. (1992) Fischerindole L, a new isonitrile from the terrestrial blue-green alga Fischerella muscicola. Tetrahedron Lett., 33 (23), 3257-3260
    • (1992) Tetrahedron Lett , vol.33 , Issue.23 , pp. 3257-3260
    • Park, A.1    Moore, R.E.2    Patterson, G.M.L.3
  • 124
    • 0031733197 scopus 로고    scopus 로고
    • Isolation of a nitrile-containing indole alkaloid from the terrestrial blue-green alga Hapalosiphon delicatulus
    • Huber, U., Moore, R.E. and Patterson, G.M.L. (1998) Isolation of a nitrile-containing indole alkaloid from the terrestrial blue-green alga Hapalosiphon delicatulus. J. Nat. Prod., 61 (10), 1304-1306
    • (1998) J. Nat. Prod. , vol.61 , Issue.10 , pp. 1304-1306
    • Huber, U.1    Moore, R.E.2    Patterson, G.M.L.3
  • 125
    • 0029569071 scopus 로고
    • New hapalindoles from the cyanophyte Hapalosiphon laingii
    • Klein, D., Daloze, D., Braekman, J.C., Hoffmann, L. and Demoulin, V. (1995) New hapalindoles from the cyanophyte Hapalosiphon laingii. J. Nat. Prod., 58 (11), 1781-1785
    • (1995) J. Nat. Prod. , vol.58 , Issue.11 , pp. 1781-1785
    • Klein, D.1    Daloze, D.2    Braekman, J.C.3    Hoffmann, L.4    Demoulin, V.5
  • 126
    • 0344334587 scopus 로고
    • Hapalonamides and other oxidized hapalindoles from Hapalosiphon fontinalis
    • Moore, R.E., Yang, X.-Q.G., Patterson, G.M.L., Bonjouklian, R. and Smitka, T.A. (1989) Hapalonamides and other oxidized hapalindoles from Hapalosiphon fontinalis. Phytochemistry, 28 (5), 1565-1567
    • (1989) Phytochemistry , vol.28 , Issue.5 , pp. 1565-1567
    • Moore, R.E.1    Yang, X.-Q.2    Patterson, G.M.L.3    Bonjouklian, R.4    Smitka, T.A.5
  • 127
    • 33947363667 scopus 로고    scopus 로고
    • Antimicrobial ambiguines from the cyanobacterium Fischerella sp. collected in Israel
    • Raveh, A. and Carmeli, S. (2007) Antimicrobial ambiguines from the cyanobacterium Fischerella sp. collected in Israel. J. Nat. Prod., 70 (2), 196-201
    • (2007) J. Nat. Prod. , vol.70 , Issue.2 , pp. 196-201
    • Raveh, A.1    Carmeli, S.2
  • 128
    • 34548726321 scopus 로고    scopus 로고
    • Insecticidal activity of 12-epi-hapalindole J isonitrile
    • Becher, P.G., Keller, S., Jung, G., Süssmuth, R.D. and Jüttner, F. (2007) Insecticidal activity of 12-epi-hapalindole J isonitrile. Phytochemistry, 68 (19), 2493-2497
    • (2007) Phytochemistry , vol.68 , Issue.19 , pp. 2493-2497
    • Becher, P.G.1    Keller, S.2    Jung, G.3    Süssmuth, R.D.4    Jüttner, F.5
  • 129
    • 33746884706 scopus 로고    scopus 로고
    • Identification of an antimicrobial entity from the cyanobacterium Fischerella sp. isolated from bark of Azadirachta indica (Neem) tree
    • Asthana, R.K., Srivastava, A., Singh, A.P., Deepali, Singh, S.P., Nath, G., Srivastava, R. and Srivastava, B.S. (2006) Identification of an antimicrobial entity from the cyanobacterium Fischerella sp. isolated from bark of Azadirachta indica (Neem) tree. J. Appl. Phycol., 18 (1), 33-39.
    • (2006) J. Appl. Phycol. , vol.18 , Issue.1 , pp. 33-39
    • Asthana, R.K.1    Srivastava, A.2    Singh, A.P.3    Deepali4    Singh, S.P.5    Nath, G.6    Srivastava, R.7    Srivastava, B.S.8
  • 130
    • 0028944619 scopus 로고
    • Welwitindolinone analogs that reverse P-glycoprotein-mediated multiple drug resistance
    • Smith, C.D., Zilfou, J.T., Stratmann, K., Patterson, G.M.L. and Moore, R.E. (1995) Welwitindolinone analogs that reverse P-glycoprotein-mediated multiple drug resistance. Mol. Pharmacol., 47 (2), 241-247.
    • (1995) Mol. Pharmacol. , vol.47 , Issue.2 , pp. 241-247
    • Smith, C.D.1    Zilfou, J.T.2    Stratmann, K.3    Patterson, G.M.L.4    Moore, R.E.5
  • 131
    • 0042570636 scopus 로고    scopus 로고
    • Halogen cation induced stereoselective semipinacol-type rearrangement of allylic alcohols: a highly efficient approach to α-quaternary β-haloketo compounds
    • See also references therein
    • Wang, B.M., Song, Z.L., Fan, C.A., Tu, Y.Q. and Chen, W.M. (2003) Halogen cation induced stereoselective semipinacol-type rearrangement of allylic alcohols: a highly efficient approach to α-quaternary β-haloketo compounds. S ynlett, (10), 1497-1499. See also references therein.
    • (2003) S ynlett , Issue.10 , pp. 1497-1499
    • Wang, B.M.1    Song, Z.L.2    Fan, C.A.3    Tu, Y.Q.4    Chen, W.M.5
  • 133
    • 33751385716 scopus 로고
    • Improved protocols for the selective deprotection of trialkylsilyl ethers using fluorosilicic acid
    • Pilcher, A.S. and DeShong, P. (1993) Improved protocols for the selective deprotection of trialkylsilyl ethers using fluorosilicic acid. J. Org. Chem., 58 (19), 5130-5134.
    • (1993) J. Org. Chem. , vol.58 , Issue.19 , pp. 5130-5134
    • Pilcher, A.S.1    DeShong, P.2
  • 135
    • 33845278140 scopus 로고
    • Directed reduction of β-hydroxy ketones employing tetramethylammonium triacetoxyborohydride
    • Evans, D.A., Chapman, K.T. and Carreira, E.M. (1988) Directed reduction of β-hydroxy ketones employing tetramethylammonium triacetoxyborohydride. J. Am. Chem. Soc., 110 (11), 3560-3578.
    • (1988) J. Am. Chem. Soc. , vol.110 , Issue.11 , pp. 3560-3578
    • Evans, D.A.1    Chapman, K.T.2    Carreira, E.M.3
  • 136
    • 0000009327 scopus 로고
    • Sulfuranes. III. Reagent for the dehydration of alcohols
    • Martin, J.C. and Arhart, R.J. (1971) Sulfuranes. III. Reagent for the dehydration of alcohols. J. Am. Chem. Soc., 93 (17), 4327-4239.
    • (1971) J. Am. Chem. Soc. , vol.93 , Issue.17 , pp. 4327-4329
    • Martin, J.C.1    Arhart, R.J.2
  • 137
    • 0033215208 scopus 로고    scopus 로고
    • Reductive cleavage of N-O bonds in hydroxylamines and hydroxamic acid derivatives using samarium diiodide
    • Keck, G.E., Wager, T.T. and McHardy, S.F. (1999) Reductive cleavage of N-O bonds in hydroxylamines and hydroxamic acid derivatives using samarium diiodide. Tetrahedron, 55 (40), 11755-11772.
    • (1999) Tetrahedron , vol.55 , Issue.40 , pp. 11755-11772
    • Keck, G.E.1    Wager, T.T.2    McHardy, S.F.3
  • 138
    • 2942650166 scopus 로고    scopus 로고
    • Direct coupling of indoles with carbonyl compounds: short, enantioselective, gram-scale synthetic entry into the hapalindole and fischerindole alkaloid families
    • Baran, P.S. and Richter, J.M. (2004) Direct coupling of indoles with carbonyl compounds: short, enantioselective, gram-scale synthetic entry into the hapalindole and fischerindole alkaloid families. J. Am. Chem. Soc., 126 (24), 7450-7451.
    • (2004) J. Am. Chem. Soc. , vol.126 , Issue.24 , pp. 7450-7451
    • Baran, P.S.1    Richter, J.M.2
  • 139
    • 0001585871 scopus 로고
    • Reaction of allylically substituted enolates with organometallic reagents: a convenient source of enolonium ion equivalents
    • Wender, P.A., Erhardt, J.M. and Letendre, L.J. (1981) Reaction of allylically substituted enolates with organometallic reagents: a convenient source of enolonium ion equivalents. J. Am. Chem. Soc., 103 (8), 2114-2116.
    • (1981) J. Am. Chem. Soc. , vol.103 , Issue.8 , pp. 2114-2116
    • Wender, P.A.1    Erhardt, J.M.2    Letendre, L.J.3
  • 140
    • 9644281529 scopus 로고    scopus 로고
    • A new, simple procedure for the synthesis of formyl amides
    • De Luca, L., Giacomelli, G., Porcheddu, A. and Salaris, M. (2004) A new, simple procedure for the synthesis of formyl amides. Synlett, (14), 2570-2572.
    • (2004) Synlett , Issue.14 , pp. 2570-2572
    • De Luca, L.1    Giacomelli, G.2    Porcheddu, A.3    Salaris, M.4
  • 142
    • 0010596003 scopus 로고
    • Isonitrile, X. Notiz zur Darstellung von Isonitrilen aus monosubstituierten Formamiden durch Wasserabspaltung mittels Phosgen und Trialkylaminen
    • Ugi, I., Betz, W., Fetzer, U. and Offermann, K. (1961) Isonitrile, X. Notiz zur Darstellung von Isonitrilen aus monosubstituierten Formamiden durch Wasserabspaltung mittels Phosgen und Trialkylaminen. Chem. Ber., 94 (10), 2814-2816.
    • (1961) Chem. Ber. , vol.94 , Issue.10 , pp. 2814-2816
    • Ugi, I.1    Betz, W.2    Fetzer, U.3    Offermann, K.4
  • 144
    • 77957077902 scopus 로고    scopus 로고
    • Naturally occurring cyclotryptophans and cyclotryptamines
    • 1st edn (ed. S.W. Pelletier), John Wiley & Sons, Inc., New York, USA
    • Anthoni, U., Christophersen, C. and Nielson, P.H. (1999) Naturally occurring cyclotryptophans and cyclotryptamines, in Alkaloids: Chemical and Biological Perspectives, vol. 13, 1st edn (ed. S.W. Pelletier), John Wiley & Sons, Inc., New York, USA, pp. 163-236
    • (1999) Alkaloids: Chemical and Biological Perspectives , vol.13 , pp. 163-236
    • Anthoni, U.1    Christophersen, C.2    Nielson, P.H.3
  • 145
    • 77957022703 scopus 로고
    • Alkaloids of the calabar bean
    • (ed. A. Brossi), Academic Press, San Diego, CA, USA
    • Takano, S. and Ogasawara, K. (1989) Alkaloids of the calabar bean, in The Alkaloids: Chemistry and Pharmacology, vol. 36, (ed. A. Brossi), Academic Press, San Diego, CA, USA, pp. 225-251.
    • (1989) The Alkaloids: Chemistry and Pharmacology , vol.36 , pp. 225-251
    • Takano, S.1    Ogasawara, K.2
  • 146
    • 0020630435 scopus 로고
    • Steroidal alkaloids (batrachotoxins and 4 β-hydroxybatrachotoxins) 'indole alkaloids' (calycanthine and chimonanthine) and a piperidinyldipyridine alkaloid (noranabasamine) in skin extracts from the Colombian poison-dart frog Phyllobates terribilis (Dendrobatidae)
    • Tokuyama, T. and Daly, J.W. (1983) Steroidal alkaloids (batrachotoxins and 4 β-hydroxybatrachotoxins), 'indole alkaloids' (calycanthine and chimonanthine) and a piperidinyldipyridine alkaloid (noranabasamine) in skin extracts from the Colombian poison-dart frog Phyllobates terribilis (Dendrobatidae). Tetrahedron, 39 (1), 41-47
    • (1983) Tetrahedron , vol.39 , Issue.1 , pp. 41-47
    • Tokuyama, T.1    Daly, J.W.2
  • 147
    • 0027305208 scopus 로고
    • The alkaloids of Psychotria rostrata
    • Lajis, N.H., Mahmud, Z. and Toia, R.F. (1993) The alkaloids of Psychotria rostrata. Planta Med., 59 (4), 383-384
    • (1993) Planta Med , vol.59 , Issue.4 , pp. 383-384
    • Lajis, N.H.1    Mahmud, Z.2    Toia, R.F.3
  • 149
    • 0027454572 scopus 로고
    • WIN 64821 a new competitive antagonist to substance P, isolated from an Aspergillus species: structure determination and solution conformation
    • Barrow, C.J., Ping, C., Snyder, J.K., Sedlock, D.M., Sun, H.H. and Cooper, R. (1993) WIN 64821, a new competitive antagonist to substance P, isolated from an Aspergillus species: structure determination and solution conformation. J. Org. Chem., 58 (22), 6016-6021.
    • (1993) J. Org. Chem. , vol.58 , Issue.22 , pp. 6016-6021
    • Barrow, C.J.1    Ping, C.2    Snyder, J.K.3    Sedlock, D.M.4    Sun, H.H.5    Cooper, R.6
  • 150
    • 34547166889 scopus 로고    scopus 로고
    • Total synthesis of complex cyclotryptamine alkaloids: stereocontrolled construction of quaternary carbon stereocenters
    • Steven, A. and Overman, L.E. (2007) Total synthesis of complex cyclotryptamine alkaloids: stereocontrolled construction of quaternary carbon stereocenters. Angew. Chem. Int. Ed., 46 (29), 5488-5508.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , Issue.29 , pp. 5488-5508
    • Steven, A.1    Overman, L.E.2
  • 151
    • 39849108265 scopus 로고    scopus 로고
    • Concise total synthesis of (+)-WIN 64821 and (-)-ditryptophenaline
    • Movassaghi, M., Schmidt, M.A. and Ashenhurst, J.A. (2008) Concise total synthesis of (+)-WIN 64821 and (-)-ditryptophenaline. Angew. Chem. Int. Ed., 47 (8), 1485-1487.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , Issue.8 , pp. 1485-1487
    • Movassaghi, M.1    Schmidt, M.A.2    Ashenhurst, J.A.3
  • 152
    • 34250811388 scopus 로고    scopus 로고
    • Concise total synthesis of (-)-calycanthine, (+)-chimonanthine, and (+)-folicanthine
    • Movassaghi, M. and Schmidt, M.A. (2007) Concise total synthesis of (-)-calycanthine, (+)-chimonanthine, and (+)-folicanthine. Angew. Chem. Int. Ed., 46 (20), 3725-3728.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , Issue.20 , pp. 3725-3728
    • Movassaghi, M.1    Schmidt, M.A.2
  • 153
    • 4444344599 scopus 로고
    • The biosynthesis of gliotoxin and related epipolythiodioxopiperazines
    • (ed. P.S. Steyn), Academic Press, New York, USA
    • Kirby, G.W. and Robins, D.J. (1980) The biosynthesis of gliotoxin and related epipolythiodioxopiperazines, in The Biosynthesis of Mycotoxins: A Study in Secondary Metabolism (ed. P.S. Steyn), Academic Press, New York, USA, pp. 301-326.
    • (1980) The Biosynthesis of Mycotoxins: A Study in Secondary Metabolism , pp. 301-326
    • Kirby, G.W.1    Robins, D.J.2
  • 154
    • 0019463984 scopus 로고
    • Total synthesis of gliotoxin, dehydrogliotoxin and hyalodendrin
    • Fukuyama, T., Nakatsuka, S.-I. and Kishi, Y. (1981) Total synthesis of gliotoxin, dehydrogliotoxin and hyalodendrin. Tetrahedron, 37 (11), 2045-2078.
    • (1981) Tetrahedron , vol.37 , Issue.11 , pp. 2045-2078
    • Fukuyama, T.1    Nakatsuka, S.-I.2    Kishi, Y.3
  • 155
    • 0042924098 scopus 로고    scopus 로고
    • Current progress in the chemistry and pharmacology of akuammiline alkaloids
    • Ramírez, A. and García-Rubio, S. (2003) Current progress in the chemistry and pharmacology of akuammiline alkaloids. Curr. Med. Chem., 10 (18), 1891-1915.
    • (2003) Curr. Med. Chem. , vol.10 , Issue.18 , pp. 1891-1915
    • Ramírez, A.1    García-Rubio, S.2
  • 156
    • 34547095509 scopus 로고    scopus 로고
    • Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
    • Higuchi, K. and Kawasaki, T. (2007) Simple indole alkaloids and those with a nonrearranged monoterpenoid unit. Nat. Prod. Rep., 24 (4), 843-868.
    • (2007) Nat. Prod. Rep. , vol.24 , Issue.4 , pp. 843-868
    • Higuchi, K.1    Kawasaki, T.2
  • 157
    • 33748617096 scopus 로고    scopus 로고
    • Chiral phosphanyldihydrooxazoles in asymmetric catalysis: enantioselective Heck reactions
    • Loiseleur, O., Meier, P. and Pfaltz, A. (1996) Chiral phosphanyldihydrooxazoles in asymmetric catalysis: enantioselective Heck reactions. Angew. Chem. Int. Ed., 35 (2), 200-202.
    • (1996) Angew. Chem. Int. Ed. , vol.35 , Issue.2 , pp. 200-202
    • Loiseleur, O.1    Meier, P.2    Pfaltz, A.3
  • 158
    • 0027997412 scopus 로고
    • Tetrapropylammonium perruthenate, Pr 4 N + RuO 4 -, TPAP: a catalytic oxidant for organic synthesis
    • Ley, S.V., Norman, J., Griffith, W.P. and Marsden, S.P. (1994) Tetrapropylammonium perruthenate, Pr 4 N + RuO 4 -, TPAP: a catalytic oxidant for organic synthesis. Synthesis, (7), 639-666.
    • (1994) Synthesis , Issue.7 , pp. 639-666
    • Ley, S.V.1    Norman, J.2    Griffith, W.P.3    Marsden, S.P.4
  • 159
    • 0034643989 scopus 로고    scopus 로고
    • General approach for the synthesis of sarpagine/ajmaline indole alkaloids Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine
    • Wang, T. and Cook, J.M. (2000) General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine. Org. Lett., 2 (14), 2057-2059
    • (2000) Org. Lett. , vol.2 , Issue.14 , pp. 2057-2059
    • Wang, T.1    Cook, J.M.2
  • 160
    • 0037035041 scopus 로고    scopus 로고
    • Enantiospecific, stereospecific total synthesis of (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-Na -methylsarpagine as well as the total synthesis of the Alstonia bisindole macralstonidine
    • Zhao, S., Liao, X. and Cook, J.M. (2002) Enantiospecific, stereospecific total synthesis of (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-Na -methylsarpagine as well as the total synthesis of the Alstonia bisindole macralstonidine. Org. Lett., 4 (5), 687-690
    • (2002) Org. Lett. , vol.4 , Issue.5 , pp. 687-690
    • Zhao, S.1    Liao, X.2    Cook, J.M.3
  • 161
    • 0141485280 scopus 로고    scopus 로고
    • The first enantiospecific synthesis of (-)-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction The stereospecific introduction of the 19-(Z) ethylidene side chain
    • Cao, H., Yu, J., Wearing, X.Z., Zhang, C., Liu, X., Deschamps, J. and Cook, J.M. (2003) The first enantiospecific synthesis of (-)-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain. Tetrahedron Lett., 44 (43), 8013-8017
    • (2003) Tetrahedron Lett , vol.44 , Issue.43 , pp. 8013-8017
    • Cao, H.1    Yu, J.2    Wearing, X.Z.3    Zhang, C.4    Liu, X.5    Deschamps, J.6    Cook, J.M.7
  • 162
    • 0141432073 scopus 로고    scopus 로고
    • General approach for the synthesis of sarpagine indole alkaloids. Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B, (-)-alkaloid Q 3 (-)-panarine, (+)-N a-methylvellosimine, and (+)-N a-methyl-16-epipericyclivine
    • Yu, J., Wang, T., Liu, X., Deschamps, J., Flippen-Anderson, J., Liao, X. and Cook, J.M. (2003) General approach for the synthesis of sarpagine indole alkaloids. Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B, (-)-alkaloid Q 3, (-)-panarine, (+)-N a-methylvellosimine, and (+)-N a-methyl-16-epipericyclivine. J. Org. Chem., 68 (20), 7565-7581
    • (2003) J. Org. Chem. , vol.68 , Issue.20 , pp. 7565-7581
    • Yu, J.1    Wang, T.2    Liu, X.3    Deschamps, J.4    Flippen-Anderson, J.5    Liao, X.6    Cook, J.M.7
  • 163
    • 0842306887 scopus 로고    scopus 로고
    • Regiospecific, enantiospecific total synthesis of the 12-alkoxy-substituted indole alkaloids, (+)-12-methoxy-N a -methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline
    • Zhou, H., Liao, X. and Cook, J.M. (2004) Regiospecific, enantiospecific total synthesis of the 12-alkoxy-substituted indole alkaloids, (+)-12-methoxy-N a -methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline. Org. Lett., 6 (2), 249-252
    • (2004) Org. Lett. , vol.6 , Issue.2 , pp. 249-252
    • Zhou, H.1    Liao, X.2    Cook, J.M.3
  • 164
    • 18744399313 scopus 로고    scopus 로고
    • A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy -17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinol
    • Yu, J., Wearing, X.Z. and Cook, J.M. (2005) A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy -17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinol. J. Org. Chem., 70 (10), 3963-3979.
    • (2005) J. Org. Chem. , vol.70 , Issue.10 , pp. 3963-3979
    • Yu, J.1    Wearing, X.Z.2    Cook, J.M.3
  • 165
    • 0026793014 scopus 로고
    • Pyridine-derived triflating reagents: an improved preparation of vinyl triflates from metallo enolates
    • Comins, D.L. and Dehghani, A. (1992) Pyridine-derived triflating reagents: an improved preparation of vinyl triflates from metallo enolates. Tetrahedron Lett., 33 (42), 6299-6302.
    • (1992) Tetrahedron Lett , vol.33 , Issue.42 , pp. 6299-6302
    • Comins, D.L.1    Dehghani, A.2
  • 166
    • 33645689446 scopus 로고
    • Synthesis of 3-(indol-2-yl) propenoate derivatives of tryptamine, valuable intermediates for the preparation of indole alkaloids
    • Bailey, P.D. and Hollinshead, S.P. (1987) Synthesis of 3-(indol-2-yl) propenoate derivatives of tryptamine, valuable intermediates for the preparation of indole alkaloids. Tetrahedron Lett., 28 (25), 2879-2882
    • (1987) Tetrahedron Lett , vol.28 , Issue.25 , pp. 2879-2882
    • Bailey, P.D.1    Hollinshead, S.P.2
  • 167
    • 33751179178 scopus 로고    scopus 로고
    • A ring closing metathesis approach to the indole alkaloid mitralactonine
    • Chavan, S.P., Sharma, P., Sivappa, R. and Kalkote, U.R. (2006) A ring closing metathesis approach to the indole alkaloid mitralactonine. Tetrahedron Lett., 47 (52), 9301-9303.
    • (2006) Tetrahedron Lett , vol.47 , Issue.52 , pp. 9301-9303
    • Chavan, S.P.1    Sharma, P.2    Sivappa, R.3    Kalkote, U.R.4
  • 168
    • 33947093954 scopus 로고
    • Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts
    • Krapcho, A.P., Weimaster, J.F., Eldridge, J.M., Jahngen, E.G.E., Jr., Lovey, A.J. and Stephens, W.P. (1978) Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts. J. Org. Chem., 43 (1), 138-147.
    • (1978) J. Org. Chem. , vol.43 , Issue.1 , pp. 138-147
    • Krapcho, A.P.1    Weimaster, J.F.2    Eldridge, J.M.3    Jahngen Jr., E.G.E.4    Lovey, A.J.5    Stephens, W.P.6
  • 169
    • 69949115497 scopus 로고    scopus 로고
    • Total synthesis of the akuammiline alkaloid (±)-vincorine
    • Zhang, M., Huang, X., Shen, L. and Qin, Y. (2009) Total synthesis of the akuammiline alkaloid (±)-vincorine. J. Am. Chem. Soc., 131 (16), 6013-6020.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.16 , pp. 6013-6020
    • Zhang, M.1    Huang, X.2    Shen, L.3    Qin, Y.4
  • 170
    • 33947094130 scopus 로고
    • Lanthanides in organic chemistry. 1. Selective 1 2 reductions of conjugated ketones
    • Luche, J.-L. (1978) Lanthanides in organic chemistry. 1. Selective 1,2 reductions of conjugated ketones. J. Am. Chem. Soc., 100 (7), 2226-2227
    • (1978) J. Am. Chem. Soc. , vol.100 , Issue.7 , pp. 2226-2227
    • Luche, J.-L.1
  • 171
    • 33747176412 scopus 로고
    • Reduction of natural enones in the presence of cerium trichloride
    • Luche, J.-L., Rodriguez-Hahn, L. and Crabbé, P. (1978) Reduction of natural enones in the presence of cerium trichloride. J. Chem. Soc., Commun., (14), 601-602
    • (1978) J. Chem. Soc., Commun. , Issue.14 , pp. 601-602
    • Luche, J.-L.1    Rodriguez-Hahn, L.2    Crabbé, P.3
  • 172
    • 33845556313 scopus 로고
    • Lanthanoids in organic synthesis 6. The reduction of α-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspects
    • Gemal, A.L. and Luche, J.-L. (1981) Lanthanoids in organic synthesis. 6. The reduction of α-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspects. J. Am. Chem. Soc., 103 (18), 5454-5459.
    • (1981) J. Am. Chem. Soc. , vol.103 , Issue.18 , pp. 5454-5459
    • Gemal, A.L.1    Luche, J.-L.2
  • 173
    • 1542708924 scopus 로고
    • Substituent effects upon the kinetics of hydrogen transfer from triorganotin hydrides to the 5-hexen-1-yl radical
    • Pike, P.W., Gilliatt, V., Ridenour, M. and Hershberger, J.W. (1988) Substituent effects upon the kinetics of hydrogen transfer from triorganotin hydrides to the 5-hexen-1-yl radical. Organometallics, 7 (10), 2220-2223.
    • (1988) Organometallics , vol.7 , Issue.10 , pp. 2220-2223
    • Pike, P.W.1    Gilliatt, V.2    Ridenour, M.3    Hershberger, J.W.4
  • 175
    • 0025742948 scopus 로고
    • New approach to Strychnos alkaloids. Stereocontrolled total synthesis of (±)-dehydrotubifoline
    • Fevig, J.M., Marquis, R.W., Jr. and Overman, L.E. (1991) New approach to Strychnos alkaloids. Stereocontrolled total synthesis of (±)-dehydrotubifoline. J. Am. Chem. Soc., 113 (13), 5085-5086
    • (1991) J. Am. Chem. Soc. , vol.113 , Issue.13 , pp. 5085-5086
    • Fevig, J.M.1    Marquis Jr., R.W.2    Overman, L.E.3
  • 176
    • 0027231508 scopus 로고
    • General strategy for the stereocontrolled synthesis of Strychnos alkaloids: a concise synthesis of (±)-dehydrotubifoline
    • Rawal, V.H., Michoud, C. and Monestel, R. (1993) General strategy for the stereocontrolled synthesis of Strychnos alkaloids: a concise synthesis of (±)-dehydrotubifoline. J. Am. Chem. Soc., 115 (7), 3030-3031
    • (1993) J. Am. Chem. Soc. , vol.115 , Issue.7 , pp. 3030-3031
    • Rawal, V.H.1    Michoud, C.2    Monestel, R.3
  • 177
    • 0027309023 scopus 로고
    • A new, general synthetic pathway to Strychnos indole alkaloids First total synthesis of (±)-echitamidine
    • Bonjoch, J., Solé, D. and Bosch, J. (1993) A new, general synthetic pathway to Strychnos indole alkaloids. First total synthesis of (±)-echitamidine. J. Am. Chem. Soc., 115 (5), 2064-2065
    • (1993) J. Am. Chem. Soc. , vol.115 , Issue.5 , pp. 2064-2065
    • Bonjoch, J.1    Solé, D.2    Bosch, J.3
  • 178
    • 43449091279 scopus 로고    scopus 로고
    • A general synthetic entry to the pentacyclic Strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence
    • Boonsombat, J., Zhang, H., Chughtai, M.J., Hartung, J. and Padwa, A. (2008) A general synthetic entry to the pentacyclic Strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence. J. Org. Chem., 73 (9), 3539-3550.
    • (2008) J. Org. Chem. , vol.73 , Issue.9 , pp. 3539-3550
    • Boonsombat, J.1    Zhang, H.2    Chughtai, M.J.3    Hartung, J.4    Padwa, A.5
  • 179
    • 37049136877 scopus 로고
    • Total synthesis of (±)-fluorocurarine, the racemate of a calabash-curare alkaloid
    • Crawley, G.C. and Harley-Mason, J. (1971) Total synthesis of (±)-fluorocurarine, the racemate of a calabash-curare alkaloid. J. Chem. Soc. D, (13), 685-686.
    • (1971) J. Chem. Soc. D, (13) , pp. 685-686
    • Crawley, G.C.1    Harley-Mason, J.2
  • 180
    • 0030036498 scopus 로고    scopus 로고
    • Total synthesis of the Strychnos alkaloids (±)-akuammicine and (±)-norfluorocurarine from 3a-(o -nitrophenyl)hexahydroindol-4-ones by nickel(0)-promoted double cyclization
    • Solé, D., Bonjoch, J. and Bosch, J. (1996) Total synthesis of the Strychnos alkaloids (±)-akuammicine and (±)-norfluorocurarine from 3a-(o -nitrophenyl)hexahydroindol-4-ones by nickel(0)-promoted double cyclization. J. Org. Chem., 61 (13), 4194-4195
    • (1996) J. Org. Chem. , vol.61 , Issue.13 , pp. 4194-4195
    • Solé, D.1    Bonjoch, J.2    Bosch, J.3
  • 181
    • 0030840651 scopus 로고    scopus 로고
    • A general synthetic entry to Strychnos alkaloids of the curan type via a common 3a-(2 -nitrophenyl)hexahydroindol-4-one intermediate. Total syntheses of (±) -and (-)-tubifolidine, (±)-akuammicine, (±)-19,20-dihydroakuammicine, (±)-norfluorocurarine, (±)-echitamidine, and ({dot plus})-20-epilochneridine
    • Bonjoch, J., Solé, D., García-Rubio, S. and Bosch, J. (1997) A general synthetic entry to Strychnos alkaloids of the curan type via a common 3a-(2 -nitrophenyl)hexahydroindol-4-one intermediate. Total syntheses of (±) -and (-)-tubifolidine, (±)-akuammicine, (±)-19,20-dihydroakuammicine, (±)-norfluorocurarine, (±)-echitamidine, and ({dot plus})-20-epilochneridine. J. Am. Chem. Soc., 119 (31), 7230-7240.
    • (1997) J. Am. Chem. Soc. , vol.119 , Issue.31 , pp. 7230-7240
    • Bonjoch, J.1    Solé, D.2    García-Rubio, S.3    Bosch, J.4
  • 182
    • 0028234452 scopus 로고
    • A short, stereocontrolled synthesis of strychnine
    • Rawal, V.H. and Iwasa, S. (1994) A short, stereocontrolled synthesis of strychnine. J. Org. Chem., 59 (10), 2685-2686
    • (1994) J. Org. Chem. , vol.59 , Issue.10 , pp. 2685-2686
    • Rawal, V.H.1    Iwasa, S.2
  • 183
    • 0034273688 scopus 로고    scopus 로고
    • Synthesis of strychnine
    • Bonjoch, J. and Solé, D. (2000) Synthesis of strychnine. Chem. Rev., 100 (9), 3455-3482.
    • (2000) Chem. Rev. , vol.100 , Issue.9 , pp. 3455-3482
    • Bonjoch, J.1    Solé, D.2
  • 184
    • 84977692271 scopus 로고
    • Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte
    • Zincke, T. (1904) Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte. Liebigs Ann. Chem., 330 (2), 361-374
    • (1904) Liebigs Ann. Chem. , vol.330 , Issue.2 , pp. 361-374
    • Zincke, T.1
  • 185
    • 84966355313 scopus 로고
    • I. Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte
    • Zincke, T. (1904) I. Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte. Liebigs Ann. Chem., 333 (2), 296-345
    • (1904) Liebigs Ann. Chem. , vol.333 , Issue.2 , pp. 296-345
    • Zincke, T.1
  • 186
    • 84930655337 scopus 로고
    • Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte (2 Mittheilung. )
    • Zincke, T. and Wurker, W. (1904) Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsprodukte (2. Mittheilung.) Liebigs Ann. Chem., 338 (1), 107-141
    • (1904) Liebigs Ann. Chem. , vol.338 , Issue.1 , pp. 107-141
    • Zincke, T.1    Wurker, W.2
  • 187
    • 0000623925 scopus 로고
    • über eine neue, vom Pyridin derivierende Klasse von Farbstoffen
    • König, W. (1904)über eine neue, vom Pyridin derivierende Klasse von Farbstoffen. J. Prakt. Chem., 69 (1), 105-137.
    • (1904) J. Prakt. Chem. , vol.69 , Issue.1 , pp. 105-137
    • König, W.1
  • 188
    • 0028258854 scopus 로고
    • Claisen rearrangement of N-silyl ketene N,O-acetals generated from allyl N-phenylimidates Tetrahedron
    • Metz, P. and Linz, C. (1994) Claisen rearrangement of N-silyl ketene N,O-acetals generated from allyl N-phenylimidates. Tetrahedron, 50 (13), 3951-3966.
    • (1994) , vol.50 , Issue.13 , pp. 3951-3966
    • Metz, P.1    Linz, C.2
  • 189
    • 58149161579 scopus 로고    scopus 로고
    • Synthesis of δ-tributylstannyl-α, β, γ δ-unsaturated aldehydes from pyridines
    • Michels, T.D., Rhee, J.U. and Vanderwal, C.D. (2008) Synthesis of δ-tributylstannyl-α, β, γ, δ-unsaturated aldehydes from pyridines. Org. Lett., 10 (21), 4787-4790.
    • (2008) Org. Lett. , vol.10 , Issue.21 , pp. 4787-4790
    • Michels, T.D.1    Rhee, J.U.2    Vanderwal, C.D.3
  • 190
    • 38349136002 scopus 로고    scopus 로고
    • First total synthesis of trimeric indole alkaloid, psychotrimine
    • Matsuda, Y., Kitajima, M. and Takayama, H. (2008) First total synthesis of trimeric indole alkaloid, psychotrimine. Org. Lett., 10 (1), 125-128.
    • (2008) Org. Lett. , vol.10 , Issue.1 , pp. 125-128
    • Matsuda, Y.1    Kitajima, M.2    Takayama, H.3
  • 191
    • 67650320422 scopus 로고    scopus 로고
    • An expeditious synthesis of C(3)-N(1') heterodimeric indolines
    • Espejo, V.R. and Rainier, J.D. (2008) An expeditious synthesis of C(3)-N(1') heterodimeric indolines. J. Am. Chem. Soc., 130 (39), 12894-12895.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.39 , pp. 12894-12895
    • Espejo, V.R.1    Rainier, J.D.2
  • 192
    • 38349106245 scopus 로고    scopus 로고
    • Mechanistic insights into the stereocontrolled synthesis of hexahydropyrrolo[2 3-b]indoles by electrophilic activation of tryptophan derivatives
    • López, C.S., Pérez-Balado, C., Rodríguez-Graña, P. and de Lera, A.R. (2008) Mechanistic insights into the stereocontrolled synthesis of hexahydropyrrolo[2,3-b]indoles by electrophilic activation of tryptophan derivatives. Org. Lett., 10 (1), 77-80.
    • (2008) Org. Lett. , vol.10 , Issue.1 , pp. 77-80
    • López, C.S.1    Pérez-Balado, C.2    Rodríguez-Graña, P.3    de Lera, A.R.4
  • 193
    • 0004862277 scopus 로고
    • The Nicholas reaction of indoles. Propargylation of indoles with (propargyl)dicobalt hexacarbonyl cations
    • Nakagawa, M., Ma, J. and Hino, T. (1990) The Nicholas reaction of indoles. Propargylation of indoles with (propargyl)dicobalt hexacarbonyl cations. Heterocycles, 30 (1 Spec. Issue), 451-462
    • (1990) Heterocycles, 30 (1 Spec. Issue) , pp. 451-462
    • Nakagawa, M.1    Ma, J.2    Hino, T.3
  • 194
    • 0022365674 scopus 로고
    • Inverted prenylation of N b -methoxycarbonyltryptamine. Synthesis of 3a-(1,1-dimethylallyl)pyrrolo[2,3-b] indole and 2-(1 1-dimethylallyl) tryptamine derivatives
    • Hino, T., Hasumi, K., Yamaguchi, H., Taniguchi, M. and Nakagawa, M. (1985) Inverted prenylation of N b -methoxycarbonyltryptamine. Synthesis of 3a-(1,1-dimethylallyl)pyrrolo[2,3-b] indole and 2-(1,1-dimethylallyl) tryptamine derivatives. Chem. Pharm. Bull., 33 (12), 5202-5206
    • (1985) Chem. Pharm. Bull. , vol.33 , Issue.12 , pp. 5202-5206
    • Hino, T.1    Hasumi, K.2    Yamaguchi, H.3    Taniguchi, M.4    Nakagawa, M.5
  • 196
    • 11844298160 scopus 로고
    • A new synthesis of beta-carboline
    • Nakagawa, M., Matsuki, K. and Hino, T. (1983) A new synthesis of beta-carboline. Tetrahedron Lett., 24 (21), 2171-2174
    • (1983) Tetrahedron Lett , vol.24 , Issue.21 , pp. 2171-2174
    • Nakagawa, M.1    Matsuki, K.2    Hino, T.3
  • 197
    • 0008782288 scopus 로고
    • Insertion of isoprene units into indole and 3-substituted indoles in aqueous systems
    • Bocchi, V., Casanati, G. and Marchelli, R. (1978) Insertion of isoprene units into indole and 3-substituted indoles in aqueous systems. Tetrahedron, 34 (7), 929-932.
    • (1978) Tetrahedron , vol.34 , Issue.7 , pp. 929-932
    • Bocchi, V.1    Casanati, G.2    Marchelli, R.3
  • 198
    • 0001077876 scopus 로고
    • Azasulfonium salts A general method for the synthesis of indoles
    • Gassman, P.G., van Bergen, T.J., Gilbert, D.P. and Cue, B.W. (1974) Azasulfonium salts. A general method for the synthesis of indoles. J. Am. Chem. Soc., 96 (17), 5495-5508.
    • (1974) J. Am. Chem. Soc. , vol.96 , Issue.17 , pp. 5495-5508
    • Gassman, P.G.1    van Bergen, T.J.2    Gilbert, D.P.3    Cue, B.W.4
  • 199
    • 0000428035 scopus 로고
    • Synthesis of indoles via palladium -catalyzed heteroannulation of internal alkynes
    • Larock, R.C. and Yum, E.K. (1991) Synthesis of indoles via palladium -catalyzed heteroannulation of internal alkynes. J. Am. Chem. Soc., 113 (17), 6689-6690
    • (1991) J. Am. Chem. Soc. , vol.113 , Issue.17 , pp. 6689-6690
    • Larock, R.C.1    Yum, E.K.2
  • 200
    • 0035967767 scopus 로고    scopus 로고
    • Efficient asymmetric synthesis of biologically important tryptophan analogues via a palladium -mediated heteroannulation reaction
    • Ma, C., Liu, X., Li, X., Flippen-Anderson, J., Yu, S. and Cook, J.M. (2001) Efficient asymmetric synthesis of biologically important tryptophan analogues via a palladium -mediated heteroannulation reaction. J. Org. Chem., 66 (13), 4525-4542.
    • (2001) J. Org. Chem. , vol.66 , Issue.13 , pp. 4525-4542
    • Ma, C.1    Liu, X.2    Li, X.3    Flippen-Anderson, J.4    Yu, S.5    Cook, J.M.6
  • 201
    • 0034794463 scopus 로고    scopus 로고
    • A general and efficient copper catalyst for the amidation of aryl halides and the N-arylation of nitrogen heterocycles
    • Klapars, A., Antilla, J.C., Huang, X. and Buchwald, S.L. (2001) A general and efficient copper catalyst for the amidation of aryl halides and the N-arylation of nitrogen heterocycles. J. Am. Chem. Soc., 123 (31), 7727-7729
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.31 , pp. 7727-7729
    • Klapars, A.1    Antilla, J.C.2    Huang, X.3    Buchwald, S.L.4
  • 202
    • 0037009958 scopus 로고    scopus 로고
    • The copper-catalyzed N-arylation of indoles
    • Antilla, J.C., Klapars, A. and Buchwald, S.L. (2002) The copper-catalyzed N-arylation of indoles. J. Am. Chem. Soc., 124 (39), 11684-11688.
    • (2002) J. Am. Chem. Soc. , vol.124 , Issue.39 , pp. 11684-11688
    • Antilla, J.C.1    Klapars, A.2    Buchwald, S.L.3
  • 203
    • 70149111053 scopus 로고    scopus 로고
    • Enantiospecific total syntheses of kapakahines B and F
    • Newhouse, T., Lewis, C.A. and Baran, P.S. (2009) Enantiospecific total syntheses of kapakahines B and F. J. Am. Chem. Soc., 131 (18), 6360-6361.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.18 , pp. 6360-6361
    • Newhouse, T.1    Lewis, C.A.2    Baran, P.S.3
  • 204
    • 67650422535 scopus 로고    scopus 로고
    • Total synthesis and study of myrmicarin alkaloids
    • Ondrus, A.E. and Movassaghi, M. (2009) Total synthesis and study of myrmicarin alkaloids. C hem. Commun., (28), 4151-4165.
    • (2009) C hem. Commun. , Issue.28 , pp. 4151-4165
    • Ondrus, A.E.1    Movassaghi, M.2
  • 205
    • 0032516274 scopus 로고    scopus 로고
    • Synthesis of myrmicarin 217, a pyrrole[2,1,5-cd]indolizine from ants
    • Schröder, F. and Francke, W. (1998) Synthesis of myrmicarin 217, a pyrrole[2,1,5-cd]indolizine from ants. Tetrahedron, 54 (20), 5259-5264.
    • (1998) Tetrahedron , vol.54 , Issue.20 , pp. 5259-5264
    • Schröder, F.1    Francke, W.2
  • 206
    • 0034608032 scopus 로고    scopus 로고
    • First synthesis of nonracemic (R)-(+)-myrmicarin 217
    • Sayah, B., Pelloux-Léon, N. and Vallée, Y. (2000) First synthesis of nonracemic (R)-(+)-myrmicarin 217. J. Org. Chem., 65 (9), 2824-2826.
    • (2000) J. Org. Chem. , vol.65 , Issue.9 , pp. 2824-2826
    • Sayah, B.1    Pelloux-Léon, N.2    Vallée, Y.3
  • 207
    • 0038738282 scopus 로고    scopus 로고
    • Intramolecular cyclodehydration of (4 S)-(+)-4 -carboxyethyl-4-(pyrrol-1-yl)butanal as the key step in the formal synthesis of (S)-(-)-myrmicarin 217
    • Settambolo, R., Guazzelli, G. and Lazzaroni, R. (2003) Intramolecular cyclodehydration of (4 S)-(+)-4 -carboxyethyl-4-(pyrrol-1-yl)butanal as the key step in the formal synthesis of (S)-(-)-myrmicarin 217. Tetrahedron Asymmetry, 14 (11), 1447-1449.
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.11 , pp. 1447-1449
    • Settambolo, R.1    Guazzelli, G.2    Lazzaroni, R.3
  • 208
    • 0035815166 scopus 로고    scopus 로고
    • Highly regioselective Vilsmeier-Haack acylation of hexahydropyrroloindolizine
    • Sayah, B., Pelloux-Léon, N., Milet, A., Pardillos-Guindet, J. and Vallée, Y. (2001) Highly regioselective Vilsmeier-Haack acylation of hexahydropyrroloindolizine. J. Org. Chem., 66 (7), 2522-2525.
    • (2001) J. Org. Chem. , vol.66 , Issue.7 , pp. 2522-2525
    • Sayah, B.1    Pelloux-Léon, N.2    Milet, A.3    Pardillos-Guindet, J.4    Vallée, Y.5
  • 209
    • 33646126957 scopus 로고    scopus 로고
    • Dimerization of (+)-myrmicarin 215B A potential biomimetic approach to complex myrmicarin alkaloids
    • Ondrus, A.E. and Movassaghi, M. (2006) Dimerization of (+)-myrmicarin 215B. A potential biomimetic approach to complex myrmicarin alkaloids. Tetrahedron, 62 (22), 5287-5297
    • (2006) Tetrahedron , vol.62 , Issue.22 , pp. 5287-5297
    • Ondrus, A.E.1    Movassaghi, M.2
  • 210
    • 37549029806 scopus 로고    scopus 로고
    • Efficient and stereoselective dimerization of pyrroloindolizine derivatives inspired by a hypothesis for the biosynthesis of complex myrmicarin alkaloids
    • Movassaghi, M., Ondrus, A.E. and Chen, B. (2007) Efficient and stereoselective dimerization of pyrroloindolizine derivatives inspired by a hypothesis for the biosynthesis of complex myrmicarin alkaloids. J. Org. Chem., 72 (26), 10065-10074.
    • (2007) J. Org. Chem. , vol.72 , Issue.26 , pp. 10065-10074
    • Movassaghi, M.1    Ondrus, A.E.2    Chen, B.3
  • 211
    • 0034714545 scopus 로고    scopus 로고
    • An improved synthesis of functionalized biphenyl-based phosphine ligands
    • Tomori, H., Fox, J.M. and Buchwald, S.L. (2000) An improved synthesis of functionalized biphenyl-based phosphine ligands. J. Org. Chem., 65 (17), 5334-5341.
    • (2000) J. Org. Chem. , vol.65 , Issue.17 , pp. 5334-5341
    • Tomori, H.1    Fox, J.M.2    Buchwald, S.L.3
  • 212
    • 1942533561 scopus 로고    scopus 로고
    • Copper-catalyzed asymmetric conjugate reduction as a route to novel β-azaheterocyclic acid derivatives
    • Rainka, M.P., Aye, Y. and Buchwald, S.L. (2004) Copper-catalyzed asymmetric conjugate reduction as a route to novel β-azaheterocyclic acid derivatives. Proc. Natl. Acad. Sci. U.S.A., 101 (16), 5821-5823.
    • (2004) Proc. Natl. Acad. Sci. U.S.A. , vol.101 , Issue.16 , pp. 5821-5823
    • Rainka, M.P.1    Aye, Y.2    Buchwald, S.L.3
  • 213
    • 0007125186 scopus 로고
    • One-step formation of alkynes from aryl ketones
    • Tsuji, T., Watanabe, Y. and Mukaiyama, T. (1979) One-step formation of alkynes from aryl ketones. Chem. Lett., (5), 481-482.
    • (1979) Chem. Lett. , Issue.5 , pp. 481-482
    • Tsuji, T.1    Watanabe, Y.2    Mukaiyama, T.3
  • 214
    • 0026232163 scopus 로고
    • The lycopodium alkaloids
    • Ayer, W.A. (1991) The lycopodium alkaloids. Nat. Prod. Rep., 8 (5), 455-463
    • (1991) Nat. Prod. Rep. , vol.8 , Issue.5 , pp. 455-463
    • Ayer, W.A.1
  • 215
    • 11144328091 scopus 로고    scopus 로고
    • The lycopodium alkaloids
    • Ma, X. and Gang, D.R. (2004) The lycopodium alkaloids. Nat. Prod. Rep., 21 (6), 752-772
    • (2004) Nat. Prod. Rep. , vol.21 , Issue.6 , pp. 752-772
    • Ma, X.1    Gang, D.R.2
  • 218
    • 47049108428 scopus 로고    scopus 로고
    • Total synthesis of (+)-fawcettidine
    • Kozak, J.A. and Dake, G.R. (2008) Total synthesis of (+)-fawcettidine. Angew. Chem. Int. Ed., 47 (22), 4221-4223.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , Issue.22 , pp. 4221-4223
    • Kozak, J.A.1    Dake, G.R.2
  • 219
    • 47749107660 scopus 로고    scopus 로고
    • Enantioselective total synthesis of lycopodine
    • Yang, H., Carter, R.G. and Zakharov, L.N. (2008) Enantioselective total synthesis of lycopodine. J. Am. Chem. Soc., 130 (29), 9238-9239.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.29 , pp. 9238-9239
    • Yang, H.1    Carter, R.G.2    Zakharov, L.N.3
  • 220
    • 34247137978 scopus 로고    scopus 로고
    • Total syntheses of (+)-lyconadin A and (-)-lyconadin B
    • Beshore, D.C. and Smith, A.B., III (2007) Total syntheses of (+)-lyconadin A and (-)-lyconadin B. J. Am. Chem. Soc., 129 (14), 4148-4149
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.14 , pp. 4148-4149
    • Beshore, D.C.1    Smith III, A.B.2
  • 221
    • 53849087169 scopus 로고    scopus 로고
    • The lyconadins: enantioselective total syntheses of (+)-lyconadin A and (-)-lyconadin B
    • Beshore, D.C. and Smith, A.B., III (2008) The lyconadins: enantioselective total syntheses of (+)-lyconadin A and (-)-lyconadin B. J. Am. Chem. Soc., 130 (41), 13778-13789
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.41 , pp. 13778-13789
    • Beshore, D.C.1    Smith III, A.B.2
  • 222
    • 44949188548 scopus 로고    scopus 로고
    • Unified strategy for the synthesis of the 'miscellaneous' Lycopodium alkaloids: total synthesis of (±)-lyconadin A
    • Bisai, A., West, S.P. and Sarpong, R. (2008) Unified strategy for the synthesis of the 'miscellaneous' Lycopodium alkaloids: total synthesis of (±)-lyconadin A. J. Am. Chem. Soc., 130 (23), 7222-7223.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.23 , pp. 7222-7223
    • Bisai, A.1    West, S.P.2    Sarpong, R.3
  • 223
    • 47049116957 scopus 로고    scopus 로고
    • First asymmetric total syntheses of cernuane-type Lycopodium alkaloids, cernuine, and cermizine D
    • Nishikawa, Y., Kitajima, M. and Takayama, H. (2008) First asymmetric total syntheses of cernuane-type Lycopodium alkaloids, cernuine, and cermizine D. Org. Lett., 10 (10), 1987-1990.
    • (2008) Org. Lett. , vol.10 , Issue.10 , pp. 1987-1990
    • Nishikawa, Y.1    Kitajima, M.2    Takayama, H.3
  • 224
    • 0037178353 scopus 로고    scopus 로고
    • A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction
    • Morita, H. and Kobayashi, J. (2002) A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction. J. Org. Chem., 67 (15), 5378-5381.
    • (2002) J. Org. Chem. , vol.67 , Issue.15 , pp. 5378-5381
    • Morita, H.1    Kobayashi, J.2
  • 225
    • 0142186309 scopus 로고    scopus 로고
    • Free radical-mediated vinyl amination: a mild, general pyrrolidinyl enamine synthesis
    • Nugent, B.M., Williams, A.L., Prabhakaran, E.N. and Johnston, J.N. (2003) Free radical-mediated vinyl amination: a mild, general pyrrolidinyl enamine synthesis. Tetrahedron, 59 (45), 8877-8888
    • (2003) Tetrahedron , vol.59 , Issue.45 , pp. 8877-8888
    • Nugent, B.M.1    Williams, A.L.2    Prabhakaran, E.N.3    Johnston, J.N.4
  • 226
    • 0037191617 scopus 로고    scopus 로고
    • Free radical-mediated vinyl amination: access to N,N-dialkyl enamines and their β-stannyl and β-thio derivatives
    • Prabhakaran, E.N., Nugent, B.M., Williams, A.L., Nailor, K.E. and Johnston, J.N. (2002) Free radical-mediated vinyl amination: access to N,N-dialkyl enamines and their β-stannyl and β-thio derivatives. Org. Lett., 4 (24), 4197-4200.
    • (2002) Org. Lett. , vol.4 , Issue.24 , pp. 4197-4200
    • Prabhakaran, E.N.1    Nugent, B.M.2    Williams, A.L.3    Nailor, K.E.4    Johnston, J.N.5
  • 227
    • 0000836057 scopus 로고
    • Silicon-controlled allylation of 1,3-dioxo compounds by use of allyltrimethylsilane and ceric ammonium nitrate
    • Hwu, J.R., Chen, C.N. and Shiao, S.-S. (1995) Silicon-controlled allylation of 1,3-dioxo compounds by use of allyltrimethylsilane and ceric ammonium nitrate. J. Org. Chem., 60 (4), 856-862
    • (1995) J. Org. Chem. , vol.60 , Issue.4 , pp. 856-862
    • Hwu, J.R.1    Chen, C.N.2    Shiao, S.-S.3
  • 228
    • 0141674894 scopus 로고    scopus 로고
    • Solvent -dependent chemoselectivities in Ce(IV)-mediated oxidative coupling reactions
    • Zhang, Y., Raines, A.J. and Flowers, R.A., II (2003) Solvent -dependent chemoselectivities in Ce(IV)-mediated oxidative coupling reactions. Org. Lett., 5 (13), 2363-2365
    • (2003) Org. Lett. , vol.5 , Issue.13 , pp. 2363-2365
    • Zhang, Y.1    Raines, A.J.2    Flowers II, R.A.3
  • 229
    • 4644266189 scopus 로고    scopus 로고
    • Solvent -dependent chemoselectivities in additions of β-carbonyl imines to allyltrimethylsilane with CTAN
    • Zhang, Y., Raines, A.J. and Flowers, R.A., II (2004) Solvent -dependent chemoselectivities in additions of β-carbonyl imines to allyltrimethylsilane with CTAN. J. Org. Chem., 69 (19), 6267-6272.
    • (2004) J. Org. Chem. , vol.69 , Issue.19 , pp. 6267-6272
    • Zhang, Y.1    Raines, A.J.2    Flowers II, R.A.3
  • 230
    • 0021933679 scopus 로고
    • Cyclic diastereoselection as a synthetic route to quassinoids: a Claisen rearrangement based strategy for bruceantin
    • Ziegler, F.E., Klein, S.I., Pati, U.K. and Wang, T.F. (1985) Cyclic diastereoselection as a synthetic route to quassinoids: a Claisen rearrangement based strategy for bruceantin. J. Am. Chem. Soc., 107 (9), 2730-2737.
    • (1985) J. Am. Chem. Soc. , vol.107 , Issue.9 , pp. 2730-2737
    • Ziegler, F.E.1    Klein, S.I.2    Pati, U.K.3    Wang, T.F.4


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