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Volumn 16, Issue 19, 2012, Pages 2231-2289

Active methylene compounds in asymmetric organocatalytic synthesis of natural products and pharmaceutical scaffolds

Author keywords

Methylene compounds; Multi step synthesis; Natural products; Organocatalysis; Stereoselection; Total synthesis

Indexed keywords

NATURAL GASOLINE; STEREOCENTERS; STEREOSELECTIVITY;

EID: 84870229926     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527212803520290     Document Type: Article
Times cited : (15)

References (245)
  • 1
    • 33745731230 scopus 로고
    • Critik Der Urtheilskraft
    • 3. Aufl. ed.; Lagarde: Berlin
    • Kant, I., Critik der Urtheilskraft. 3. Aufl. ed.; Lagarde: Berlin, 1799; p. 482.
    • (1799) , pp. 482
    • Kant, I.1
  • 2
    • 0034654216 scopus 로고    scopus 로고
    • Proline-catalyzed direct asymmetric aldol reactions
    • List, B.; Lerner, R. A.; Barbas, C. F., Proline-catalyzed direct asymmetric aldol reactions. J. Am. Chem. Soc., 2000. 122, 2395-2396.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 2395-2396
    • List, B.1    Lerner, R.A.2    Barbas, C.F.3
  • 3
    • 0034600250 scopus 로고    scopus 로고
    • New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction
    • Ahrendt, K. A.; Borths, C. J.; MacMillan, D. W. C., New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction. J. Am. Chem. Soc., 2000. 122, 4243-4244.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 4243-4244
    • Ahrendt, K.A.1    Borths, C.J.2    Macmillan, D.W.C.3
  • 4
    • 34250684250 scopus 로고    scopus 로고
    • Organocatalytic synthesis of drugs and bioactive natural products
    • de Figueiredo, R. M.; Christmann, M., Organocatalytic synthesis of drugs and bioactive natural products. Eur. J. Org. Chem., 2007, 2575-2600.
    • (2007) Eur. J. Org. Chem , pp. 2575-2600
    • de Figueiredo, R.M.1    Christmann, M.2
  • 5
    • 77954827954 scopus 로고    scopus 로고
    • Asymmetric organocatalysis in total synthesis--a trial by fire
    • Marques-Lopez, E.; Herrera, R. P.; Christmann, M., Asymmetric organocatalysis in total synthesis--a trial by fire. Nat. Prod. Rep, 2010. 27, 1138-1167.
    • (2010) Nat. Prod. Rep , vol.27 , pp. 1138-1167
    • Marques-Lopez, E.1    Herrera, R.P.2    Christmann, M.3
  • 6
    • 77649087999 scopus 로고    scopus 로고
    • Organocatalytic cascade reactions as a new tool in total synthesis
    • Grondal, C.; Jeanty, M.; Enders, D., Organocatalytic cascade reactions as a new tool in total synthesis. Nature chemistry, 2010. 2, 167-178.
    • (2010) Nature Chemistry , vol.2 , pp. 167-178
    • Grondal, C.1    Jeanty, M.2    Enders, D.3
  • 7
    • 84555203812 scopus 로고    scopus 로고
    • Organocatalytic Michael and Friedel - Crafts reactions in enantioselective synthesis of biologically active compounds
    • Maltsev, O. V.; Beletskaya, I. P.; Zlotin, S. G., Organocatalytic Michael and Friedel - Crafts reactions in enantioselective synthesis of biologically active compounds. Russ. Chem. Rev., 2011. 80, 1067-1113.
    • (2011) Russ. Chem. Rev , vol.80 , pp. 1067-1113
    • Maltsev, O.V.1    Beletskaya, I.P.2    Zlotin, S.G.3
  • 8
    • 79959306753 scopus 로고    scopus 로고
    • An Organocatalytic Approach to the Synthesis of Six-Membered Heterocycles
    • Gasperi, T.; Punzi, P.; Migliorini, A.; Tofani, D., An Organocatalytic Approach to the Synthesis of Six-Membered Heterocycles. Curr. Org. Chem., 2011. 15, 2098-2146.
    • (2011) Curr. Org. Chem , vol.15 , pp. 2098-2146
    • Gasperi, T.1    Punzi, P.2    Migliorini, A.3    Tofani, D.4
  • 9
    • 79955587229 scopus 로고    scopus 로고
    • Advances in catalytic metal-free reductions: From bio-inspired concepts to applications in the organocatalytic synthesis of pharmaceuticals and natural products
    • Rueping, M.; Dufour, J.; Schoepke, F. R., Advances in catalytic metal-free reductions: from bio-inspired concepts to applications in the organocatalytic synthesis of pharmaceuticals and natural products. Green Chemistry, 2011. 13, 1084-1105.
    • (2011) Green Chemistry , vol.13 , pp. 1084-1105
    • Rueping, M.1    Dufour, J.2    Schoepke, F.R.3
  • 11
    • 84856615300 scopus 로고    scopus 로고
    • The Wieland-Miescher Ketone: A Journey from Organocatalysis to Natural Product Synthesis
    • Bradshaw, B.; Bonjoch, J., The Wieland-Miescher Ketone: A Journey from Organocatalysis to Natural Product Synthesis. Synlett 2012, 337-356.
    • (2012) Synlett , pp. 337-356
    • Bradshaw, B.1    Bonjoch, J.2
  • 12
    • 84859145068 scopus 로고    scopus 로고
    • Enantioselective organocatalytic alpha-heterofunctionalization of active methines
    • Russo, A.; De Fusco, C.; Lattanzi, A., Enantioselective organocatalytic alpha-heterofunctionalization of active methines. Rsc Advances 2012. 2, 385-397.
    • (2012) Rsc Advances , vol.2 , pp. 385-397
    • Russo, A.1    de Fusco, C.2    Lattanzi, A.3
  • 13
    • 46849122706 scopus 로고    scopus 로고
    • Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid
    • Carlson, E. C.; Rathbone, L. K.; Yang, H.; Collett, N. D.; Carter, R. G., Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid. J. Org. Chem., 2008. 73, 5155-5158.
    • (2008) J. Org. Chem , vol.73 , pp. 5155-5158
    • Carlson, E.C.1    Rathbone, L.K.2    Yang, H.3    Collett, N.D.4    Carter, R.G.5
  • 14
    • 37249032343 scopus 로고    scopus 로고
    • Enantioselective organocatalytic intramolecular aza-Michael reaction: A concise synthesis of (+)-sedamine, (+)-allosedamine, and (+)-coniine
    • Fustero, S.; Jimenez, D.; Moscardo, J.; Catalan, S.; del Pozo, C., Enantioselective organocatalytic intramolecular aza-Michael reaction: a concise synthesis of (+)-sedamine, (+)-allosedamine, and (+)-coniine. Org. Lett., 2007. 9, 5283-5286.
    • (2007) Org. Lett , vol.9 , pp. 5283-5286
    • Fustero, S.1    Jimenez, D.2    Moscardo, J.3    Catalan, S.4    del Pozo, C.5
  • 15
    • 55549148449 scopus 로고    scopus 로고
    • Organocatalytic Approach to Benzofused Nitrogen-Containing Heterocycles: Enantioselective Total Synthesis of (+)-Angustureine
    • Fustero, S.; Moscardo, J.; Jimenez, D.; Dolores Perez-Carrion, M.; Sanchez-Rosello, M.; del Pozo, C., Organocatalytic Approach to Benzofused Nitrogen-Containing Heterocycles: Enantioselective Total Synthesis of (+)-Angustureine. Chem. Eur. J., 2008. 14, 9868-9872.
    • (2008) Chem. Eur. J , vol.14 , pp. 9868-9872
    • Fustero, S.1    Moscardo, J.2    Jimenez, D.3    Dolores, P.-C.M.4    Sanchez-Rosello, M.5    del Pozo, C.6
  • 17
    • 34247165162 scopus 로고    scopus 로고
    • Organocatalysis in radical chemistry. Enantioselective α-oxyamination of aldehydes
    • Sibi, M. P.; Hasegawa, M., Organocatalysis in radical chemistry. Enantioselective α-oxyamination of aldehydes. J. Am. Chem. Soc., 2007. 129, 4124-4125.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 4124-4125
    • Sibi, M.P.1    Hasegawa, M.2
  • 18
    • 67749114483 scopus 로고    scopus 로고
    • Enantioselective intramolecular Friedel-Crafts-type α-arylation of aldehydes
    • Nicolaou, K. C.; Reingruber, R.; Sarlah, D.; Braese, S., Enantioselective intramolecular Friedel-Crafts-type α-arylation of aldehydes. J. Am. Chem. Soc., 2009. 131, 2086-2087.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 2086-2087
    • Nicolaou, K.C.1    Reingruber, R.2    Sarlah, D.3    Braese, S.4
  • 19
    • 69049104186 scopus 로고    scopus 로고
    • Enantioselective α-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway
    • Conrad, J. C.; Kong, J.; Laforteza, B. N.; MacMillan, D. W. C., Enantioselective α-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway. J. Am. Chem. Soc., 2009. 131, 11640-11641.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 11640-11641
    • Conrad, J.C.1    Kong, J.2    Laforteza, B.N.3    Macmillan, D.W.C.4
  • 20
    • 0030875301 scopus 로고    scopus 로고
    • A synthesis of (α)-tashiromine and formal synthesis of (+)-tashiromine utilizing a highly enantioselective pyrrole/cobaloxime l{cyrillic}-cation cyclization
    • L, G. J.; P, B. B
    • L, G. J.; P, B. B., A synthesis of (α)-tashiromine and formal synthesis of (+)-tashiromine utilizing a highly enantioselective pyrrole/cobaloxime l{cyrillic}-cation cyclization. Tetrahedron Lett., 1997. 38, 7007-7010.
    • (1997) Tetrahedron Lett , vol.38 , pp. 7007-7010
  • 21
    • 3242680937 scopus 로고    scopus 로고
    • New phlegmaranetype, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium
    • Morita, H.; Hirasawa, Y.; Shinzato, T.; Kobayashi, J., New phlegmaranetype, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium. Tetrahedron, 2004. 60, 7015-7023.
    • (2004) Tetrahedron , vol.60 , pp. 7015-7023
    • Morita, H.1    Hirasawa, Y.2    Shinzato, T.3    Kobayashi, J.4
  • 23
    • 84899468035 scopus 로고
    • The alkaloids of Lycopodium species; Lycopodium cernuum L
    • Marion, L.; Manske, R. H., The alkaloids of Lycopodium species; Lycopodium cernuum L. Can. J. Res., 1948. 26, 1.
    • (1948) Can. J. Res , vol.26 , pp. 1
    • Marion, L.1    Manske, R.H.2
  • 25
    • 0004914832 scopus 로고
    • The alkaloids of Lycopodium cernuum L. III. The synthesis of dihydrodeoxyepiallocernuine
    • Ayer, W. A.; Piers, K., The alkaloids of Lycopodium cernuum L. III. The synthesis of dihydrodeoxyepiallocernuine. Can. J. Res., 1967. 45, 451-459.
    • (1967) Can. J. Res , vol.45 , pp. 451-459
    • Ayer, W.A.1    Piers, K.2
  • 26
    • 47049116957 scopus 로고    scopus 로고
    • First asymmetric total syntheses of cernuane-type Lycopodium alkaloids, cernuine, and cermizine D
    • Nishikawa, Y.; Kitajima, M.; Takayama, H., First asymmetric total syntheses of cernuane-type Lycopodium alkaloids, cernuine, and cermizine D. Org. Lett. 2008. 10, 1987-1990.
    • (2008) Org. Lett , vol.10 , pp. 1987-1990
    • Nishikawa, Y.1    Kitajima, M.2    Takayama, H.3
  • 27
    • 58249104242 scopus 로고    scopus 로고
    • A divergent approach for the total syntheses of cernuane-type and quinolizidine-type Lycopodium alkaloids
    • Nishikawa, Y.; Kitajima, M.; Kogure, N.; Takayama, H., A divergent approach for the total syntheses of cernuane-type and quinolizidine-type Lycopodium alkaloids. Tetrahedron 2009. 65, 1608-1617.
    • (2009) Tetrahedron , vol.65 , pp. 1608-1617
    • Nishikawa, Y.1    Kitajima, M.2    Kogure, N.3    Takayama, H.4
  • 28
    • 61749096057 scopus 로고    scopus 로고
    • Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (α)-Paroxetine
    • Valero, G.; Schimer, J.; Cisarova, I.; Vesely, J.; Moyano, A.; Rios, R., Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (α)-Paroxetine. Tetrahedron Lett., 2009. 50, 1943-1946.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1943-1946
    • Valero, G.1    Schimer, J.2    Cisarova, I.3    Vesely, J.4    Moyano, A.5    Rios, R.6
  • 29
    • 60149095699 scopus 로고    scopus 로고
    • High-Yielding Synthesis of the Anti-Influenza Neuramidase Inhibitor (-)-Oseltamivir by Three One-Pot Operations
    • Ishikawa, H.; Suzuki, T.; Hayashi, Y., High-Yielding Synthesis of the Anti-Influenza Neuramidase Inhibitor (-)-Oseltamivir by Three One-Pot Operations. Angew. Chem. Int. Ed., 2009. 48, 1304-1307.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 1304-1307
    • Ishikawa, H.1    Suzuki, T.2    Hayashi, Y.3
  • 30
    • 67949124512 scopus 로고    scopus 로고
    • Concise synthesis of ricciocarpin A and discovery of a more potent analogue
    • Michrowska, A.; List, B., Concise synthesis of ricciocarpin A and discovery of a more potent analogue. Nature chemistry, 2009. 1, 225-228.
    • (2009) Nature Chemistry , vol.1 , pp. 225-228
    • Michrowska, A.1    List, B.2
  • 34
    • 62249217230 scopus 로고    scopus 로고
    • Synthesis of Kurasoin B using phase-transfer-catalyzed acylimidazole alkylation
    • Christiansen, M. A.; Butler, A. W.; Hill, A. R.; Andrus, M. B., Synthesis of Kurasoin B using phase-transfer-catalyzed acylimidazole alkylation. Synlett, 2009, 653-657.
    • (2009) Synlett , pp. 653-657
    • Christiansen, M.A.1    Butler, A.W.2    Hill, A.R.3    Andrus, M.B.4
  • 35
    • 0029860956 scopus 로고    scopus 로고
    • Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp FO-3684.1. Producing strain, fermentation, isolation, and biological activities
    • Uchida, R.; Shiomi, K.; Inokoshi, J.; Masuma, R.; Kawakubo, T.; Tanaka, H.; Iwai, Y.; Omura, S., Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp FO-3684.1. Producing strain, fermentation, isolation, and biological activities. J. Antib., 1996. 49, 932-934.
    • (1996) J. Antib , vol.49 , pp. 932-934
    • Uchida, R.1    Shiomi, K.2    Inokoshi, J.3    Masuma, R.4    Kawakubo, T.5    Tanaka, H.6    Iwai, Y.7    Omura, S.8
  • 38
    • 33750460266 scopus 로고    scopus 로고
    • Total synthesis of the hydroxyketone kurasoin A using asymmetric phase-transfer alkylation
    • Andrus, M. B.; Hicken, E. J.; Stephens, J. C.; Bedke, D. K., Total synthesis of the hydroxyketone kurasoin A using asymmetric phase-transfer alkylation. J. Org. Chem., 2006. 71, 8651-8654.
    • (2006) J. Org. Chem , vol.71 , pp. 8651-8654
    • Andrus, M.B.1    Hicken, E.J.2    Stephens, J.C.3    Bedke, D.K.4
  • 40
    • 0034087384 scopus 로고    scopus 로고
    • Highly diastereoselective alkylation of a pyroglutamate derivative with an electrophile obtained from indole. Synthesis of a potential intermediate for the preparation of the natural sweetener (-)-monatin
    • Oliveira, D. D. J.; Coelho, F., Highly diastereoselective alkylation of a pyroglutamate derivative with an electrophile obtained from indole. Synthesis of a potential intermediate for the preparation of the natural sweetener (-)-monatin. Synth. Commun., 2000. 30, 2143-2159.
    • (2000) Synth. Commun , vol.30 , pp. 2143-2159
    • Oliveira, D.D.J.1    Coelho, F.2
  • 41
    • 0025812662 scopus 로고
    • 3-Alkyl-4-aminobutyric acids - the 1st class of anticonvulsant agents that activates l-glutamic acid decarboxylase
    • Silverman, R. B.; Andruszkiewicz, R.; Nanavati, S. M.; Taylor, C. P.; Vartanian, M. G., 3-Alkyl-4-aminobutyric acids - the 1st class of anticonvulsant agents that activates l-glutamic acid decarboxylase. J. Med. Chem., 1991. 34, 2295-2298.
    • (1991) J. Med. Chem , vol.34 , pp. 2295-2298
    • Silverman, R.B.1    Andruszkiewicz, R.2    Nanavati, S.M.3    Taylor, C.P.4    Vartanian, M.G.5
  • 42
    • 44049089115 scopus 로고    scopus 로고
    • From basic science to blockbuster drug: The discovery of Lyrica
    • Silverman, R. B., From basic science to blockbuster drug: The discovery of Lyrica. Angew. Chem. Int. Ed., 2008. 47, 3500-3504.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 3500-3504
    • Silverman, R.B.1
  • 43
    • 63449111176 scopus 로고    scopus 로고
    • A Simple Organocatalytic Enantioselective Synthesis of Pregabalin
    • Bassas, O.; Huuskonen, J.; Rissanen, K.; Koskinen, A. M. P., A Simple Organocatalytic Enantioselective Synthesis of Pregabalin. Eur. J. Org. Chem., 2009. 2009, 1340-1351.
    • (2009) Eur. J. Org. Chem , vol.2009 , pp. 1340-1351
    • Bassas, O.1    Huuskonen, J.2    Rissanen, K.3    Koskinen, A.M.P.4
  • 44
    • 11844302258 scopus 로고    scopus 로고
    • Enantio- and diastereoselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea
    • Okino, T.; Hoashi, Y.; Furukawa, T.; Xu, X. N.; Takemoto, Y., Enantio- and diastereoselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea. J. Am. Chem. Soc., 2005. 127, 119-125.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 119-125
    • Okino, T.1    Hoashi, Y.2    Furukawa, T.3    Xu, X.N.4    Takemoto, Y.5
  • 45
    • 0142072631 scopus 로고    scopus 로고
    • Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts
    • Okino, T.; Hoashi, Y.; Takemoto, Y., Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts. J. Am. Chem. Soc., 2003. 125, 12672-12673.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12672-12673
    • Okino, T.1    Hoashi, Y.2    Takemoto, Y.3
  • 47
    • 0242323633 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Michael reaction of cyclic 1,3-dicarbonyl compounds and alpha,betaunsaturated ketones - A highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant
    • Halland, N.; Hansen, T.; Jorgensen, K. A., Organocatalytic asymmetric Michael reaction of cyclic 1,3-dicarbonyl compounds and alpha,betaunsaturated ketones - A highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant. Angew. Chem. Int. Ed., 2003. 42, 4955-4957.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 4955-4957
    • Halland, N.1    Hansen, T.2    Jorgensen, K.A.3
  • 48
    • 33845262220 scopus 로고    scopus 로고
    • Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin
    • Kim, H.; Yen, C.; Preston, P.; Chin, J., Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin. Org. Lett., 2006. 8, 5239-5242.
    • (2006) Org. Lett , vol.8 , pp. 5239-5242
    • Kim, H.1    Yen, C.2    Preston, P.3    Chin, J.4
  • 49
    • 33847051264 scopus 로고    scopus 로고
    • Highly enantioselective michael addition of cyclic 1,3-dicarbonyl compounds to alpha,beta-unsaturated ketones
    • Xie, J.-W.; Yue, L.; Chen, W.; Du, W.; Zhu, J.; Deng, J.-G.; Chen, Y.-C., Highly enantioselective michael addition of cyclic 1,3-dicarbonyl compounds to alpha,beta-unsaturated ketones. Org. Lett., 2007. 9, 413-415.
    • (2007) Org. Lett , vol.9 , pp. 413-415
    • Xie, J.-W.1    Yue, L.2    Chen, W.3    Du, W.4    Zhu, J.5    Deng, J.-G.6    Chen, Y.-C.7
  • 50
    • 70350159250 scopus 로고    scopus 로고
    • New Phenylglycine- Derived Primary Amine Organocatalysts for the preparation of optically active Warfarin
    • Kristensen, T. E.; Vestli, K.; Hansen, F. K.; Hansen, T., New Phenylglycine- Derived Primary Amine Organocatalysts for the preparation of optically active Warfarin. Eur. J. Org. Chem., 2009. 5185-5191.
    • (2009) Eur. J. Org. Chem , pp. 5185-5191
    • Kristensen, T.E.1    Vestli, K.2    Hansen, F.K.3    Hansen, T.4
  • 51
    • 70350153879 scopus 로고    scopus 로고
    • Organocatalytic Enantioselective Michael Addition of 4-Hydroxycoumarin to α, β- Unsaturated Ketones: A Simple Synthesis of Warfarin
    • Dong, Z.; Wang, L.; Chen, X.; Liu, X.; Lin, L.; Feng, X., Organocatalytic Enantioselective Michael Addition of 4-Hydroxycoumarin to α, β- Unsaturated Ketones: A Simple Synthesis of Warfarin. Eur. J. Org. Chem., 2009. 2009, 5192-5197.
    • (2009) Eur. J. Org. Chem , vol.2009 , pp. 5192-5197
    • Dong, Z.1    Wang, L.2    Chen, X.3    Liu, X.4    Lin, L.5    Feng, X.6
  • 53
    • 67650487039 scopus 로고    scopus 로고
    • First Enantioselective Synthesis of (R)-Convolutamydine B and E with N-(Heteroarenesulfonyl)prolinamides
    • Hara, N.; Nakamura, S.; Shibata, N.; Toru, T., First Enantioselective Synthesis of (R)-Convolutamydine B and E with N-(Heteroarenesulfonyl)prolinamides. Chem. Eur. J., 2009. 15, 6790-6793.
    • (2009) Chem. Eur. J , vol.15 , pp. 6790-6793
    • Hara, N.1    Nakamura, S.2    Shibata, N.3    Toru, T.4
  • 54
    • 70349777766 scopus 로고    scopus 로고
    • Cycle-specific organocascade catalysis: Application to olefin hydroamination, hydrooxidation, and amino-oxidation, and to natural product synthesis
    • Simmons, B.; Walji, A. M.; MacMillan, D. W. C., Cycle-specific organocascade catalysis: application to olefin hydroamination, hydrooxidation, and amino-oxidation, and to natural product synthesis. Angew. Chem. Int. Ed., 2009. 48, 4349-4353.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 4349-4353
    • Simmons, B.1    Walji, A.M.2    Macmillan, D.W.C.3
  • 55
    • 67651112161 scopus 로고    scopus 로고
    • Concise Total synthesis of (+)-Disparlure and its trans-isomer using asymmetric organocatalysis
    • Kim, S. G., Concise Total synthesis of (+)-Disparlure and its trans-isomer using asymmetric organocatalysis. Synthesis, 2009, 2418-2422.
    • (2009) Synthesis , pp. 2418-2422
    • Kim, S.G.1
  • 56
    • 68049110628 scopus 로고    scopus 로고
    • Asymmetric synthesis of (+)-Polyanthellin A
    • Campbell, M. J.; Johnson, J. S., Asymmetric synthesis of (+)-Polyanthellin A. J. Am. Chem. Soc., 2009. 131, 10370-10371.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 10370-10371
    • Campbell, M.J.1    Johnson, J.S.2
  • 59
    • 67649600829 scopus 로고    scopus 로고
    • Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: Application to the formal synthesis of (+)-physostigmine
    • Bui, T.; Syed, S.; Barbas, C. F., Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine. J. Am. Chem. Soc., 2009. 131, 8758-8759
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 8758-8759
    • Bui, T.1    Syed, S.2    Barbas, C.F.3
  • 60
    • 69149108113 scopus 로고    scopus 로고
    • Organocatalytic enantioselective synthesis of β-blockers: (S)-propranolol and (S)-naftopidil
    • Panchgalle, S. P.; Gore, R. G.; Chavan, S. P.; Kalkote, U. R., Organocatalytic enantioselective synthesis of β-blockers: (S)-propranolol and (S)-naftopidil. Tetrahedron: Asymmetry 2009. 20, 1767-1770.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1767-1770
    • Panchgalle, S.P.1    Gore, R.G.2    Chavan, S.P.3    Kalkote, U.R.4
  • 61
    • 67349149964 scopus 로고    scopus 로고
    • Total synthesis of eudesmane terpenes by siteselective C-H oxidations
    • Chen, K.; Baran, P. S., Total synthesis of eudesmane terpenes by siteselective C-H oxidations. Nature, 2009. 459, 824-828.
    • (2009) Nature , vol.459 , pp. 824-828
    • Chen, K.1    Baran, P.S.2
  • 62
    • 70349684843 scopus 로고    scopus 로고
    • Enantio- and stereoselective route to the phoslactomycin family of antibiotics: Formal synthesis of (+)-fostriecin and (+)-phoslactomycin B
    • Sarkar, S. M.; Wanzala, E. N.; Shibahara, S.; Takahashi, K.; Ishihara, J.; Hatakeyama, S., Enantio- and stereoselective route to the phoslactomycin family of antibiotics: formal synthesis of (+)-fostriecin and (+)-phoslactomycin B. Chem. Commun, 2009, 5907-5909.
    • (2009) Chem. Commun , pp. 5907-5909
    • Sarkar, S.M.1    Wanzala, E.N.2    Shibahara, S.3    Takahashi, K.4    Ishihara, J.5    Hatakeyama, S.6
  • 65
    • 0029100717 scopus 로고
    • A predictable enantioselective total synthesis of (+)-clavularin-a
    • Weinmann, H.; Winterfeldt, E., A predictable enantioselective total synthesis of (+)-clavularin-a. Synthesis, 1995, 1097-1101
    • (1995) Synthesis , pp. 1097-1101
    • Weinmann, H.1    Winterfeldt, E.2
  • 66
  • 67
    • 78249268215 scopus 로고    scopus 로고
    • A concise catalytic route to the marine sesquiterpenoids (-)-clavukerin A and (-)-isoclavukerin A
    • Knuppel, S.; Rogachev, V. O.; Metz, P., A concise catalytic route to the marine sesquiterpenoids (-)-clavukerin A and (-)-isoclavukerin A. Eur. J. Org. Chem., 2010, 6145-6148.
    • (2010) Eur. J. Org. Chem , pp. 6145-6148
    • Knuppel, S.1    Rogachev, V.O.2    Metz, P.3
  • 68
    • 76849107394 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (+)-conicol via Cascade Three-Component Organocatalysis
    • Hong, B.-C.; Kotame, P.; Tsai, C.-W.; Liao, J.-H., Enantioselective total synthesis of (+)-conicol via Cascade Three-Component Organocatalysis. Org. Lett., 2010. 12, 776-779.
    • (2010) Org. Lett , vol.12 , pp. 776-779
    • Hong, B.-C.1    Kotame, P.2    Tsai, C.-W.3    Liao, J.-H.4
  • 69
    • 0036741217 scopus 로고    scopus 로고
    • New meroterpenoids from the ascidian Aplidium conicum
    • Garrido, L.; Zubia, E.; Ortega, M. J.; Salva, J., New meroterpenoids from the ascidian Aplidium conicum. J. Nat. Prod., 2002. 65, 1328-1331.
    • (2002) J. Nat. Prod , vol.65 , pp. 1328-1331
    • Garrido, L.1    Zubia, E.2    Ortega, M.J.3    Salva, J.4
  • 71
    • 84970582452 scopus 로고
    • Studies of australian ascidians.3. a new tetrahydrocannabinol derivative from the ascidian synoicumcastellatum
    • Carroll, A. R.; Bowden, B. F.; Coll, J. C., Studies of australian ascidians.3. a new tetrahydrocannabinol derivative from the ascidian synoicumcastellatum. Aus. J. Chem., 1993. 46, 1079-1083.
    • (1993) Aus. J. Chem , vol.46 , pp. 1079-1083
    • Carroll, A.R.1    Bowden, B.F.2    Coll, J.C.3
  • 72
    • 0027717894 scopus 로고
    • Heterophylol, a phenolic compound with novel skeleton from artocarpus-heterophyllus
    • Lin, C. N.; Lu, C. M., Heterophylol, a phenolic compound with novel skeleton from artocarpus-heterophyllus. Tetrahedron Lett., 1993. 34, 8249-8250.
    • (1993) Tetrahedron Lett , vol.34 , pp. 8249-8250
    • Lin, C.N.1    Lu, C.M.2
  • 73
    • 38349102259 scopus 로고    scopus 로고
    • Nabilone for the treatment of pain in fibromyalgia
    • Skrabek, R. Q.; Gallmova, L.; Ethans, K.; Perry, D., Nabilone for the treatment of pain in fibromyalgia. J. of Pain 2008. 9, 164-173.
    • (2008) J. of Pain , vol.9 , pp. 164-173
    • Skrabek, R.Q.1    Gallmova, L.2    Ethans, K.3    Perry, D.4
  • 74
    • 70350438580 scopus 로고    scopus 로고
    • Facile synthesis of (-)-6-acetoxy-5-hexadecanolide by size-selective ring-closing/cross metathesis
    • Quinn, K. J.; Curto, J. M.; McGrath, K. P.; Biddick, N. A., Facile synthesis of (-)-6-acetoxy-5-hexadecanolide by size-selective ring-closing/cross metathesis. Tetrahedron Lett., 2009. 50, 7121-7123.
    • (2009) Tetrahedron Lett , vol.50 , pp. 7121-7123
    • Quinn, K.J.1    Curto, J.M.2    McGrath, K.P.3    Biddick, N.A.4
  • 75
    • 63849298971 scopus 로고    scopus 로고
    • A Facile Synthesis of Both Enantiomers of 6-Acetoxy-5-hexadecanolide, a Major Component of Mosquito Oviposition Attractant Pheromones
    • Singh, S.; Guiry, P. J., A Facile Synthesis of Both Enantiomers of 6-Acetoxy-5-hexadecanolide, a Major Component of Mosquito Oviposition Attractant Pheromones. Eur. J. Org. Chem., 2009, 1896-1901.
    • (2009) Eur. J. Org. Chem , pp. 1896-1901
    • Singh, S.1    Guiry, P.J.2
  • 76
    • 77958617074 scopus 로고    scopus 로고
    • Facile Synthesis of (-)-6-acetoxy-5-hexadecanolide by organocatalytic α-oxygenation-allylation-RCM Strategy
    • Park, Y.; Tae, J., Facile Synthesis of (-)-6-acetoxy-5-hexadecanolide by organocatalytic α-oxygenation-allylation-RCM Strategy. Synthesis, 2010, 3627-3630.
    • (2010) Synthesis , pp. 3627-3630
    • Park, Y.1    Tae, J.2
  • 77
    • 65949114853 scopus 로고    scopus 로고
    • Diphenylprolinol silyl ether as a catalyst in an asymmetric, catalytic and direct alpha-benzoyloxylation of aldehydes
    • Gotoh, H.; Hayashi, Y., Diphenylprolinol silyl ether as a catalyst in an asymmetric, catalytic and direct alpha-benzoyloxylation of aldehydes. Chem. Commun., 2009, 3083-3085.
    • (2009) Chem. Commun , pp. 3083-3085
    • Gotoh, H.1    Hayashi, Y.2
  • 78
    • 67749114507 scopus 로고    scopus 로고
    • Direct Asymmetric Benzoyloxylation of Aldehydes Catalyzed by 2-Tritylpyrrolidine
    • Kano, T.; Mii, H.; Maruoka, K., Direct Asymmetric Benzoyloxylation of Aldehydes Catalyzed by 2-Tritylpyrrolidine. J. Am. Chem. Soc., 2009. 131, 3450-3451.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 3450-3451
    • Kano, T.1    Mii, H.2    Maruoka, K.3
  • 80
    • 76449091692 scopus 로고    scopus 로고
    • Enantioselective synthesis of Daurichromenic Acid and Confluentin
    • Liu, K.; Woggon, W.-D., Enantioselective synthesis of Daurichromenic Acid and Confluentin. Eur. J. Org. Chem., 2010, 1033-1036.
    • (2010) Eur. J. Org. Chem , pp. 1033-1036
    • Liu, K.1    Woggon, W.-D.2
  • 82
    • 62249208038 scopus 로고    scopus 로고
    • Thieme Chemistry Journal Awardees- Where are They Now? An Asymmetric Organocatalytic Sequence towards 4a-Methyl Tetrahydroxanthones: Formal Synthesis of 4-Dehydroxydiversonol
    • Volz, N.; Broehmer, M. C.; Nieger, M.; Braese, S., Thieme Chemistry Journal Awardees- Where are They Now? An Asymmetric Organocatalytic Sequence towards 4a-Methyl Tetrahydroxanthones: Formal Synthesis of 4-Dehydroxydiversonol. Synlett, 2009, 550-553.
    • (2009) Synlett , pp. 550-553
    • Volz, N.1    Broehmer, M.C.2    Nieger, M.3    Braese, S.4
  • 83
    • 0038373585 scopus 로고    scopus 로고
    • Activities of prenylphenol derivatives from fruitbodies of Albatrellus spp. on the human and rat vanilloid receptor 1 (VR1) and characterisation of the novel natural product confluentin
    • Hellwig, V.; Nopper, R.; Mauler, F.; Freitag, J.; Liu, J. K.; Ding, Z. H.; Stadler, M., Activities of prenylphenol derivatives from fruitbodies of Albatrellus spp. on the human and rat vanilloid receptor 1 (VR1) and characterisation of the novel natural product confluentin. Archiv Der Pharmazie, 2003. 336, 119-126.
    • (2003) Archiv Der Pharmazie , vol.336 , pp. 119-126
    • Hellwig, V.1    Nopper, R.2    Mauler, F.3    Freitag, J.4    Liu, J.K.5    Ding, Z.H.6    Stadler, M.7
  • 84
    • 78650845100 scopus 로고    scopus 로고
    • The organocatalytic three-step total synthesis of (+)- frondosin B
    • Reiter, M.; Torssell, S.; Lee, S.; MacMillan, D. W. C., The organocatalytic three-step total synthesis of (+)- frondosin B. Chemical Science 2010. 1, 37-42.
    • (2010) Chemical Science , vol.1 , pp. 37-42
    • Reiter, M.1    Torssell, S.2    Lee, S.3    Macmillan, D.W.C.4
  • 85
    • 0035819958 scopus 로고    scopus 로고
    • Total synthesis and determination of the absolute configuration of frondosin B
    • Inoue, M.; Carson, M. W.; Frontier, A. J.; Danishefsky, S. J., Total synthesis and determination of the absolute configuration of frondosin B. J. Am. Chem. Soc., 2001. 123, 1878-1889.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 1878-1889
    • Inoue, M.1    Carson, M.W.2    Frontier, A.J.3    Danishefsky, S.J.4
  • 86
    • 0037012743 scopus 로고    scopus 로고
    • Concise total synthesis of (-)-frondosin B using a novel palladium-catalyzed cyclization
    • Hughes, C. C.; Trauner, D., Concise total synthesis of (-)-frondosin B using a novel palladium-catalyzed cyclization. Angew. Chem. Int. Ed., 2002. 41, 1569-1572.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 1569-1572
    • Hughes, C.C.1    Trauner, D.2
  • 87
    • 67149097939 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (-)-Frondosin B
    • Ovaska, T. V.; Sullivan, J. A.; Ovaska, S. I.; Winegrad, J. B.; Fair, J. D., Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (-)-Frondosin B. Organic letters 2009. 11, 2715-2718.
    • (2009) Organic Letters , vol.11 , pp. 2715-2718
    • Ovaska, T.V.1    Sullivan, J.A.2    Ovaska, S.I.3    Winegrad, J.B.4    Fair, J.D.5
  • 88
    • 0030984677 scopus 로고    scopus 로고
    • Frondosins, five new sesquiterpene hydroquinone derivatives with novel skeletons from the sponge Dysidea frondosa: Inhibitors of interleukin-8 receptors
    • Patil, A. D.; Freyer, A. J.; Killmer, L.; Offen, P.; Carte, B.; Jurewicz, A. J.; Johnson, R. K., Frondosins, five new sesquiterpene hydroquinone derivatives with novel skeletons from the sponge Dysidea frondosa: Inhibitors of interleukin-8 receptors. Tetrahedron, 1997. 53, 5047-5060.
    • (1997) Tetrahedron , vol.53 , pp. 5047-5060
    • Patil, A.D.1    Freyer, A.J.2    Killmer, L.3    Offen, P.4    Carte, B.5    Jurewicz, A.J.6    Johnson, R.K.7
  • 91
    • 0037060933 scopus 로고    scopus 로고
    • A short and convenient way to produce the Taxol (TM) A-ring utilizing the Shapiro reaction
    • Tormakangas, O. P.; Toivola, R. J.; Karvinen, E. K.; Koskinen, A. M. P. A short and convenient way to produce the Taxol (TM) A-ring utilizing the Shapiro reaction. Tetrahedron, 2002. 58, 2175-2181.
    • (2002) Tetrahedron , vol.58 , pp. 2175-2181
    • Tormakangas, O.P.1    Toivola, R.J.2    Karvinen, E.K.3    Koskinen, A.M.P.4
  • 92
    • 75349106430 scopus 로고    scopus 로고
    • Synthesis of chiral 3-substituted phthalides by a sequential organocatalytic enantioselective aldol-kactonization reaction. Three-step synthesis of (S)-(-)-3-butylphthalide
    • Zhang, H. Y.; Zhang, S. L.; Liu, L.; Luo, G. S.; Duan, W. H.; Wang, W., Synthesis of chiral 3-substituted phthalides by a sequential organocatalytic enantioselective aldol-kactonization reaction. Three-step synthesis of (S)-(-)-3-butylphthalide. J. Org. Chem., 2010. 75, 368-374.
    • (2010) J. Org. Chem , vol.75 , pp. 368-374
    • Zhang, H.Y.1    Zhang, S.L.2    Liu, L.3    Luo, G.S.4    Duan, W.H.5    Wang, W.6
  • 93
    • 0027723446 scopus 로고
    • Butylphthalide inhalation prolongs pentobarbital-anesthesia in adult mice
    • Sato, H.; Yorozu, H.; Yamaoka, S., Butylphthalide inhalation prolongs pentobarbital-anesthesia in adult mice. Biomed. Res.-Tokyo 1993. 14, 385-390.
    • (1993) Biomed. Res.-Tokyo , vol.14 , pp. 385-390
    • Sato, H.1    Yorozu, H.2    Yamaoka, S.3
  • 94
    • 0000779122 scopus 로고
    • Antiinsectan natural-products from fungal sclerotia
    • Gloer, J. B., Antiinsectan natural-products from fungal sclerotia. Acc. Chem. Res., 1995. 28, 343-350.
    • (1995) Acc. Chem. Res , vol.28 , pp. 343-350
    • Gloer, J.B.1
  • 95
    • 70350593870 scopus 로고    scopus 로고
    • Efficient solvent-free robinson annulation protocols for the highly enantioselective synthesis of the wieland-miescher ketone and analogues
    • Bradshaw, B.; Etxebarria-Jardi, G.; Bonjoch, J.; Viozquez, S. F.; Guillena, G.; Najera, C., Efficient solvent-free robinson annulation protocols for the highly enantioselective synthesis of the wieland-miescher ketone and analogues. Adv. Synth. Cat., 2009. 351, 2482-2490.
    • (2009) Adv. Synth. Cat , vol.351 , pp. 2482-2490
    • Bradshaw, B.1    Etxebarria-Jardi, G.2    Bonjoch, J.3    Viozquez, S.F.4    Guillena, G.5    Najera, C.6
  • 97
    • 77954729565 scopus 로고    scopus 로고
    • A Practical and Efficient Total Synthesis of Potent Insulinotropic (2S,3R,4S)-4-Hydroxyisoleucine through a Chiral N-Protected gamma-Keto-alpha-aminoester
    • Marin, S. D.; Catala, C.; Kumar, S. R.; Valleix, A.; Wagner, A.; Mioskowski, C., A Practical and Efficient Total Synthesis of Potent Insulinotropic (2S,3R,4S)-4-Hydroxyisoleucine through a Chiral N-Protected gamma-Keto-alpha-aminoester. Eur. J. Org. Chem., 2010, 3985-3989.
    • (2010) Eur. J. Org. Chem , pp. 3985-3989
    • Marin, S.D.1    Catala, C.2    Kumar, S.R.3    Valleix, A.4    Wagner, A.5    Mioskowski, C.6
  • 98
    • 0037028990 scopus 로고    scopus 로고
    • A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives
    • Cordova, A.; Watanabe, S.; Tanaka, F.; Notz, W.; Barbas, C. F., A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives. J. Am. Chem. Soc, 2002. 124, 1866-1867.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 1866-1867
    • Cordova, A.1    Watanabe, S.2    Tanaka, F.3    Notz, W.4    Barbas, C.F.5
  • 99
    • 32644439884 scopus 로고    scopus 로고
    • Catalytic enantioselective construction of allcarbon quaternary stereocenters
    • Trost, B. M.; Jiang, C. H., Catalytic enantioselective construction of allcarbon quaternary stereocenters. Synthesis, 2006, 369-396.
    • (2006) Synthesis , pp. 369-396
    • Trost, B.M.1    Jiang, C.H.2
  • 101
    • 33745602276 scopus 로고    scopus 로고
    • Quantitative structure-activity relationship studies on acetylcholinesterase enzyme inhibitory effects of Amaryllidaceae alkaloids
    • Elgorashi, E. E.; Malan, S. F.; Stafford, G. I.; van Staden, J., Quantitative structure-activity relationship studies on acetylcholinesterase enzyme inhibitory effects of Amaryllidaceae alkaloids. South African Journal of Botany 2006. 72, 224-231.
    • (2006) South African Journal of Botany , vol.72 , pp. 224-231
    • Elgorashi, E.E.1    Malan, S.F.2    Stafford, G.I.3    van Staden, J.4
  • 102
    • 33645985839 scopus 로고    scopus 로고
    • Inhibition of H- 3 Citalopram binding to the rat brain serotonin transporter by amaryllidaceae alkaloids
    • Elgorashi, E. E.; Stafford, G. I.; Jager, A. K.; Van Staden, J., Inhibition of H- 3 Citalopram binding to the rat brain serotonin transporter by amaryllidaceae alkaloids. Planta Medica 2006. 72, 470-473.
    • (2006) Planta Medica , vol.72 , pp. 470-473
    • Elgorashi, E.E.1    Stafford, G.I.2    Jager, A.K.3    van Staden, J.4
  • 103
    • 77955660112 scopus 로고    scopus 로고
    • An oxidative coupling for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine
    • Bogle, K. M.; Hirst, D. J.; Dixon, D. J., An oxidative coupling for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine. Tetrahedron, 2010. 66, 6399-6410.
    • (2010) Tetrahedron , vol.66 , pp. 6399-6410
    • Bogle, K.M.1    Hirst, D.J.2    Dixon, D.J.3
  • 104
    • 77953093516 scopus 로고    scopus 로고
    • A New Structural Motif for Bifunctional Bronsted Acid/Base Organocatalysis
    • Wakchaure, V. N.; List, B., A New Structural Motif for Bifunctional Bronsted Acid/Base Organocatalysis. Angew. Chem. Int. Ed., 2010. 49, 4136-4139.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 4136-4139
    • Wakchaure, V.N.1    List, B.2
  • 105
    • 78549243823 scopus 로고
    • Pheromone synthesis.137. A new synthesis of (+)-grandisol
    • Mori, K.; Fukamatsu, K., Pheromone synthesis.137. A new synthesis of (+)-grandisol. Lieb. Ann. Chem., 1992, 489-493.
    • (1992) Lieb. Ann. Chem , pp. 489-493
    • Mori, K.1    Fukamatsu, K.2
  • 106
    • 75749107417 scopus 로고    scopus 로고
    • Stereoselective synthesis of 3-Aryloctahydroindoles and application in a formalsynthesis of (-)-pancracine
    • Pansare, S. V.; Lingampally, R.; Kirby, R. L., Stereoselective synthesis of 3-Aryloctahydroindoles and application in a formalsynthesis of (-)-pancracine. Org. Lett., 2010. 12, 556-559.
    • (2010) Org. Lett , vol.12 , pp. 556-559
    • Pansare, S.V.1    Lingampally, R.2    Kirby, R.L.3
  • 107
    • 77955145874 scopus 로고    scopus 로고
    • Development of an enantioselective route toward the Lycopodium alkaloids: Total synthesis of lycopodine
    • Yang, H.; Carter, R. G., Development of an enantioselective route toward the Lycopodium alkaloids: total synthesis of lycopodine. J. Org. Chem., 2010. 75, 4929-38.
    • (2010) J. Org. Chem , vol.75 , pp. 4929-4938
    • Yang, H.1    Carter, R.G.2
  • 108
    • 77957583788 scopus 로고    scopus 로고
    • Catalytic asymmetric direct henry reaction of ynals: Short syntheses of (2S,3R)-(+)-xestoaminol C and (-)-codonopsinines
    • Uraguchi, D.; Nakamura, S.; Ooi, T., Catalytic asymmetric direct henry reaction of ynals: short syntheses of (2S,3R)-(+)-xestoaminol C and (-)-codonopsinines. Angew. Chem. Int. Ed., 2010. 49, 7562-7565.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 7562-7565
    • Uraguchi, D.1    Nakamura, S.2    Ooi, T.3
  • 109
    • 77953598032 scopus 로고    scopus 로고
    • An improved asymmetric total synthesis of (+)-biotin via the enantioselective desymmetrization of a meso-cyclic anhydride mediated by cinchona alkaloid-based sulfonamide
    • Xiong, F.; Chen, X. X.; Chen, F. E., An improved asymmetric total synthesis of (+)-biotin via the enantioselective desymmetrization of a meso-cyclic anhydride mediated by cinchona alkaloid-based sulfonamide. Tetrahedron-Asymmetry, 2010. 21, 665-669.
    • (2010) Tetrahedron-Asymmetry , vol.21 , pp. 665-669
    • Xiong, F.1    Chen, X.X.2    Chen, F.E.3
  • 110
    • 77950292439 scopus 로고    scopus 로고
    • A new powerful strategy for the organocatalytic asymmetric construction of a quaternary carbon stereogenic center
    • Inokoishi, Y.; Sasakura, N.; Nakano, K.; Ichikawa, Y.; Kotsuki, H., A new powerful strategy for the organocatalytic asymmetric construction of a quaternary carbon stereogenic center. Org. Lett., 2010. 12, 1616-1619.
    • (2010) Org. Lett , vol.12 , pp. 1616-1619
    • Inokoishi, Y.1    Sasakura, N.2    Nakano, K.3    Ichikawa, Y.4    Kotsuki, H.5
  • 111
    • 0021054336 scopus 로고
    • Yohimbine: A pharmacological probe for study of the α 2-adrenoreceptor
    • Goldberg, M. R.; Robertson, D., Yohimbine: a pharmacological probe for study of the α 2-adrenoreceptor. Pharm. Rev., 1983. 35, 143-80.
    • (1983) Pharm. Rev , vol.35 , pp. 143-180
    • Goldberg, M.R.1    Robertson, D.2
  • 114
    • 0027945128 scopus 로고
    • Symmetry-driven synthesis of indole alkaloids - asymmetric total syntheses of (+)-yohimbine, (-)-yohimbone, (-)-yohimbane, and (+)-alloyohimbane
    • Aube, J.; Ghosh, S.; Tanol, M. Symmetry-driven synthesis of indole alkaloids - asymmetric total syntheses of (+)-yohimbine, (-)-yohimbone, (-)-yohimbane, and (+)-alloyohimbane. J. Am. Chem. Soc., 1994. 116, 9009-9018.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 9009-9018
    • Aube, J.1    Ghosh, S.2    Tanol, M.3
  • 115
    • 43549099613 scopus 로고    scopus 로고
    • Catalytic asymmetric total synthesis of (+)-yohimbine
    • Mergott, D. J.; Zuend, S. J.; Jacobsen, E. N., Catalytic asymmetric total synthesis of (+)-yohimbine. Org. Lett., 2008. 10, 745-748.
    • (2008) Org. Lett , vol.10 , pp. 745-748
    • Mergott, D.J.1    Zuend, S.J.2    Jacobsen, E.N.3
  • 116
    • 80055088174 scopus 로고    scopus 로고
    • Total synthesis of (+)-Yohimbine via an enantioselective organocatalytic Pictet-Spengler reaction
    • Herle, B.; Wanner, M. J.; van Maarseveen, J. H.; Hiemstra, H., Total synthesis of (+)-Yohimbine via an enantioselective organocatalytic Pictet-Spengler reaction. J. Org. Chem., 2011. 76, 8907-8912.
    • (2011) J. Org. Chem , vol.76 , pp. 8907-8912
    • Herle, B.1    Wanner, M.J.2    van Maarseveen, J.H.3    Hiemstra, H.4
  • 117
    • 36749025633 scopus 로고    scopus 로고
    • Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
    • Galliford, C. V.; Scheidt, K. A., Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents. Angew. Chem. Int. Ed., 2007. 46, 8748-8758.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 8748-8758
    • Galliford, C.V.1    Scheidt, K.A.2
  • 118
    • 0037429493 scopus 로고    scopus 로고
    • Total synthesis of (-)-spirotryprostatin B
    • Meyers, C.; Carreira, E. M., Total synthesis of (-)-spirotryprostatin B. Angew. Chem. Int. Ed., 2003. 42, 694-696.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 694-696
    • Meyers, C.1    Carreira, E.M.2
  • 119
    • 34547178270 scopus 로고    scopus 로고
    • Total synthesis of spirotryprostatin B via diastereoselective prenylation
    • Trost, B. M.; Stiles, D. T., Total synthesis of spirotryprostatin B via diastereoselective prenylation. Org. Lett., 2007. 9, 2763-2766.
    • (2007) Org. Lett , vol.9 , pp. 2763-2766
    • Trost, B.M.1    Stiles, D.T.2
  • 120
    • 79955604603 scopus 로고    scopus 로고
    • Asymmetic organocatalytic 1,3-dipolar cycloaddition of azomethine ylide to methyl 2-(2-nitrophenyl)acrylate for the synthesis of diastereoisomers of spirotryprostatin A
    • Cheng, M.-N.; Wang, H.; Gong, L.-Z., Asymmetic organocatalytic 1,3-dipolar cycloaddition of azomethine ylide to methyl 2-(2-nitrophenyl)acrylate for the synthesis of diastereoisomers of spirotryprostatin A. Org. Lett., 2011. 13, 2418-2421.
    • (2011) Org. Lett , vol.13 , pp. 2418-2421
    • Cheng, M.-N.1    Wang, H.2    Gong, L.-Z.3
  • 122
    • 70949095549 scopus 로고    scopus 로고
    • Microtubule-stabilizing activity of Zampanolide, a potent macrolide isolated from the Tongan marine sponge Cacospongia mycofijiensis
    • Field, J. J.; Singh, A. J.; Kanakkanthara, A.; Halafihi, T.I.; Northcote, P. T.; Miller, J. H., Microtubule-stabilizing activity of Zampanolide, a potent macrolide isolated from the Tongan marine sponge Cacospongia mycofijiensis. J. Med. Chem., 2009. 52, 7328-7332.
    • (2009) J. Med. Chem , vol.52 , pp. 7328-7332
    • Field, J.J.1    Singh, A.J.2    Kanakkanthara, A.3    Halafihi, T.I.4    Northcote, P.T.5    Miller, J.H.6
  • 123
    • 79961087497 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (-)-Zampanolide, a potent microtubule-stabilizing agent
    • Ghosh, A. K.; Cheng, X., Enantioselective total synthesis of (-)-Zampanolide, a potent microtubule-stabilizing agent. Org. Lett., 2011. 13, 4108-4111.
    • (2011) Org. Lett. , vol.13 , pp. 4108-4111
    • Ghosh, A.K.1    Cheng, X.2
  • 124
    • 0037436454 scopus 로고    scopus 로고
    • Privileged chiral catalysts
    • Yoon, T. P.; Jacobsen, E. N. Privileged chiral catalysts. Science 2003. 299, 1691-1693.
    • (2003) Science , vol.299 , pp. 1691-1693
    • Yoon, T.P.1    Jacobsen, E.N.2
  • 125
    • 77950521746 scopus 로고    scopus 로고
    • Cinchona Alkaloids in Asymmetric Organocatalysis
    • Marcelli, T.; Hiemstra, H., Cinchona Alkaloids in Asymmetric Organocatalysis. Synthesis, 2010, 1229-1279.
    • (2010) Synthesis , pp. 1229-1279
    • Marcelli, T.1    Hiemstra, H.2
  • 126
    • 33845220042 scopus 로고    scopus 로고
    • Cupreines and cupreidines: An emerging class of bifunctional cinchona organocatalysts
    • Marcelli, T.; van Maarseveen, J. H.; Hiemstra, H., Cupreines and cupreidines: An emerging class of bifunctional cinchona organocatalysts. Angew. Chem. Int. Ed., 2006. 45, 7496-7504.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 7496-7504
    • Marcelli, T.1    van Maarseveen, J.H.2    Hiemstra, H.3
  • 127
  • 128
    • 0005519280 scopus 로고
    • Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation (AD).1. Kinetics
    • Kolb, H. C.; Andersson, P. G.; Sharpless, K. B. Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation (AD).1. Kinetics. J. Am. Chem. Soc., 1994. 116, 1278-1291.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 1278-1291
    • Kolb, H.C.1    Andersson, P.G.2    Sharpless, K.B.3
  • 129
    • 82255174969 scopus 로고    scopus 로고
    • Biscinchona alkaloids as highly efficient bifunctional organocatalysts for the asymmetric conjugate addition of malonates to nitroalkenes at ambient temperature
    • Li, F.; Li, Y.-Z.; Jia, Z.-S.; Xu, M.-H.; Tian, P.; Lin, G.-Q., Biscinchona alkaloids as highly efficient bifunctional organocatalysts for the asymmetric conjugate addition of malonates to nitroalkenes at ambient temperature. Tetrahedron, 2011. 67, 10186-10194.
    • (2011) Tetrahedron , vol.67 , pp. 10186-10194
    • Li, F.1    Li, Y.-Z.2    Jia, Z.-S.3    Xu, M.-H.4    Tian, P.5    Lin, G.-Q.6
  • 131
    • 70349925991 scopus 로고    scopus 로고
    • N-Heterocyclic Carbene-Catalyzed Generation of alpha,beta-Unsaturated Acyl Imidazoliums: Synthesis of Dihydropyranones by their Reaction with Enolates
    • Ryan, S. J.; Candish, L.; Lupton, D. W., N-Heterocyclic Carbene-Catalyzed Generation of alpha,beta-Unsaturated Acyl Imidazoliums: Synthesis of Dihydropyranones by their Reaction with Enolates. J. Am. Chem. Soc., 2009. 131, 14176-14177.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 14176-14177
    • Ryan, S.J.1    Candish, L.2    Lupton, D.W.3
  • 132
    • 81255138128 scopus 로고    scopus 로고
    • Concise formal synthesis of (-)-7-deoxyloganin via N-heterocyclic carbene catalysed rearrangement of α,α-unsaturated enol esters
    • Candish, L.; Lupton, D. W., Concise formal synthesis of (-)-7-deoxyloganin via N-heterocyclic carbene catalysed rearrangement of α,α-unsaturated enol esters. Org. Biomol. Chem., 2011. 9, 8182-8189.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 8182-8189
    • Candish, L.1    Lupton, D.W.2
  • 135
    • 0037019628 scopus 로고    scopus 로고
    • A highly enantioselective catalytic intramolecular Stetter reaction
    • Kerr, M. S.; de Alaniz, J. R.; Rovis, T., A highly enantioselective catalytic intramolecular Stetter reaction. J. Am. Chem. Soc., 2002. 124, 10298-10299.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 10298-10299
    • Kerr, M.S.1    de Alaniz, J.R.2    Rovis, T.3
  • 137
    • 33748629399 scopus 로고    scopus 로고
    • Efficient N-heterocyclic carbenecatalyzed O- to C-acyl transfer
    • Thomson, J. E.; Rix, K.; Smith, A. D., Efficient N-heterocyclic carbenecatalyzed O- to C-acyl transfer. Org. Lett., 2006. 8, 3785-3788.
    • (2006) Org. Lett , vol.8 , pp. 3785-3788
    • Thomson, J.E.1    Rix, K.2    Smith, A.D.3
  • 138
    • 79956089533 scopus 로고    scopus 로고
    • A Stereoselective Formal Synthesis of Leucascandrolide A
    • Lee, K.; Kim, H.; Hong, J., A Stereoselective Formal Synthesis of Leucascandrolide A. Org. Lett., 2011. 13, 2722-2725.
    • (2011) Org. Lett , vol.13 , pp. 2722-2725
    • Lee, K.1    Kim, H.2    Hong, J.3
  • 139
    • 0026712362 scopus 로고
    • Naturally-occurring organohalogen compounds - a survey
    • Gribble, G. W. Naturally-occurring organohalogen compounds - a survey. J. Nat. Prod., 1992. 55, 1353-1395.
    • (1992) J. Nat. Prod , vol.55 , pp. 1353-1395
    • Gribble, G.W.1
  • 140
    • 34848832308 scopus 로고    scopus 로고
    • Some recent advances in the synthesis of polycyclic imidazole-containing marine natural products
    • Weinreb, S. M., Some recent advances in the synthesis of polycyclic imidazole-containing marine natural products. Nat. Prod. Rep., 2007. 24, 931-948.
    • (2007) Nat. Prod. Rep , vol.24 , pp. 931-948
    • Weinreb, S.M.1
  • 141
    • 0031909711 scopus 로고    scopus 로고
    • Novel bromopyrrole alkaloids from the sponge Agelas dispar
    • Cafieri, F.; Fattorusso, E.; Taglialatela-Scafati, O., Novel bromopyrrole alkaloids from the sponge Agelas dispar. J. Nat. Prod., 1998. 61, 122-125.
    • (1998) J. Nat. Prod , vol.61 , pp. 122-125
    • Cafieri, F.1    Fattorusso, E.2    Taglialatela-Scafati, O.3
  • 142
    • 0034627361 scopus 로고    scopus 로고
    • Two novel pyrrole-imidazole alkaloids from the Mediterranean sponge Agelas oroides
    • Fattorusso, E.; Taglialatela-Scafati, O., Two novel pyrrole-imidazole alkaloids from the Mediterranean sponge Agelas oroides. Tetrahedron Lett., 2000. 41, 9917-9922.
    • (2000) Tetrahedron Lett , vol.41 , pp. 9917-9922
    • Fattorusso, E.1    Taglialatela-Scafati, O.2
  • 143
    • 27444436814 scopus 로고    scopus 로고
    • Syntheses of Senantiomers of hanishin, longamide B, and longamide B methyl ester from L-aspartic acid beta-methyl ester: Establishment of absolute stereochemistry
    • Patel, J.; Pelloux-Leon, N.; Minassian, F.; Vallee, Y., Syntheses of Senantiomers of hanishin, longamide B, and longamide B methyl ester from L-aspartic acid beta-methyl ester: Establishment of absolute stereochemistry. J. Org. Chem., 2005. 70, 9081-9084.
    • (2005) J. Org. Chem , vol.70 , pp. 9081-9084
    • Patel, J.1    Pelloux-Leon, N.2    Minassian, F.3    Vallee, Y.4
  • 145
    • 34250824037 scopus 로고    scopus 로고
    • Asymmetric annulation toward pyrrolopiperazinones: Concise enantioselective syntheses of pyrrole alkaloid natural products
    • Trost, B. M.; Dong, G., Asymmetric annulation toward pyrrolopiperazinones: Concise enantioselective syntheses of pyrrole alkaloid natural products. Org. Lett., 2007. 9, 2357-2359.
    • (2007) Org. Lett , vol.9 , pp. 2357-2359
    • Trost, B.M.1    Dong, G.2
  • 146
    • 78149258014 scopus 로고    scopus 로고
    • Palladium-catalyzed dynamic kinetic asymmetric transformations of vinyl aziridines with nitrogen heterocycles: Rapid access to biologically active pyrroles and indoles
    • Trost, B. M.; Osipov, M.; Dong, G., Palladium-catalyzed dynamic kinetic asymmetric transformations of vinyl aziridines with nitrogen heterocycles: rapid access to biologically active pyrroles and indoles. J. Am. Chem. Soc., 2010. 132, 15800-15807.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 15800-15807
    • Trost, B.M.1    Osipov, M.2    Dong, G.3
  • 148
    • 77957164101 scopus 로고    scopus 로고
    • Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions
    • Bae, J.-Y.; Lee, H.-J.; Youn, S.-H.; Kwon, S.-H.; Cho, C.-W., Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions. Org. Lett., 2010. 12, 4352-4355.
    • (2010) Org. Lett , vol.12 , pp. 4352-4355
    • Bae, J.-Y.1    Lee, H.-J.2    Youn, S.-H.3    Kwon, S.-H.4    Cho, C.-W.5
  • 149
    • 80054965732 scopus 로고    scopus 로고
    • Organocatalytic enantioselective formal synthesis of bromopyrrole alkaloids via aza-Michael addition
    • Lee, S. J.; Youn, S. H.; Cho, C. W., Organocatalytic enantioselective formal synthesis of bromopyrrole alkaloids via aza-Michael addition. Org. Biomol. Chem., 2011. 9, 7734-7741.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 7734-7741
    • Lee, S.J.1    Youn, S.H.2    Cho, C.W.3
  • 150
    • 80055065073 scopus 로고    scopus 로고
    • Stereoselective synthesis of 2,6-trans-tetrahydropyran via primary diamine-catalyzed oxa-conjugate addition reaction of α,α-unsaturated ketone: Total synthesis of psymberin
    • Byeon, S. R.; Park, H.; Kim, H.; Hong, J., Stereoselective synthesis of 2,6-trans-tetrahydropyran via primary diamine-catalyzed oxa-conjugate addition reaction of α,α-unsaturated ketone: total synthesis of psymberin. Org. Lett., 2011. 13, 5816-5819.
    • (2011) Org. Lett , vol.13 , pp. 5816-5819
    • Byeon, S.R.1    Park, H.2    Kim, H.3    Hong, J.4
  • 151
    • 1242296319 scopus 로고    scopus 로고
    • Antineoplastic agents. 520. Isolation and structure of irciniastatins A and B from the Indo-Pacific marine sponge Ircinia ramosa
    • Pettit, G. R.; Xu, J. P.; Chapuis, J. C.; Pettit, R. K.; Tackett, L. P.; Doubek, D. L.; Hooper, J. N. A.; Schmidt, J. M., Antineoplastic agents. 520. Isolation and structure of irciniastatins A and B from the Indo-Pacific marine sponge Ircinia ramosa. J. Med. Chem., 2004. 47, 1149-1152.
    • (2004) J. Med. Chem , vol.47 , pp. 1149-1152
    • Pettit, G.R.1    Xu, J.P.2    Chapuis, J.C.3    Pettit, R.K.4    Tackett, L.P.5    Doubek, D.L.6    Hooper, J.N.A.7    Schmidt, J.M.8
  • 152
    • 3042706094 scopus 로고    scopus 로고
    • Psymberin, a potent spongederived cytotoxin from Psammocinia distantly related to the pederin family
    • Cichewicz, R. H.; Valeriote, F. A.; Crews, P., Psymberin, a potent spongederived cytotoxin from Psammocinia distantly related to the pederin family. Org. Lett., 2004. 6, 1951-1954.
    • (2004) Org. Lett , vol.6 , pp. 1951-1954
    • Cichewicz, R.H.1    Valeriote, F.A.2    Crews, P.3
  • 153
    • 38949182994 scopus 로고    scopus 로고
    • 2,6-disubstituted tetrahydropyrans by tandem cross-metathesis/iodocyclisation
    • Hiebel, M.-A.; Pelotier, B.; Goekjian, P.; Piva, O., 2,6-disubstituted tetrahydropyrans by tandem cross-metathesis/iodocyclisation. Eur. J. Org. Chem., 2008, 713-720.
    • (2008) Eur. J. Org. Chem , pp. 713-720
    • Hiebel, M.-A.1    Pelotier, B.2    Goekjian, P.3    Piva, O.4
  • 154
    • 39149102146 scopus 로고    scopus 로고
    • Synthesis of six-membered oxygenated heterocycles through carbon-oxygen bond-forming reactions
    • Larrosa, I.; Romea, P.; Urpi, F., Synthesis of six-membered oxygenated heterocycles through carbon-oxygen bond-forming reactions. Tetrahedron, 2008. 64, 2683-2723.
    • (2008) Tetrahedron , vol.64 , pp. 2683-2723
    • Larrosa, I.1    Romea, P.2    Urpi, F.3
  • 155
    • 33646403425 scopus 로고    scopus 로고
    • Strategies for the formation of tetrahydropyran rings in the synthesis of natural products
    • Clarke, P. A.; Santos, S., Strategies for the formation of tetrahydropyran rings in the synthesis of natural products. Eur. J. Org. Chem., 2006, 2045-2053.
    • (2006) Eur. J. Org. Chem , pp. 2045-2053
    • Clarke, P.A.1    Santos, S.2
  • 156
    • 67149141768 scopus 로고    scopus 로고
    • Tandem rutheniumcatalyzed redox isomerization-O-conjugate addition: An atom-economic synthesis of cyclic ethers
    • Trost, B. M.; Gutierrez, A. C.; Livingston, R. C., Tandem rutheniumcatalyzed redox isomerization-O-conjugate addition: an atom-economic synthesis of cyclic ethers. Org. Lett., 2009. 11, 2539-2542.
    • (2009) Org. Lett , vol.11 , pp. 2539-2542
    • Trost, B.M.1    Gutierrez, A.C.2    Livingston, R.C.3
  • 157
    • 70349777766 scopus 로고    scopus 로고
    • Cycle-specific organocascade catalysis: Application to olefin hydroamination, hydrooxidation, and amino-oxidation, and to natural product synthesis
    • Simmons, B.; Walji, A. M.; MacMillan, D. W., Cycle-specific organocascade catalysis: application to olefin hydroamination, hydrooxidation, and amino-oxidation, and to natural product synthesis. Angew. Chem. Int. Ed., 2009. 48, 4349-4353.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 4349-4353
    • Simmons, B.1    Walji, A.M.2    Macmillan, D.W.3
  • 158
    • 79960407415 scopus 로고    scopus 로고
    • Collective synthesis of natural products by means of organocascade catalysis
    • Jones, S. B.; Simmons, B.; Mastracchio, A.; MacMillan, D. W., Collective synthesis of natural products by means of organocascade catalysis. Nature 2011. 475, 183-188.
    • (2011) Nature , vol.475 , pp. 183-188
    • Jones, S.B.1    Simmons, B.2    Mastracchio, A.3    Macmillan, D.W.4
  • 159
    • 70349753180 scopus 로고    scopus 로고
    • Nine-step enantioselective total synthesis of (+)-Minfiensine
    • Jones, S. B.; Simmons, B.; MacMillan, D. W. C., Nine-step enantioselective total synthesis of (+)-Minfiensine. J. Am. Chem. Soc., 2009. 131, 13606.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 13606
    • Jones, S.B.1    Simmons, B.2    Macmillan, D.W.C.3
  • 160
    • 0027507601 scopus 로고
    • Enantioselective total synthesis of (-)-strychnine
    • Knight, S. D.; Overman, L. E.; Pairaudeau, G., Enantioselective total synthesis of (-)-strychnine. J. Am. Chem. Soc., 1993. 115, 9293-9294.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 9293-9294
    • Knight, S.D.1    Overman, L.E.2    Pairaudeau, G.3
  • 161
    • 0042626234 scopus 로고    scopus 로고
    • A novel and general synthetic pathway to Strychnos indole alkaloids: Total syntheses of (-)-tubifoline, (-)-dehydrotubifoline, and (-)-strychnine using palladium catalyzed asymmetric allylic substitution
    • Mori, M.; Nakanishi, M.; Kajishima, D.; Sato, Y., A novel and general synthetic pathway to Strychnos indole alkaloids: Total syntheses of (-)-tubifoline, (-)-dehydrotubifoline, and (-)-strychnine using palladium catalyzed asymmetric allylic substitution. J. Am. Chem. Soc., 2003. 125, 9801-9807.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 9801-9807
    • Mori, M.1    Nakanishi, M.2    Kajishima, D.3    Sato, Y.4
  • 163
    • 0036570864 scopus 로고    scopus 로고
    • An efficient approach to Aspidosperma alkaloids via 4+2 cycloadditions of aminosiloxydienes: Stereocontrolled total synthesis of (+/-)-tabersonine. Gram-scale catalytic asymmetric syntheses of (+)-tabersonine and (+)-16-methoxytabersonine. Asymmetric syntheses of (+)-aspidospermidine and (-)-quebrachamine
    • Kozmin, S. A.; Iwama, T.; Huang, Y.; Rawal, V. H., An efficient approach to Aspidosperma alkaloids via 4+2 cycloadditions of aminosiloxydienes: Stereocontrolled total synthesis of (+/-)-tabersonine. Gram-scale catalytic asymmetric syntheses of (+)-tabersonine and (+)-16-methoxytabersonine. Asymmetric syntheses of (+)-aspidospermidine and (-)-quebrachamine. J. Am. Chem. Soc., 2002. 124, 4628-4641.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 4628-4641
    • Kozmin, S.A.1    Iwama, T.2    Huang, Y.3    Rawal, V.H.4
  • 165
    • 37049092876 scopus 로고
    • Total synthesis of (-)-kopsinilam, (-)-kopsinine, and the bis-indole alkaloids (-)-norpleiomutine and (-)-pleiomutine
    • Magnus, P.; Brown, P., Total synthesis of (-)-kopsinilam, (-)-kopsinine, and the bis-indole alkaloids (-)-norpleiomutine and (-)-pleiomutine. J. Chem. Soc.-Chem. Commun., 1985, 184-186.
    • (1985) J. Chem. Soc.-Chem. Commun , pp. 184-186
    • Magnus, P.1    Brown, P.2
  • 166
    • 0001529989 scopus 로고    scopus 로고
    • Application of ferrocenylalkyl chiral auxiliaries to syntheses of indolenine alkaloids: Enantioselective syntheses of vincadifformine, psi- and 20-epi-psivincadifformines, tabersonine, ibophyllidine, and mossambine
    • Kuehne, M. E.; Bandarage, U. K.; Hammach, A.; Li, Y. L.; Wang, T. S., Application of ferrocenylalkyl chiral auxiliaries to syntheses of indolenine alkaloids: Enantioselective syntheses of vincadifformine, psi- and 20-epi-psivincadifformines, tabersonine, ibophyllidine, and mossambine. J. Org. Chem., 1998. 63, 2172-2183.
    • (1998) J. Org. Chem , vol.63 , pp. 2172-2183
    • Kuehne, M.E.1    Bandarage, U.K.2    Hammach, A.3    Li, Y.L.4    Wang, T.S.5
  • 167
    • 78650450609 scopus 로고    scopus 로고
    • Natural products as a source of Alzheimer's drug leads
    • Williams, P.; Sorribas, A.; Howes, M.-J. R., Natural products as a source of Alzheimer's drug leads. Nat. Prod. Rep., 2011. 28, 48-77.
    • (2011) Nat. Prod. Rep , vol.28 , pp. 48-77
    • Williams, P.1    Sorribas, A.2    Howes, M.-J.R.3
  • 168
    • 23944462604 scopus 로고    scopus 로고
    • General synthesis of (1-substituted-1H-1,2,3-triazol-4-ylmethyl)-dialkylamines via a copper(I)-catalyzed three-component reaction in water
    • Yan, Z. Y.; Zhao, Y. B.; Fan, M. J.; Liu, W. M.; Liang, Y. M., General synthesis of (1-substituted-1H-1,2,3-triazol-4-ylmethyl)-dialkylamines via a copper(I)-catalyzed three-component reaction in water. Tetrahedron, 2005. 61, 9331-9337.
    • (2005) Tetrahedron , vol.61 , pp. 9331-9337
    • Yan, Z.Y.1    Zhao, Y.B.2    Fan, M.J.3    Liu, W.M.4    Liang, Y.M.5
  • 169
    • 8744304751 scopus 로고    scopus 로고
    • One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated azides
    • Feldman, A. K.; Colasson, B.; Fokin, V. V., One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated azides. Org. Lett., 2004. 6, 3897-3899.
    • (2004) Org. Lett , vol.6 , pp. 3897-3899
    • Feldman, A.K.1    Colasson, B.2    Fokin, V.V.3
  • 170
    • 80051889227 scopus 로고    scopus 로고
    • An Efficient Synthesis of a (-)-Physostigmine's Library for Identifying Potential Anti-Alzheimer's Agents
    • Wu, Y.; Wang, F. S.; Song, H.; Qin, Y., An Efficient Synthesis of a (-)-Physostigmine's Library for Identifying Potential Anti-Alzheimer's Agents. Helv. Chim. Acta 2011. 94, 1496-1505.
    • (2011) Helv. Chim. Acta , vol.94 , pp. 1496-1505
    • Wu, Y.1    Wang, F.S.2    Song, H.3    Qin, Y.4
  • 171
    • 1842732181 scopus 로고    scopus 로고
    • Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: Synthesis of (-)-flustramine B
    • Austin, J. F.; Kim, S. G.; Sinz, C. J.; Xiao, W. J.; MacMillan, D. W. C., Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: Synthesis of (-)-flustramine B. Proc. Nat. Acad. Sc. USA., 2004. 101, 5482-5487.
    • (2004) Proc. Nat. Acad. Sc. USA , vol.101 , pp. 5482-5487
    • Austin, J.F.1    Kim, S.G.2    Sinz, C.J.3    Xiao, W.J.4    Macmillan, D.W.C.5
  • 172
    • 0000978367 scopus 로고
    • Hagens gland morphology and chemical content-analysis for 3 species of parasitic wasps (hymenoptera, braconidae)
    • Williams, H. J.; Wong, M.; Wharton, R. A.; Vinson, S. B., Hagens gland morphology and chemical content-analysis for 3 species of parasitic wasps (hymenoptera, braconidae). J. Chem. Ec., 1988. 14, 1727-1736.
    • (1988) J. Chem. Ec , vol.14 , pp. 1727-1736
    • Williams, H.J.1    Wong, M.2    Wharton, R.A.3    Vinson, S.B.4
  • 173
    • 33748765782 scopus 로고    scopus 로고
    • 4,5-Didehydro-7-silyloxymethyl-2-oxepanone and formal total syntheses of Hagen's gland lactones and trans-kumausynes
    • Agrawal, D.; Sriramurthy, V.; Yadav, V. K., 4,5-Didehydro-7-silyloxymethyl-2-oxepanone and formal total syntheses of Hagen's gland lactones and trans-kumausynes. Tetrahedron Lett., 2006. 47, 7615-7618.
    • (2006) Tetrahedron Lett , vol.47 , pp. 7615-7618
    • Agrawal, D.1    Sriramurthy, V.2    Yadav, V.K.3
  • 174
    • 33745810919 scopus 로고    scopus 로고
    • Chiron approach for the synthesis of (5RS)-Hagen's gland lactones from diacetone-D-mannose
    • Banda, G.; Chakravarthy, I. E., Chiron approach for the synthesis of (5RS)-Hagen's gland lactones from diacetone-D-mannose. Tetrahedron-Asymmetry, 2006. 17, 1684-1687.
    • (2006) Tetrahedron-Asymmetry , vol.17 , pp. 1684-1687
    • Banda, G.1    Chakravarthy, I.E.2
  • 175
    • 0034607727 scopus 로고    scopus 로고
    • Pd(II)Cl-2 mediated oxidative cyclisation of hydroxy-vinylfurans to lactols: Synthesis of Hagen's gland lactones
    • Mereyala, H. B.; Gadikota, R. R.; Sunder, K. S.; Shailaja, S., Pd(II)Cl-2 mediated oxidative cyclisation of hydroxy-vinylfurans to lactols: Synthesis of Hagen's gland lactones. Tetrahedron 2000. 56, 3021-3026.
    • (2000) Tetrahedron , vol.56 , pp. 3021-3026
    • Mereyala, H.B.1    Gadikota, R.R.2    Sunder, K.S.3    Shailaja, S.4
  • 177
    • 8844259726 scopus 로고    scopus 로고
    • The core structures of roseophilin and the prodigiosin alkaloids define a new class of protein tyrosine phosphatase inhibitors
    • Furstner, A.; Reinecke, K.; Prinz, H.; Waldmann, H., The core structures of roseophilin and the prodigiosin alkaloids define a new class of protein tyrosine phosphatase inhibitors. Chem. Bio Chem. 2004. 5, 1575-1579.
    • (2004) Chem. Bio Chem , vol.5 , pp. 1575-1579
    • Furstner, A.1    Reinecke, K.2    Prinz, H.3    Waldmann, H.4
  • 178
    • 17744417463 scopus 로고    scopus 로고
    • Chemistry and biology of roseophilin and the prodigiosin alkaloids: A survey of the last 2500 years
    • Furstner, A., Chemistry and biology of roseophilin and the prodigiosin alkaloids: A survey of the last 2500 years. Angew. Chem. Int. Ed., 2003. 42, 3582-3603.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 3582-3603
    • Furstner, A.1
  • 180
    • 0026031214 scopus 로고
    • Butyl-meta-cycloheptylprodiginine - a revision of the structure of the former ortho-isomer
    • Laatsch, H.; Kellner, M.; Weyland, H., Butyl-meta-cycloheptylprodiginine - a revision of the structure of the former ortho-isomer. J. Antib., 1991. 44, 187-191.
    • (1991) J. Antib , vol.44 , pp. 187-191
    • Laatsch, H.1    Kellner, M.2    Weyland, H.3
  • 181
    • 0014691401 scopus 로고
    • Metacycloprodigiosin, a tripyrrole pigment from Streptomyces longisporus ruber
    • Wasserman, H. H.; Rodgers, G. C.; Keith, D. D., Metacycloprodigiosin, a tripyrrole pigment from Streptomyces longisporus ruber. J. Am. Chem. Soc., 1969. 91, 1263-1264.
    • (1969) J. Am. Chem. Soc , vol.91 , pp. 1263-1264
    • Wasserman, H.H.1    Rodgers, G.C.2    Keith, D.D.3
  • 182
    • 39149120828 scopus 로고    scopus 로고
    • Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis
    • Mo, S.; Sydor, P. K.; Corre, C.; Alhamadsheh, M. M.; Stanley, A. E.; Haynes, S. W.; Song, L.; Reynolds, K. A.; Challis, G. L., Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis. Chem. Biol., 2008. 15, 137-148.
    • (2008) Chem. Biol , vol.15 , pp. 137-148
    • Mo, S.1    Sydor, P.K.2    Corre, C.3    Alhamadsheh, M.M.4    Stanley, A.E.5    Haynes, S.W.6    Song, L.7    Reynolds, K.A.8    Challis, G.L.9
  • 183
    • 49049085250 scopus 로고    scopus 로고
    • A prodigiosin from the roseophilin producer Streptomyces griseoviridis
    • Kawasaki, T.; Sakurai, F.; Hayakawa, Y., A prodigiosin from the roseophilin producer Streptomyces griseoviridis. J. Nat. Prod., 2008. 71, 1265-1267.
    • (2008) J. Nat. Prod , vol.71 , pp. 1265-1267
    • Kawasaki, T.1    Sakurai, F.2    Hayakawa, Y.3
  • 184
    • 70349935149 scopus 로고    scopus 로고
    • Development of a merged conjugate addition/oxidative coupling sequence. application to the enantioselective total synthesis of metacycloprodigiosin and prodigiosin R1
    • Clift, M. D.; Thomson, R. J., Development of a merged conjugate addition/oxidative coupling sequence. application to the enantioselective total synthesis of metacycloprodigiosin and prodigiosin R1. J. Am. Chem. Soc., 2009. 131, 14579-14583.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 14579-14583
    • Clift, M.D.1    Thomson, R.J.2
  • 185
    • 79951521145 scopus 로고    scopus 로고
    • Enantioselective total synthesis and confirmation of the absolute and relative stereochemistry of streptorubin B
    • Hu, D. X.; Clift, M. D.; Lazarski, K. E.; Thomson, R. J., Enantioselective total synthesis and confirmation of the absolute and relative stereochemistry of streptorubin B. J. Am. Chem. Soc., 2011. 133, 1799-1804.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 1799-1804
    • Hu, D.X.1    Clift, M.D.2    Lazarski, K.E.3    Thomson, R.J.4
  • 186
    • 0038729533 scopus 로고    scopus 로고
    • Direct catalytic asymmetric enolexo aldolizations
    • Pidathala, C.; Hoang, L.; Vignola, N.; List, B., Direct catalytic asymmetric enolexo aldolizations. J. Am. Chem. Soc., 2003. 42, 2785-2788.
    • (2003) J. Am. Chem. Soc , vol.42 , pp. 2785-2788
    • Pidathala, C.1    Hoang, L.2    Vignola, N.3    List, B.4
  • 187
    • 33847065544 scopus 로고    scopus 로고
    • Synthesis of aromatic aldehydes by organocatalytic 4+2 and 3+3 cycloaddition of alpha, beta-unsaturated aldehydes
    • Hong, B.-C.; Tseng, H.-C.; Chen, S.-H., Synthesis of aromatic aldehydes by organocatalytic 4+2 and 3+3 cycloaddition of alpha, beta-unsaturated aldehydes. Tetrahedron, 2007. 63, 2840-2850.
    • (2007) Tetrahedron , vol.63 , pp. 2840-2850
    • Hong, B.-C.1    Tseng, H.-C.2    Chen, S.-H.3
  • 190
    • 80051722795 scopus 로고    scopus 로고
    • Total synthesis of (+)-Przewalskin B
    • Zhuo, X. T.; Xiang, K.; Zhang, F. M.; Tu, Y. Q., Total synthesis of (+)-Przewalskin B. J. Org. Chem., 2011. 76, 6918-6924.
    • (2011) J. Org. Chem , vol.76 , pp. 6918-6924
    • Zhuo, X.T.1    Xiang, K.2    Zhang, F.M.3    Tu, Y.Q.4
  • 191
    • 0034723387 scopus 로고    scopus 로고
    • Chloptosin, an apoptosis-inducing dimeric cyclohexapeptide produced by Streptomyces
    • Umezawa, K.; Ikeda, Y.; Uchihata, Y.; Naganawa, H.; Kondo, S., Chloptosin, an apoptosis-inducing dimeric cyclohexapeptide produced by Streptomyces. J. Org. Chem., 2000. 65, 459-463.
    • (2000) J. Org. Chem , vol.65 , pp. 459-463
    • Umezawa, K.1    Ikeda, Y.2    Uchihata, Y.3    Naganawa, H.4    Kondo, S.5
  • 192
    • 0032538764 scopus 로고    scopus 로고
    • Studies in the total synthesis of himastatin: A revision of the stereochemical assignment
    • Kamenecka, T. M.; Danishefsky, S. J., Studies in the total synthesis of himastatin: A revision of the stereochemical assignment. Angew. Chem. Int. Ed., 1998. 37, 2993-2995.
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 2993-2995
    • Kamenecka, T.M.1    Danishefsky, S.J.2
  • 193
    • 0007002833 scopus 로고    scopus 로고
    • Total synthesis of himastatin: Confirmation of the revised stereostructure
    • Kamenecka, T. M.; Danishefsky, S. J., Total synthesis of himastatin: Confirmation of the revised stereostructure. Angew. Chem. Int. Ed., 1998. 37, 2995-2998.
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 2995-2998
    • Kamenecka, T.M.1    Danishefsky, S.J.2
  • 194
    • 0035808356 scopus 로고    scopus 로고
    • Discovery through total synthesis: A retrospective on the himastatin problem
    • Kamenecka, T. M.; Danishefsky, S. J., Discovery through total synthesis: A retrospective on the himastatin problem. Chem. Eur. J., 2001. 7, 41-63.
    • (2001) Chem. Eur. J , vol.7 , pp. 41-63
    • Kamenecka, T.M.1    Danishefsky, S.J.2
  • 196
    • 33751560440 scopus 로고    scopus 로고
    • A convenient enzymatic synthesis of Lhalotryptophans
    • Goss, R. J. M.; Newill, P. L. A., A convenient enzymatic synthesis of Lhalotryptophans. Chem. Commun., 2006, 4924-4925.
    • (2006) Chem. Commun , pp. 4924-4925
    • Goss, R.J.M.1    Newill, P.L.A.2
  • 197
    • 48649108819 scopus 로고    scopus 로고
    • A convenient one-step synthesis of L-aminotryptophans and improved synthesis of 5-fluorotryptophan
    • Winn, M.; Roy, A. D.; Grueschow, S.; Parameswaran, R. S.; Goss, R. J. M., A convenient one-step synthesis of L-aminotryptophans and improved synthesis of 5-fluorotryptophan. Bioorg. Med. Chem. Lett., 2008. 18, 4508-4510.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 4508-4510
    • Winn, M.1    Roy, A.D.2    Grueschow, S.3    Parameswaran, R.S.4    Goss, R.J.M.5
  • 198
    • 79958119868 scopus 로고    scopus 로고
    • Enantioselective Route to α-Silyl-α-keto Esters by Organocatalyzed regioselective Michael addition of methyl ketones to a (silylmethylene)malonate and their use in natural product synthesis
    • Ghosh, S.; Chowdhury, R., Enantioselective Route to α-Silyl-α-keto Esters by Organocatalyzed regioselective Michael addition of methyl ketones to a (silylmethylene)malonate and their use in natural product synthesis. Synthesis., 2011. 2011, 1936-1945.
    • (2011) Synthesis , vol.2011 , pp. 1936-1945
    • Ghosh, S.1    Chowdhury, R.2
  • 199
    • 0001275805 scopus 로고    scopus 로고
    • Desymmetrization of 3-dimethyl(phenyl)silyl glutaric anhydride with Evans' oxazolidinone: An application to stereocontrolled synthesis of the antifungal agent (+)-preussin
    • Verma, R.; Ghosh, S. K., Desymmetrization of 3-dimethyl(phenyl)silyl glutaric anhydride with Evans' oxazolidinone: an application to stereocontrolled synthesis of the antifungal agent (+)-preussin. J. Chem. Soc.-PT1, 1999, 265-270.
    • (1999) J. Chem. Soc.-PT1 , pp. 265-270
    • Verma, R.1    Ghosh, S.K.2
  • 200
    • 37049066736 scopus 로고
    • Total syntheses of natural (+)-(4R,6R)-4-hydroxy-6-pentylvalerolactone and of (-)-(6r)-massoialactone
    • Bennett, F.; Knight, D. W.; Fenton, G., Total syntheses of natural (+)-(4R,6R)-4-hydroxy-6-pentylvalerolactone and of (-)-(6r)-massoialactone. J. Chem. Soc.-PT1, 1991, 1543-1547.
    • (1991) J. Chem. Soc.-PT1 , pp. 1543-1547
    • Bennett, F.1    Knight, D.W.2    Fenton, G.3
  • 201
    • 0029978168 scopus 로고    scopus 로고
    • Asymmetric synthesis of 5-hexadecanolide, pheromone of the queen of the Oriental hornet, Vespa orientalis
    • Raina, S.; Singh, V. K., Asymmetric synthesis of 5-hexadecanolide, pheromone of the queen of the Oriental hornet, Vespa orientalis. Tetrahedron, 1996. 52, 4479-4484.
    • (1996) Tetrahedron , vol.52 , pp. 4479-4484
    • Raina, S.1    Singh, V.K.2
  • 202
    • 0033533447 scopus 로고    scopus 로고
    • A stereoselective synthesis of (-)-tetrahydrolipstatin
    • Ghosh, A. K.; Liu, C. F., A stereoselective synthesis of (-)-tetrahydrolipstatin. Chem. Commun., 1999, 1743-1744.
    • (1999) Chem. Commun , pp. 1743-1744
    • Ghosh, A.K.1    Liu, C.F.2
  • 203
    • 0034812506 scopus 로고    scopus 로고
    • Amino acid catalyzed direct asymmetric aldol reactions: A bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions
    • Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F., Amino acid catalyzed direct asymmetric aldol reactions: A bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. J. Am. Chem. Soc., 2001. 123, 5260-5267.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 5260-5267
    • Sakthivel, K.1    Notz, W.2    Bui, T.3    Barbas, C.F.4
  • 204
    • 4143114533 scopus 로고    scopus 로고
    • Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-Alder reactions
    • Notz, W.; Tanaka, F.; Barbas, C. F., Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-Alder reactions. Acc. Chem. Res., 2004. 37, 580-591.
    • (2004) Acc. Chem. Res , vol.37 , pp. 580-591
    • Notz, W.1    Tanaka, F.2    Barbas, C.F.3
  • 206
    • 53849146010 scopus 로고    scopus 로고
    • Proline-mediated enantioselective construction of tetrahydropyridines via a cascade Mannich-Type/Intramolecular Cyclization reaction
    • Han, R.-G.; Wang, Y.; Li, Y.-Y.; Xu, P.-F., Proline-mediated enantioselective construction of tetrahydropyridines via a cascade Mannich-Type/Intramolecular Cyclization reaction. Adv. Synth. Cat.,2008. 350, 1474-1478.
    • (2008) Adv. Synth. Cat , vol.350 , pp. 1474-1478
    • Han, R.-G.1    Wang, Y.2    Li, Y.-Y.3    Xu, P.-F.4
  • 207
    • 0033582569 scopus 로고    scopus 로고
    • Asymmetric syntheses of N-Boc 2-substituted pyrrolidines and piperidines by intramolecular cyclization
    • Serino, C.; Stehle, N.; Park, Y. S.; Florio, S.; Beak, P., Asymmetric syntheses of N-Boc 2-substituted pyrrolidines and piperidines by intramolecular cyclization. J. Org. Chem., 1999. 64, 1160-1165.
    • (1999) J. Org. Chem , vol.64 , pp. 1160-1165
    • Serino, C.1    Stehle, N.2    Park, Y.S.3    Florio, S.4    Beak, P.5
  • 208
    • 66149176807 scopus 로고    scopus 로고
    • One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction
    • Chen, Y.; Zhong, C.; Petersen, J. L.; Akhmedov, N. G.; Shi, X., One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction. Org. Lett. 2009. 11, 2333-2336.
    • (2009) Org. Lett , vol.11 , pp. 2333-2336
    • Chen, Y.1    Zhong, C.2    Petersen, J.L.3    Akhmedov, N.G.4    Shi, X.5
  • 209
    • 80054765281 scopus 로고    scopus 로고
    • Asymmetric organocatalytic intramolecular aza-Michael addition of enone carbamates: Catalytic enantioselective access to functionalized 2-substituted piperidines
    • Liu, J.-D.; Chen, Y.-C.; Zhang, G.-B.; Li, Z.-Q.; Chen, P.; Du, J.-Y.; Tu, Y.-Q.; Fan, C.-A., Asymmetric organocatalytic intramolecular aza-Michael addition of enone carbamates: catalytic enantioselective access to functionalized 2-substituted piperidines. Adv. Synth. Cat., 2011. 353, 2721-2730.
    • (2011) Adv. Synth. Cat , vol.353 , pp. 2721-2730
    • Liu, J.-D.1    Chen, Y.-C.2    Zhang, G.-B.3    Li, Z.-Q.4    Chen, P.5    Du, J.-Y.6    Tu, Y.-Q.7    Fan, C.-A.8
  • 210
    • 33745715054 scopus 로고    scopus 로고
    • Modern strategies in organic catalysis: The advent and development of iminium activation
    • Lelais, G.; MacMillan, D. W. C., Modern strategies in organic catalysis: The advent and development of iminium activation. Aldrich. Acta 2006. 39, 79-87.
    • (2006) Aldrich. Acta , vol.39 , pp. 79-87
    • Lelais, G.1    Macmillan, D.W.C.2
  • 212
    • 70249087729 scopus 로고    scopus 로고
    • The organocatalytic addition of bis(arylsulfonyl)methane to α,b-unsaturated aldehydes and the synthesis of optically-enriched 3-methyl-alkanols
    • Ruano, J. L. G.; Marcos, V.; Aleman, J., The organocatalytic addition of bis(arylsulfonyl)methane to α,b-unsaturated aldehydes and the synthesis of optically-enriched 3-methyl-alkanols. Chem. Commun., 2009, 4435-4437.
    • (2009) Chem. Commun , pp. 4435-4437
    • Ruano, J.L.G.1    Marcos, V.2    Aleman, J.3
  • 213
    • 70350512581 scopus 로고    scopus 로고
    • Formal highly enantioselective organocatalytic addition of alkyl anions to α,b -unsaturated aldehydes: Application to the synthesis of isotope-enantiomers
    • Alba, A. N.; Companyo, X.; Moyano, A.; Rios, R., Formal highly enantioselective organocatalytic addition of alkyl anions to α,b -unsaturated aldehydes: application to the synthesis of isotope-enantiomers. Chem. Eur. J., 2009. 15, 11095-11099.
    • (2009) Chem. Eur. J , vol.15 , pp. 11095-11099
    • Alba, A.N.1    Companyo, X.2    Moyano, A.3    Rios, R.4
  • 214
    • 72949111039 scopus 로고    scopus 로고
    • Catalytic conjugate additions of geminal bis(sulfone)s: Expanding the chemistry of sulfones as simple alkyl anion equivalents
    • Landa, A.; Puente, A.; Santos, J. I.; Vera, S.; Oiarbide, M.; Palomo, C., Catalytic conjugate additions of geminal bis(sulfone)s: expanding the chemistry of sulfones as simple alkyl anion equivalents. Chem. Eur. J., 2009. 15, 11954-11962.
    • (2009) Chem. Eur. J , vol.15 , pp. 11954-11962
    • Landa, A.1    Puente, A.2    Santos, J.I.3    Vera, S.4    Oiarbide, M.5    Palomo, C.6
  • 215
    • 78651247556 scopus 로고    scopus 로고
    • Catalytic asymmetric michael reactions of α,b -unsaturated ketones with sulfonyl-containing nucleophiles: Chiral synthesis of (R)-muscone and (S)-celery ketone
    • Sun, X. M.; Yu, F.; Ye, T. T.; Liang, X. M.; Ye, J. X., catalytic asymmetric michael reactions of α,b -unsaturated ketones with sulfonyl-containing nucleophiles: chiral synthesis of (R)-muscone and (S)-celery ketone. Chem. Eur. J., 2011. 17, 430-434.
    • (2011) Chem. Eur. J , vol.17 , pp. 430-434
    • Sun, X.M.1    Yu, F.2    Ye, T.T.3    Liang, X.M.4    Ye, J.X.5
  • 216
    • 79959681231 scopus 로고    scopus 로고
    • Catalytic enantioselective Henry reactions of isatins: Application in the concise synthesis of (S)-(-)-Spirobrassinin
    • Liu, L.; Zhang, S. L.; Xue, F.; Lou, G. S.; Zhang, H. Y.; Ma, S. C.; Duan, W. H.; Wang, W., Catalytic enantioselective Henry reactions of isatins: application in the concise synthesis of (S)-(-)-Spirobrassinin. Chem. Eur. J., 2011. 17, 7791-7795.
    • (2011) Chem. Eur. J , vol.17 , pp. 7791-7795
    • Liu, L.1    Zhang, S.L.2    Xue, F.3    Lou, G.S.4    Zhang, H.Y.5    Ma, S.C.6    Duan, W.H.7    Wang, W.8
  • 217
    • 79958090302 scopus 로고    scopus 로고
    • Organocatalytic enantioselective approach to the synthesis of Verbalactone and (R)-Massoialactone
    • Harbindu, A.; Kumar, P., Organocatalytic enantioselective approach to the synthesis of Verbalactone and (R)-Massoialactone. Synthesis,2011, 1954-1959.
    • (2011) Synthesis , pp. 1954-1959
    • Harbindu, A.1    Kumar, P.2
  • 218
    • 82255192248 scopus 로고    scopus 로고
    • An organocatalytic route to the synthesis of (6S)-5,6-dihydro-6- (2R)-2-hydroxy-6-phenylhexyl -2H-pyran-2-one and ravensara lactones
    • Dwivedi, N.; Tripathi, D.; Kumar, P., An organocatalytic route to the synthesis of (6S)-5,6-dihydro-6- (2R)-2-hydroxy-6-phenylhexyl -2H-pyran-2-one and ravensara lactones. Tetrahedron-Asymmetry 2011. 22, 1749-1756.
    • (2011) Tetrahedron-Asymmetry , vol.22 , pp. 1749-1756
    • Dwivedi, N.1    Tripathi, D.2    Kumar, P.3
  • 220
    • 82455219460 scopus 로고    scopus 로고
    • A unified strategy for the asymmetric total syntheses of Diversonol and Lachnone C
    • Brohmer, M. C.; Bourcet, E.; Nieger, M.; Brase, S., A unified strategy for the asymmetric total syntheses of Diversonol and Lachnone C. Chem. Eur. J., 2011. 17, 13706-13711.
    • (2011) Chem. Eur. J , vol.17 , pp. 13706-13711
    • Brohmer, M.C.1    Bourcet, E.2    Nieger, M.3    Brase, S.4
  • 221
    • 82455192842 scopus 로고    scopus 로고
    • Enantioselective Syntheses of Corynanthe Alkaloids by Chiral Bronsted Acid and Palladium Catalysis
    • Wanner, M. J.; Claveau, E.; van Maarseveen, J. H.; Hiemstra, H., Enantioselective Syntheses of Corynanthe Alkaloids by Chiral Bronsted Acid and Palladium Catalysis. Chem. Eur. J., 2011. 17, 13680-13683.
    • (2011) Chem. Eur. J , vol.17 , pp. 13680-13683
    • Wanner, M.J.1    Claveau, E.2    van Maarseveen, J.H.3    Hiemstra, H.4
  • 222
    • 82455192855 scopus 로고    scopus 로고
    • A Stereodivergent Strategy for the Preparation of Corynantheine and Ipecac Alkaloids, Their Epimers, and Analogues: Efficient Total Synthesis of (-)-Dihydrocorynantheol, (-)-Corynantheol, (-)-Protoemetinol, (-)-Corynantheal, (-)-Protoemetine, and Related Natural and Nonnatural Compounds
    • Zhang, W.; Bah, J.; Wohlfarth, A.; Franzen, J., A Stereodivergent Strategy for the Preparation of Corynantheine and Ipecac Alkaloids, Their Epimers, and Analogues: Efficient Total Synthesis of (-)-Dihydrocorynantheol, (-)-Corynantheol, (-)-Protoemetinol, (-)-Corynantheal, (-)-Protoemetine, and Related Natural and Nonnatural Compounds. Chem. Eur. J., 2011. 17, 13814-13824.
    • (2011) Chem. Eur. J , vol.17 , pp. 13814-13824
    • Zhang, W.1    Bah, J.2    Wohlfarth, A.3    Franzen, J.4
  • 223
    • 84857929619 scopus 로고    scopus 로고
    • Total synthesis of the Galbulimima alkaloid (-)-GB17
    • Larson, R. T.; Clift, M. D.; Thomson, R. J., Total synthesis of the Galbulimima alkaloid (-)-GB17. J. Am. Chem. Soc., 2012. 51, 2481-2484.
    • (2012) J. Am. Chem. Soc , vol.51 , pp. 2481-2484
    • Larson, R.T.1    Clift, M.D.2    Thomson, R.J.3
  • 225
    • 84857072457 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (+)-galbulin via organocatalytic domino Michael-Michael-aldol condensation
    • Hong, B.-C.; Hsu, C.-S.; Lee, G.-H., Enantioselective total synthesis of (+)-galbulin via organocatalytic domino Michael-Michael-aldol condensation. Chem. Commun., 2012. 48, 2385-2387.
    • (2012) Chem. Commun , vol.48 , pp. 2385-2387
    • Hong, B.-C.1    Hsu, C.-S.2    Lee, G.-H.3
  • 226
    • 84855185340 scopus 로고    scopus 로고
    • Concise Total Synthesis of Dihydrocorynanthenol, Protoemetinol, Protoemetine, 3-epi-Protoemetinol and Emetine
    • Lin, S.; Deiana, L.; Tseggai, A.; Cordova, A., Concise Total Synthesis of Dihydrocorynanthenol, Protoemetinol, Protoemetine, 3-epi-Protoemetinol and Emetine. Eur. J. Org. Chem. 2012, 398-408.
    • (2012) Eur. J. Org. Chem , pp. 398-408
    • Lin, S.1    Deiana, L.2    Tseggai, A.3    Cordova, A.4
  • 228
    • 77952328004 scopus 로고    scopus 로고
    • Asymmetric, protecting-group-free total synthesis of (-)-Englerin A
    • Zhou, Q. H.; Chen, X. F.; Ma, D. W., Asymmetric, protecting-group-free total synthesis of (-)-Englerin A. Angew. Chem. Int. Ed., 2010. 49, 3513-3516.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 3513-3516
    • Zhou, Q.H.1    Chen, X.F.2    Ma, D.W.3
  • 229
    • 77952397509 scopus 로고    scopus 로고
    • Enantioselective synthesis of (-)-Englerins A and B
    • Molawi, K.; Delpont, N.; Echavarren, A. M., Enantioselective synthesis of (-)-Englerins A and B. Angew. Chem. Int. Ed., 2010. 49, 3517-3519.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 3517-3519
    • Molawi, K.1    Delpont, N.2    Echavarren, A.M.3
  • 231
    • 77955683809 scopus 로고    scopus 로고
    • Enantioselective formal synthesis of (-)-Englerin A via a Rh-catalyzed 4+3 cycloaddition reaction
    • Xu, J.; Caro-Diaz, E. J. E.; Theodorakis, E. A., Enantioselective formal synthesis of (-)-Englerin A via a Rh-catalyzed 4+3 cycloaddition reaction. Org. Lett., 2010. 12, 3708-3711.
    • (2010) Org. Lett , vol.12 , pp. 3708-3711
    • Xu, J.1    Caro-Diaz, E.J.E.2    Theodorakis, E.A.3
  • 232
    • 79953207640 scopus 로고    scopus 로고
    • Concise approach to the core of englerin A via an organocatalytic 4+3 cycloaddition reaction
    • Sun, B. F.; Wang, C. L.; Ding, R.; Xu, J. Y.; Lin, G. Q., Concise approach to the core of englerin A via an organocatalytic 4+3 cycloaddition reaction. Tetrahedron Lett., 2011. 52, 2155-2158.
    • (2011) Tetrahedron Lett , vol.52 , pp. 2155-2158
    • Sun, B.F.1    Wang, C.L.2    Ding, R.3    Xu, J.Y.4    Lin, G.Q.5
  • 233
    • 79952094960 scopus 로고    scopus 로고
    • Chemical Synthesis and Biological Evaluation of the Englerin Analogues
    • Chan, K. P.; Chen, D. Y. K., Chemical Synthesis and Biological Evaluation of the Englerin Analogues. Chem. Med. Chem., 2011. 6, 420-423.
    • (2011) Chem. Med. Chem , vol.6 , pp. 420-423
    • Chan, K.P.1    Chen, D.Y.K.2
  • 236
    • 79955461496 scopus 로고    scopus 로고
    • A Brief Synthesis of (-)-Englerin A
    • Li, Z. W.; Nakashige, M.; Chain, W. J., A Brief Synthesis of (-)-Englerin A. J. Am. Chem. Soc., 2011. 133, 6553-6556.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 6553-6556
    • Li, Z.W.1    Nakashige, M.2    Chain, W.J.3
  • 238
    • 84855860684 scopus 로고    scopus 로고
    • Concise formal synthesis of (+)-Englerin A and total synthesis of (-)-Orientalol F: Establishment of the stereochemistry of the organocatalytic 4+3 -cycloaddition Reaction
    • Wang, C.-L.; Sun, B.-F.; Chen, S.-G.; Ding, R.; Lin, G.-Q.; Xu, J.-Y.; Shang, Y.-J., Concise formal synthesis of (+)-Englerin A and total synthesis of (-)-Orientalol F: establishment of the stereochemistry of the organocatalytic 4+3 -cycloaddition Reaction. Synlett, 2012, 263-266.
    • (2012) Synlett , pp. 263-266
    • Wang, C.-L.1    Sun, B.-F.2    Chen, S.-G.3    Ding, R.4    Lin, G.-Q.5    Xu, J.-Y.6    Shang, Y.-J.7
  • 239
    • 84860613439 scopus 로고    scopus 로고
    • An Expeditious total synthesis of both diastereoisomeric lipid dihydroxytetrahydrofurans from Notheia anomala
    • Roy, S.; Spilling, C. D., An Expeditious total synthesis of both diastereoisomeric lipid dihydroxytetrahydrofurans from Notheia anomala. Org. Lett., 2012. 14, 2230-2233.
    • (2012) Org. Lett , vol.14 , pp. 2230-2233
    • Roy, S.1    Spilling, C.D.2
  • 240
    • 84860820948 scopus 로고    scopus 로고
    • Stereocontrolled Synthesis of Vicinal Diamines by Organocatalytic Asymmetric Mannich Reaction of N-Protected Aminoacetaldehydes: Formal Synthesis of (-)-Agelastatin A
    • Kano, T.; Sakamoto, R.; Akakura, M.; Maruoka, K., Stereocontrolled Synthesis of Vicinal Diamines by Organocatalytic Asymmetric Mannich Reaction of N-Protected Aminoacetaldehydes: Formal Synthesis of (-)-Agelastatin A. J. Am. Chem. Soc 2012. 134, 7516-7520.
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 7516-7520
    • Kano, T.1    Sakamoto, R.2    Akakura, M.3    Maruoka, K.4
  • 241
    • 34547953030 scopus 로고    scopus 로고
    • Synthesis of (-)-agelastatin a by 3.3 sigmatropic rearrangement of allyl cyanate
    • Ichikawa, Y.; Yamaoka, T.; Nakano, K.; Kotsuki, H., Synthesis of (-)-agelastatin a by 3.3 sigmatropic rearrangement of allyl cyanate. Org. Lett. 2007. 9, 2989-2992.
    • (2007) Org. Lett , vol.9 , pp. 2989-2992
    • Ichikawa, Y.1    Yamaoka, T.2    Nakano, K.3    Kotsuki, H.4
  • 242
    • 84862907571 scopus 로고    scopus 로고
    • Corestructure-oriented asymmetric organocatalytic substitution of 3-hydroxyoxindoles: Application in the enantioselective total synthesis of (+)-folicanthine
    • Guo, C.; Song, J.; Huang, J. Z.; Chen, P. H.; Luo, S. W.; Gong, L. Z., Corestructure-oriented asymmetric organocatalytic substitution of 3-hydroxyoxindoles: application in the enantioselective total synthesis of (+)-folicanthine. Angew Chem Int Ed Engl 2012. 51, 1046-1050.
    • (2012) Angew Chem Int Ed Engl , vol.51 , pp. 1046-1050
    • Guo, C.1    Song, J.2    Huang, J.Z.3    Chen, P.H.4    Luo, S.W.5    Gong, L.Z.6
  • 243
    • 84857565366 scopus 로고    scopus 로고
    • Synthesis of (+)-L-733,060, (+)-CP-99,994 and (2S,3R)-3-hydroxypipecolic acid: Application of an organocatalytic direct vinylogous aldol reaction
    • Pansare, S. V.; Paul, E. K., Synthesis of (+)-L-733,060, (+)-CP-99,994 and (2S,3R)-3-hydroxypipecolic acid: Application of an organocatalytic direct vinylogous aldol reaction. Org. & Biomol. Chem., 2012. 10, 2119-2125.
    • (2012) Org. & Biomol. Chem , vol.10 , pp. 2119-2125
    • Pansare, S.V.1    Paul, E.K.2
  • 244
    • 77749309286 scopus 로고    scopus 로고
    • Asymmetric direct vinylogous aldol reaction of furanone derivatives catalyzed by an axially chiral guanidine base
    • Ube, H.; Shimada, N.; Terada, M., Asymmetric direct vinylogous aldol reaction of furanone derivatives catalyzed by an axially chiral guanidine base. Angew. Chem. Int. Ed., 2010. 49, 1858-1861.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 1858-1861
    • Ube, H.1    Shimada, N.2    Terada, M.3
  • 245
    • 78650490188 scopus 로고    scopus 로고
    • Organocatalytic asymmetric direct vinylogous aldol reactions of gamma-crotonolactone with aromatic aldehydes
    • Pansare, S. V.; Paul, E. K., Organocatalytic asymmetric direct vinylogous aldol reactions of gamma-crotonolactone with aromatic aldehydes. Chem. Commun. 2011. 47, 1027-1029.
    • (2011) Chem. Commun , vol.47 , pp. 1027-1029
    • Pansare, S.V.1    Paul, E.K.2


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