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Volumn 14, Issue 4, 2010, Pages 414-424

Multi-component reactions using indium(III) salts

Author keywords

[No Author keywords available]

Indexed keywords

INDIUM COMPOUNDS;

EID: 77954364149     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527210790231900     Document Type: Article
Times cited : (21)

References (110)
  • 1
    • 2542509173 scopus 로고    scopus 로고
    • Multicomponent Reactions with Isicyanides
    • Domling, A.; Ugi, I. Multicomponent Reactions with Isicyanides. Angew. Chem. Int. Ed. 2000, 39, 3168-3210.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3168-3210
    • Domling, A.1    Ugi, I.2
  • 2
    • 17144366282 scopus 로고    scopus 로고
    • Asymmetric Multicomponent Reactions (AMCRs): The New Frontier
    • Ramon, D.J.; Yus, M. Asymmetric Multicomponent Reactions (AMCRs): The New Frontier. Angew. Chem. Int. Ed. 2005, 44, 1602.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1602
    • Ramon, D.J.1    Yus, M.2
  • 3
    • 1042275565 scopus 로고    scopus 로고
    • Pillai Indium-and gallium-mediated carbon-carbon bond-forming reactions in organic synthesis
    • V. Nair.; S. Ros.; Jayan, C.N.; Bindu, S. Pillai Indium-and gallium-mediated carbon-carbon bond-forming reactions in organic synthesis. Tetrahedron 2004, 60, 1959.
    • (2004) Tetrahedron , vol.60 , pp. 1959
    • Nair, V.1    Ros, S.2    Jayan, C.N.3    Bindu, S.4
  • 4
    • 5144230869 scopus 로고    scopus 로고
    • A novel atom-transfer cyclisation catalysed by indium metal in halogenated solvents
    • Bhatti, N.H.; Salter, M..M. A novel atom-transfer cyclisation catalysed by indium metal in halogenated solvents. Tetrahedron Lett. 2004, 45, 8379.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 8379
    • Bhatti, N.H.1    Salter, M..M.2
  • 5
    • 0022154721 scopus 로고
    • Differential effects of photoactive furanyl compounds on virus functions
    • Hudson, J.B.; Graham, E.A.; Chan, G.C.; Towers, G.H.N. Differential effects of photoactive furanyl compounds on virus functions. Photocehm. Photobiol. 1985, 42, 523.
    • (1985) Photocehm. Photobiol. , vol.42 , pp. 523
    • Hudson, J.B.1    Graham, E.A.2    Chan, G.C.3    Towers, G.H.N.4
  • 6
    • 0022385516 scopus 로고
    • Mutagenic activities of dictamnine and y-fagarine from Dictamni Radicis Cortex (Rutaceae)
    • Mizuta, M.; Kannamori, H. Mutagenic activities of dictamnine and y-fagarine from Dictamni Radicis Cortex (Rutaceae). Mutat. Res. 1985, 144, 221.
    • (1985) Mutat. Res. , vol.144 , pp. 221
    • Mizuta, M.1    Kannamori, H.2
  • 7
    • 34248143433 scopus 로고    scopus 로고
    • First detection of the plasmid-mediated quinolone resistance determinant qnrA in Enterobacteriaceae clinical isolates in Japan
    • Saga, T.; Akasaka, T.; Takase, H.; Tanaka, M.; Sato, K.; Kaku, V. First detection of the plasmid-mediated quinolone resistance determinant qnrA in Enterobacteriaceae clinical isolates in Japan. Int. J. Antimicrob. Agents 2007, 29, 738.
    • (2007) Int. J. Antimicrob. Agents , vol.29 , pp. 738
    • Saga, T.1    Akasaka, T.2    Takase, H.3    Tanaka, M.4    Sato, K.5    Kaku, V.6
  • 8
    • 0029999886 scopus 로고    scopus 로고
    • HIV Inhibitory Natural Products 26.1 Quinoline alkaloids from euodia roxburghiana
    • McCommick, J.L.; McTee, T.C.; Cardellina, J.H.; Boyd, M.R. HIV Inhibitory Natural Products. 26.1 Quinoline alkaloids from euodia roxburghiana. J. Nat. Prod. 1996, 59, 469.
    • (1996) J. Nat. Prod. , vol.59 , pp. 469
    • McCommick, J.L.1    McTee, T.C.2    Cardellina, J.H.3    Boyd, M.R.4
  • 9
    • 0037204923 scopus 로고    scopus 로고
    • InCl3-Catalyzed Domino Reaction of Aromatic Amines with Cyclic Enol Ethers in Water: A Highly Efficient Synthesis of New 1,2,3,4-Tetrahydroquinoline Derivatives
    • Zhang, J.; Li, C-J. InCl3-Catalyzed Domino Reaction of Aromatic Amines with Cyclic Enol Ethers in Water: A Highly Efficient Synthesis of New 1,2,3,4-Tetrahydroquinoline Derivatives. J. Org. Chem. 2002, 67, 3969.
    • (2002) J. Org. Chem. , vol.67 , pp. 3969
    • Zhang, J.1    Li, C.-J.2
  • 11
    • 15544363267 scopus 로고    scopus 로고
    • 3 as an efficient catalyst for intramolecular imino Diels-Alder reactions: Synthesis of tetrahydrochromano quino lines
    • 3 as an efficient catalyst for intramolecular imino Diels-Alder reactions: Synthesis of tetrahydrochromano quino lines. Arkivoc 2005, XI, 6.
    • (2005) Arkivoc , vol.11 , pp. 6
    • Elamparuthi, E.1    Anniyappan, M.2    Muralidharan, D.3    Perumal, P.T.4
  • 12
    • 0034699215 scopus 로고    scopus 로고
    • Indium triflate: a new catalyst for (4 + 2)-cycloaddition of chromone Schiffs bases
    • Gadhwal, S.; Sandhu, J.S. Indium triflate: a new catalyst for (4 + 2)-cycloaddition of chromone Schiffs bases. J. Chem. Soc. Perkin Trans. 1 2000, 16, 2827.
    • (2000) J. Chem. Soc. Perkin Trans. 1 , vol.16 , pp. 2827
    • Gadhwal, S.1    Sandhu, J.S.2
  • 14
    • 33748752227 scopus 로고    scopus 로고
    • Rapid synthesis of tetrahydroquinolines by indium trichloride catalyzed mono-and bis-intramolecular imino Diels-Alder reactions
    • Rathna, R.S.M.D.; Jayashankaran, J.; Ramesh, R.; Raghunathan, R. Rapid synthesis of tetrahydroquinolines by indium trichloride catalyzed mono-and bis-intramolecular imino Diels-Alder reactions. Tetrahedron Lett. 2006, 47, 7571.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 7571
    • Rathna, R.S.M.D.1    Jayashankaran, J.2    Ramesh, R.3    Raghunathan, R.4
  • 15
    • 34247881744 scopus 로고    scopus 로고
    • Indium trichloride catalyzed one-pot synthesis of indolo[2,1-a]pyrrolo[4',3':2,3]-7a,8,13,13b-tetrahydroquinolines through intramolecular imino Diels-Alder reactions
    • Rathna, R.S.M.D.; Jayashankaran, J.; Raghunathan, R. Indium trichloride catalyzed one-pot synthesis of indolo[2,1-a]pyrrolo[4',3':2,3]-7a,8,13,13b-tetrahydroquinolines through intramolecular imino Diels-Alder reactions. Tetrahedron Lett. 2007, 48, 4139.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4139
    • Rathna, R.S.M.D.1    Jayashankaran, J.2    Raghunathan, R.3
  • 16
    • 25744438736 scopus 로고
    • Scientific Papers of the Institute of Organic and Physical Chemistry, Wroclaw Technical University, Wroclaw, No. 13/8
    • Sliwa, W. Studies on Benzo[h]naphthyridines, Scientific Papers of the Institute of Organic and Physical Chemistry, Wroclaw Technical University, Wroclaw, 1978 No. 13/8.
    • (1978) Studies on Benzo[h]naphthyridines
    • Sliwa, W.1
  • 17
    • 0000585545 scopus 로고    scopus 로고
    • Grazyna Matusiak 1,3-Dipolar cycloaddition reactions of the ylide derived from 6-Phenacyl-benzo[f][1,7]naphthyridinium bromide
    • Grazyna Matusiak 1,3-Dipolar cycloaddition reactions of the ylide derived from 6-Phenacyl-benzo[f][1,7]naphthyridinium bromide. Aust. J. Chem. 1999, 52, 149.
    • (1999) Aust. J. Chem. , vol.52 , pp. 149
  • 18
    • 0001614099 scopus 로고
    • Synthesis and Properties of Methyl-Formyl-and Amino-Diazaphenanthrene
    • Chrzastek, L.; Mianowska, B.; Sliwa, W. Synthesis and Properties of Methyl-, Formyl-and Amino-Diazaphenanthrene. Aust. J. Chem. 1994, 47, 2129.
    • (1994) Aust. J. Chem. , vol.47 , pp. 2129
    • Chrzastek, L.1    Mianowska, B.2    Sliwa, W.3
  • 19
    • 0037751162 scopus 로고    scopus 로고
    • Chemistry and applications of benzonaphthyridines
    • Bachowska, B.; Zujewska, T. Chemistry and applications of benzonaphthyridines. Arkivoc 2001, (vi) 77.
    • (2001) Arkivoc , vol.6 , pp. 77
    • Bachowska, B.1    Zujewska, T.2
  • 20
    • 0037529208 scopus 로고    scopus 로고
    • Dihydropyridine-Based Multicomponent Reactions. Efficient Entry into New Tetrahydroquinoline Systems through Lewis Acid-Catalyzed Formal [4 + 2] Cycloadditions
    • Lavilla, R.; Bernabeu, M.C.; Carranco, I.; Diaz, J. L. Dihydropyridine-Based Multicomponent Reactions. Efficient Entry into New Tetrahydroquinoline Systems through Lewis Acid-Catalyzed Formal [4 + 2] Cycloadditions. Org. Lett. 2003, 5, 717.
    • (2003) Org. Lett. , vol.5 , pp. 717
    • Lavilla, R.1    Bernabeu, M.C.2    Carranco, I.3    Diaz, J.L.4
  • 21
    • 0034676585 scopus 로고    scopus 로고
    • A Diastereoselective Synthesis of 2,4-Disubstituted Piperidines: Scaffolds for Drug Discovery
    • Watson, P.S.; Jiang, B.; Scott, B. A Diastereoselective Synthesis of 2,4-Disubstituted Piperidines: Scaffolds for Drug Discovery. Org. Lett. 2000, 2, 3679.
    • (2000) Org. Lett. , vol.2 , pp. 3679
    • Watson, P.S.1    Jiang, B.2    Scott, B.3
  • 22
    • 34250850717 scopus 로고    scopus 로고
    • Pot, atom and step economic (PASE) synthesis of highly functionalized piperidines: a five-component condensation
    • Clarke, P.A.; Zaytzev, A.V.; Whitewood, A.C. Pot, atom and step economic (PASE) synthesis of highly functionalized piperidines: a five-component condensation. Tetrahedron Lett. 2007, 48, 5209.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 5209
    • Clarke, P.A.1    Zaytzev, A.V.2    Whitewood, A.C.3
  • 23
    • 0033166293 scopus 로고    scopus 로고
    • Indium triflate-an efficient catalyst for hetero Diels-Alder reactions
    • Ali, T.; Chauhan, K.K.; Frost, C.G. Indium triflate-an efficient catalyst for hetero Diels-Alder reactions. Tetrahedron Lett. 1999, 40, 5621.
    • (1999) Tetrahedron Lett , vol.40 , pp. 5621
    • Ali, T.1    Chauhan, K.K.2    Frost, C.G.3
  • 24
    • 0035894174 scopus 로고    scopus 로고
    • The anticancer agent ellipticine on activation by cytochrome P450 forms covalent DNA adducts
    • Stiborová, M.; Bieler, C.A.; Wiessler, M.; Frei, E. The anticancer agent ellipticine on activation by cytochrome P450 forms covalent DNA adducts, Biochem. Pharmacol. 2001, 62, 1675.
    • (2001) Biochem. Pharmacol. , vol.62 , pp. 1675
    • Stiborová, M.1    Bieler, C.A.2    Wiessler, M.3    Frei, E.4
  • 26
    • 0023617219 scopus 로고
    • Multimodal action of antitumor agents on DNA: The ellipticine series
    • Auclair, C. Multimodal action of antitumor agents on DNA: The ellipticine series. Arch. Biochem. Biophys. 1987, 259, 1.
    • (1987) Arch. Biochem. Biophys. , vol.259 , pp. 1
    • Auclair, C.1
  • 27
    • 58849165439 scopus 로고    scopus 로고
    • A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction
    • Gaddam, V.; Nagarajan, R. A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction. Tetrahedron Lett. 2009, 50, 1243.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1243
    • Gaddam, V.1    Nagarajan, R.2
  • 28
    • 67650529102 scopus 로고    scopus 로고
    • An efficient one-pot synthesis of tetrahydrobenzo[a]xanthene-11-one and diazabenzo[a]anthracene-9,11-dione derivatives under solvent free condition
    • and reference cited therein
    • Nandi, G.C.; Samai, S.; Kumar, R.; Singh, M.S. An efficient one-pot synthesis of tetrahydrobenzo[a]xanthene-11-one and diazabenzo[a]anthracene-9,11-dione derivatives under solvent free condition. Tetrahedron 2009, 65, 7129 and reference cited therein.
    • (2009) Tetrahedron , vol.65 , pp. 7129
    • Nandi, G.C.1    Samai, S.2    Kumar, R.3    Singh, M.S.4
  • 29
    • 1542268928 scopus 로고    scopus 로고
    • Indium(III) chloride catalyzed in situ generation of enamines and cyclization with imines: a novel route for synthesis of hexahydroxanthene-9-N-arylamines
    • Anniyappan, M.; Muralidharan, D.; Perumal, P.T.; Vittal, J. J. Indium(III) chloride catalyzed in situ generation of enamines and cyclization with imines: a novel route for synthesis of hexahydroxanthene-9-N-arylamines. Tetrahedron 2004, 60, 2965.
    • (2004) Tetrahedron , vol.60 , pp. 2965
    • Anniyappan, M.1    Muralidharan, D.2    Perumal, P.T.3    Vittal, J.J.4
  • 30
    • 0023836413 scopus 로고
    • Synthesis and antiviral properties of (E)-5-(2-bromovinyl)-2'-deoxycytidine-related compounds
    • Jones, A.S.; Swgers, J.R.; Walker, R.T.; Clercq, E.D. Synthesis and antiviral properties of (E)-5-(2-bromovinyl)-2'-deoxycytidine-related compounds. J. Med. Chem. 1988, 31, 268.
    • (1988) J. Med. Chem. , vol.31 , pp. 268
    • Jones, A.S.1    Swgers, J.R.2    Walker, R.T.3    Clercq, E.D.4
  • 31
    • 0000338765 scopus 로고
    • Brown, J.D. In: Katritzky, A.R.; Rees, C.W. (Eds). Pergamon Press, Oxford
    • Brown, J.D. In: Katritzky, A.R.; Rees, C.W. (Eds) Comprehensive Heterocyclic Chemistry. Pergamon Press, Oxford, 1984, Vol. 3, p. 57.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 57
  • 32
    • 0000430412 scopus 로고
    • Experimental and Clinical Use of Fluorinated Pyrimidines in Cancer Chemotherapy
    • Heidelberger, C.; Ansfield, F.J. Experimental and Clinical Use of Fluorinated Pyrimidines in Cancer Chemotherapy. Cancer Res. 1964, 23, 1226.
    • (1964) Cancer Res. , vol.23 , pp. 1226
    • Heidelberger, C.1    Ansfield, F.J.2
  • 33
    • 0022552064 scopus 로고
    • Chemotherapeutic approaches to the treatment of the acquired immune deficiency syndrome (AIDS)
    • Clercq, E.D. Chemotherapeutic approaches to the treatment of the acquired immune deficiency syndrome (AIDS). J. Med. Chem. 1986, 29, 1561.
    • (1986) J. Med. Chem. , vol.29 , pp. 1561
    • Clercq, E.D.1
  • 34
    • 0023124801 scopus 로고
    • Both 2',3'-dideoxythymidine and its 2',3'-unsaturated derivative (2',3'-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro
    • Baba, M.; Pauvels, R.; Herdwig, P.; Clercq, E.D.; Desmyster, J.; Vandeputte, M.; Both 2',3'-dideoxythymidine and its 2',3'-unsaturated derivative (2',3'-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro. Biochem. Biophys. Res. Commun. 1987, 142, 128.
    • (1987) Biochem. Biophys. Res. Commun. , vol.142 , pp. 128
    • Baba, M.1    Pauvels, R.2    Herdwig, P.3    Clercq, E.D.4    Desmyster, J.5    Vandeputte, M.6
  • 35
    • 0022481507 scopus 로고
    • Potential of bromovinyldeoxyuridine in anticancer chemotherapy
    • Clercq, E.D. Potential of bromovinyldeoxyuridine in anticancer chemotherapy. Anticancer Res. 1986, 6, 549.
    • (1986) Anticancer Res , vol.6 , pp. 549
    • Clercq, E.D.1
  • 36
    • 0000676995 scopus 로고    scopus 로고
    • Reactivity of Thioaldehyde: Cyclization Reaction of 6-Amino-1,3-dimethyl-5-thioformyluracil with Enamines into Pyrido[2,3-d]pyrimidine-2,4-(1H,3H)-diones
    • Hirota, K.; Kubo, K.; Sajiki, H.; Kitade, Y.; Sako, M.; Maki, Y. Reactivity of Thioaldehyde: Cyclization Reaction of 6-Amino-1,3-dimethyl-5-thioformyluracil with Enamines into Pyrido[2,3-d]pyrimidine-2,4-(1H,3H)-diones. J. Org. Chem. 1997, 62, 2999.
    • (1997) J. Org. Chem. , vol.62 , pp. 2999
    • Hirota, K.1    Kubo, K.2    Sajiki, H.3    Kitade, Y.4    Sako, M.5    Maki, Y.6
  • 37
    • 0017296451 scopus 로고
    • Pyrido[2,3-d]pyrimidines. IV. Synthetic studies leading to various oxopyrido[2,3-d]pyrimidines
    • Anderson, G.L.; Shim, J.L.; Brown, A.D. Pyrido[2,3-d]pyrimidines. IV. Synthetic studies leading to various oxopyrido[2,3-d]pyrimidines. J. Org. Chem. 1976, 41, 1095.
    • (1976) J. Org. Chem , vol.41 , pp. 1095
    • Anderson, G.L.1    Shim, J.L.2    Brown, A.D.3
  • 38
    • 0018874182 scopus 로고
    • Synthesis and antitumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine
    • Grivaky, E.M.; Lee, S.; Siyal, C.W.; Duch, D.S.; Nichol, C.A. Synthesis and antitumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine. J. Med. Chem. 1980, 23, 327.
    • (1980) J. Med. Chem. , vol.23 , pp. 327
    • Grivaky, E.M.1    Lee, S.2    Siyal, C.W.3    Duch, D.S.4    Nichol, C.A.5
  • 39
    • 33746763761 scopus 로고    scopus 로고
    • An efficient synthesis of novel pyrano[2,3-d]-and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component dominoreaction
    • Prajapati, D.; Gohain, M. An efficient synthesis of novel pyrano[2,3-d]-and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component dominoreaction. Beilstein J. Org. Chem. 2006, 2, 11.
    • (2006) Beilstein J. Org. Chem. , vol.2 , pp. 11
    • Prajapati, D.1    Gohain, M.2
  • 41
    • 84944049928 scopus 로고
    • Katrizky, A.R.; Rees, C.W. (Eds). Pergamon, Oxford
    • Hepworth, J. In: Katrizky, A.R.; Rees, C.W. (Eds) Comprehensive Heterocyclic Chemistry. Pergamon, Oxford, 1984, Vol. 3, p. 737.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 737
    • Hepworth, J.1
  • 44
    • 0037164634 scopus 로고    scopus 로고
    • Diastereoselective synthesis of cis-fused pyrano and furanobenzopyrans catalyzed by indium trichloride or triphenyl phosphonium perchlorate
    • Anniyappan, M.; Muralidharan, D.; Perumal, P.T. Diastereoselective synthesis of cis-fused pyrano and furanobenzopyrans catalyzed by indium trichloride or triphenyl phosphonium perchlorate. Tetrahedron 2002, 58, 10301.
    • (2002) Tetrahedron , vol.58 , pp. 10301
    • Anniyappan, M.1    Muralidharan, D.2    Perumal, P.T.3
  • 45
    • 0026714006 scopus 로고
    • Recent developments in the synthesis of C-glycosides
    • Postema, M.H.D. Recent developments in the synthesis of C-glycosides. Tetrahedron 1992, 48, 8545.
    • (1992) Tetrahedron , vol.48 , pp. 8545
    • Postema, M.H.D.1
  • 47
    • 34547892223 scopus 로고    scopus 로고
    • Enantiospecific synthesis of the heparanase inhibitor (+)-trachyspic acid and stereoisomers from a common precursor
    • Zammit, S.C.; Ferro, V.; Hammond, E.; Rizzacasa, M. A. Enantiospecific synthesis of the heparanase inhibitor (+)-trachyspic acid and stereoisomers from a common precursor. Org. Biomol. Chem. 2007, 5, 2826.
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 2826
    • Zammit, S.C.1    Ferro, V.2    Hammond, E.3    Rizzacasa, M.A.4
  • 48
    • 1842635726 scopus 로고    scopus 로고
    • Montmorillonite clay catalyzed alkylation of pyrroles and indoles with cyclic hemi-acetals
    • Yadav, J.S.; Reddy, B.V.S.; Satheesh, G. Montmorillonite clay catalyzed alkylation of pyrroles and indoles with cyclic hemi-acetals. Tetrahedron Lett. 2004, 45, 3673.
    • (2004) Tetrahedron Lett , vol.45 , pp. 3673
    • Yadav, J.S.1    Reddy, B.V.S.2    Satheesh, G.3
  • 49
    • 35348994878 scopus 로고    scopus 로고
    • The first examples of cyclizations of a glycal with enamines leading to oxa-aza bicyclononene scaffolds
    • Yadav, J. S.; Reddy, B. V. S.; Srinivas, M.;. Divyavani, Ch.; Kunwar, A. C.; Madavi, Ch. The first examples of cyclizations of a glycal with enamines leading to oxa-aza bicyclononene scaffolds. Tetrahedron Lett. 2007, 48, 8301.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 8301
    • Yadav, J.S.1    Reddy, B.V.S.2    Srinivas, M.3    Divyavani, Ch.4    Kunwar, A.C.5    Madavi, C.6
  • 51
    • 42149104568 scopus 로고    scopus 로고
    • Three-Component Reaction of Aldose Sugars, Aryl Amines, and 1,3-Diones: A Novel Synthesis of Annulated Pyrroles
    • Yadav, J.S.; Reddy, B.V.S.; Srinivas, M. Three-Component Reaction of Aldose Sugars, Aryl Amines, and 1,3-Diones: A Novel Synthesis of Annulated Pyrroles. J. Org. Chem. 2008, 73, 3252.
    • (2008) J. Org. Chem. , vol.73 , pp. 3252
    • Yadav, J.S.1    Reddy, B.V.S.2    Srinivas, M.3
  • 52
    • 0032482080 scopus 로고    scopus 로고
    • Modern Variants of the Mannich Reaction
    • and references cited therein
    • Risch, N.; Arend, M.; Westermann, B. Modern Variants of the Mannich Reaction. Angew. Chem. Int. Ed. Engl. 1998, 37, 1044 and references cited therein.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 1044
    • Risch, N.1    Arend, M.2    Westermann, B.3
  • 54
    • 0003417469 scopus 로고
    • Trost, B.M., Fleming, I. Eds.; Pergamon: Oxford and references cited therein
    • Volkmann, R.A. In: Comprehensive Organic Synthesis; Trost, B.M., Fleming, I. Eds.; Pergamon: Oxford, 1991; Vol. 1, p. 355 and references cited therein.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 355
    • Volkmann, R.A.1
  • 55
    • 0034640471 scopus 로고    scopus 로고
    • Three component synthesis of β-Amino carbonyl compounds using indium trichloride-catalyzed onepot mannich-type reaction in water
    • Loh, T.-.P; Sarah, B.K.W.; Tan, K.-L.; Wei, L.-L. Three component synthesis of β-Amino carbonyl compounds using indium trichloride-catalyzed onepot mannich-type reaction in water. Tetrahedron 2000, 56, 3227.
    • (2000) Tetrahedron , vol.56 , pp. 3227
    • Loh, T.-P.1    Sarah, B.K.W.2    Tan, K.-L.3    Wei, L.-L.4
  • 56
    • 0037430431 scopus 로고    scopus 로고
    • Asymmetric Mannich-type reactions catalyzed by indium(III) complexes in ionic liquids
    • Chen, S.-L.; Ji, S.-J.; Loh, T.-P. Asymmetric Mannich-type reactions catalyzed by indium(III) complexes in ionic liquids. Tetrahedron Lett. 2003, 44, 2405.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2405
    • Chen, S.-L.1    Ji, S.-J.2    Loh, T.-P.3
  • 57
    • 33947728862 scopus 로고    scopus 로고
    • Design and synthesis of a Water-Tolerant chiral indium complex: -application to one-pot three-component mannich-type reactions in water
    • Xiao, J.; Loh, T.-P. Design and synthesis of a Water-Tolerant chiral indium complex: -application to one-pot three-component mannich-type reactions in water. Synlett. 2007, 5, 815.
    • (2007) Synlett , vol.5 , pp. 815
    • Xiao, J.1    Loh, T.-P.2
  • 59
    • 0028355337 scopus 로고
    • Recent developments in the stereoselective synthesis of α-aminoacids
    • Duthaler, R.O. Recent developments in the stereoselective synthesis of α-aminoacids. Tetrahedron 1994, 50, 1539.
    • (1994) Tetrahedron , vol.50 , pp. 1539
    • Duthaler, R.O.1
  • 61
    • 0030821811 scopus 로고    scopus 로고
    • Amino Acid Derivatives by Multicomponent Reactions
    • Dyker, G. Amino Acid Derivatives by Multicomponent Reactions. Angew. Chem. Int. Ed. 1997, 36, 1700.
    • (1997) Angew. Chem. Int. Ed. , vol.36 , pp. 1700
    • Dyker, G.1
  • 62
    • 0035793657 scopus 로고    scopus 로고
    • Recent Developments in Catalytic Asymmetric Strecker-Type Reactions
    • Yet, L. Recent Developments in Catalytic Asymmetric Strecker-Type Reactions. Angew. Chem. Int. Ed. 2001, 40, 875.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 875
    • Yet, L.1
  • 63
    • 0034400108 scopus 로고    scopus 로고
    • Some recent applications of -amino nitrile chemistry
    • Enders, D.; Shilvock, J.P. Some recent applications of -amino nitrile chemistry. Chem. Soc. Rev. 2000, 29, 359.
    • (2000) Chem. Soc. Rev. , vol.29 , pp. 359
    • Enders, D.1    Shilvock, J.P.2
  • 65
    • 0032492926 scopus 로고    scopus 로고
    • Lithium perchlorate/ diethylether catalyzed aminocyanation of aldehydes
    • Heydari, A.; Fatemi, P.; Alizadeh, A.A. Lithium perchlorate/ diethylether catalyzed aminocyanation of aldehydes. Tetrahedron Lett. 1998, 39, 3049.
    • (1998) Tetrahedron Lett , vol.39 , pp. 3049
    • Heydari, A.1    Fatemi, P.2    Alizadeh, A.A.3
  • 66
    • 1842481465 scopus 로고    scopus 로고
    • Lithium Perchlorate Mediated Three-Component Preparation of α-Aminonitriles Under Solvent-Free Conditions
    • Azizi, N.; Saidi, M.R. Lithium Perchlorate Mediated Three-Component Preparation of α-Aminonitriles Under Solvent-Free Conditions. Synth. Commun. 2004, 34, 1207.
    • (2004) Synth. Commun. , vol.34 , pp. 1207
    • Azizi, N.1    Saidi, M.R.2
  • 67
    • 11144329128 scopus 로고    scopus 로고
    • Lithium perchlorate suspend in methylene chloride, a mild, efficient and reusable catalyst for the synthesis of ferrocene aminonitrile derivatives
    • Yousefi, R.; Azizi, N.; Saidi, M.R. Lithium perchlorate suspend in methylene chloride, a mild, efficient and reusable catalyst for the synthesis of ferrocene aminonitrile derivatives. J. Organomet. Chem. 2005, 690, 76.
    • (2005) J. Organomet. Chem. , vol.690 , pp. 76
    • Yousefi, R.1    Azizi, N.2    Saidi, M.R.3
  • 68
    • 4444356723 scopus 로고    scopus 로고
    • Bismuth trichloride catalyzed synthesis of α-aminonitriles
    • De, S.K.; Gibbs, R.A. Bismuth trichloride catalyzed synthesis of α-aminonitriles. Tetrahedron Lett. 2004, 45, 7407.
    • (2004) Tetrahedron Lett , vol.45 , pp. 7407
    • De, S.K.1    Gibbs, R.A.2
  • 69
    • 33947711966 scopus 로고    scopus 로고
    • Sulfamic Acid Catalyzed Direct Condensation of Aldehydes, Amines, and TMSCN to α-Aminonitriles at Ambient Temperature
    • Li, Z.J.; Sun, Y.J.; Ren, X.H.; Wei, P.; Shi, Y.H.; Ouyang, P.K. Sulfamic Acid Catalyzed Direct Condensation of Aldehydes, Amines, and TMSCN to α-Aminonitriles at Ambient Temperature. Synlett 2007, 803.
    • (2007) Synlett , pp. 803
    • Li, Z.J.1    Sun, Y.J.2    Ren, X.H.3    Wei, P.4    Shi, Y.H.5    Ouyang, P.K.6
  • 70
    • 28944441150 scopus 로고    scopus 로고
    • 3: an efficient homogeneous and solid-supported promoter for aza and thia-Michael reactions and for Strecker reactions
    • 3: an efficient homogeneous and solid-supported promoter for aza and thia-Michael reactions and for Strecker reactions. Tetrahedron 2006, 62, 440.
    • (2006) Tetrahedron , vol.62 , pp. 440
    • Fetterly, B.M.1    Jana, N.K.2    Verkade, J.G.3
  • 71
    • 34247860574 scopus 로고    scopus 로고
    • Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the threecomponent synthesis of α-amino nitriles
    • Heydari, A.; Khaksar, S.; Pourayoubi, M.; Mahjoub, A.R. Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the three-component synthesis of α-amino nitriles. Tetrahedron Lett. 2007, 48, 4059.
    • (2007) Tetrahedron Lett , vol.48 , pp. 4059
    • Heydari, A.1    Khaksar, S.2    Pourayoubi, M.3    Mahjoub, A.R.4
  • 72
    • 33745590830 scopus 로고    scopus 로고
    • 3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of α-aminonitriles
    • 3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of α-aminonitriles. Tetrahedron Lett. 2006, 47, 5759.
    • (2006) Tetrahedron Lett , vol.47 , pp. 5759
    • Paraskar, A.S.1    Sudalai, A.2
  • 73
    • 27644482318 scopus 로고    scopus 로고
    • Catalyst-free multicomponent Strecker reaction in acetonitrile
    • Martinez, R.; Ramon, D.J.; Yus, M. Catalyst-free multicomponent Strecker reaction in acetonitrile. Tetrahedron Lett. 2005, 46, 8471.
    • (2005) Tetrahedron Lett , vol.46 , pp. 8471
    • Martinez, R.1    Ramon, D.J.2    Yus, M.3
  • 74
    • 0037170892 scopus 로고    scopus 로고
    • Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide
    • Ranu, B.C.; Dey, S.S.; Hajra, A. Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide. Tetrahedron 2002, 58, 2529.
    • (2002) Tetrahedron , vol.58 , pp. 2529
    • Ranu, B.C.1    Dey, S.S.2    Hajra, A.3
  • 75
    • 47049127635 scopus 로고    scopus 로고
    • Indium(III) iodide-mediated Strecker reaction in water: an efficient and environmentally friendly approach for the synthesis of α-aminonitrile via a three-component condensation
    • Shen, S.-L.; Ji, S.-H.; Loh, T.-P. Indium(III) iodide-mediated Strecker reaction in water: an efficient and environmentally friendly approach for the synthesis of α-aminonitrile via a three-component condensation. Tetrahedron 2008, 64, 8159.
    • (2008) Tetrahedron , vol.64 , pp. 8159
    • Shen, S.-L.1    Ji, S.-H.2    Loh, T.-P.3
  • 76
    • 68749085966 scopus 로고    scopus 로고
    • Design and synthesis of ∈-aminonitrile-functionalized retinoids
    • Bhaskar, C.D.; Anguiano, J.; Mahalingam, S.M. Design and synthesis of ∈-aminonitrile-functionalized retinoids. Tetrahedron Lett. 2009, 50, 5670.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 5670
    • Bhaskar, C.D.1    Anguiano, J.2    Mahalingam, S.M.3
  • 77
    • 0034519777 scopus 로고    scopus 로고
    • Biologically active dihydropyrimidones of the Biginelli-type - a literature survey
    • Kappe, C.O. Biologically active dihydropyrimidones of the Biginelli-type - a literature survey. Eur. J. Med. Chem. 2000, 35, 1043-1052.
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1043-1052
    • Kappe, C.O.1
  • 78
    • 0034708729 scopus 로고    scopus 로고
    • X-Ray Structure, Con-formational Analysis, Enantioseparation, and Determination of Absolute Configuration of the Mitotic Kinesin Eg5 Inhibitor Monastrol
    • Kappe, C.O.; Shishkin, O.V.; Uray, G.; Verdino, P. X-Ray Structure, Con-formational Analysis, Enantioseparation, and Determination of Absolute Configuration of the Mitotic Kinesin Eg5 Inhibitor Monastrol. Tetrahedron 2000, 56, 1859.
    • (2000) Tetrahedron , vol.56 , pp. 1859
    • Kappe, C.O.1    Shishkin, O.V.2    Uray, G.3    Verdino, P.4
  • 80
    • 0000176059 scopus 로고
    • Synthesis of 3,4-dihydropyrimidine-2(1H)-ones. Gazz
    • Biginelli, P. Synthesis of 3,4-dihydropyrimidine-2(1H)-ones. Gazz. Chim. Ital. 1893, 23, 360.
    • (1893) Chim. Ital. , vol.23 , pp. 360
    • Biginelli, P.1
  • 81
    • 0037054171 scopus 로고    scopus 로고
    • Clovis Peppe Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction
    • Nan-Yan, F.; Yao -Feng, Y.; Zhong, C.; Shan-Wei, W.; Ji-Tao, W. Clovis Peppe Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction. Tetrahedron 2002, 4801.
    • (2002) Tetrahedron , pp. 4801
    • Nan -Yan, F.1    Yao-Feng, Y.2    Zhong, C.3    Shan-Wei, W.4    Ji-Tao, W.5
  • 83
    • 0000917692 scopus 로고
    • Nitriles in Heterocyclic Synthesis: Novel Synthesis of Benzo[c]coumarin and of Benzo[c]pyrano[3,2-c]quinoline Derivatives
    • Hafez, E.A.; Elnagdi, M.H.; Elagamey, A.G.A.; El-Taweel, F.M.A.A. Nitriles in Heterocyclic Synthesis: Novel Synthesis of Benzo[c]coumarin and of Benzo[c]pyrano[3,2-c]quinoline Derivatives. Heterocycles 1987, 26, 903.
    • (1987) Heterocycles , vol.26 , pp. 903
    • Hafez, E.A.1    Elnagdi, M.H.2    Elagamey, A.G.A.3    El-Taweel, F.M.A.A.4
  • 84
    • 0031555345 scopus 로고    scopus 로고
    • DNA strand breaking activity and mutagenicity of a Maillard reaction product, 2,3-dihydro-3,5-dihydroxy-6-methyl-4h-pyran-4-one
    • Hiramoto, K.; Nasuhara, A.; Michikoshi, K.; Kato, T.; Kikugawa, K. DNA strand breaking activity and mutagenicity of a Maillard reaction product, 2,3-dihydro-3,5-dihydroxy-6-methyl-4h-pyran-4-one. Mutat. Res. 1997, 395, 47.
    • (1997) Mutat. Res. , vol.395 , pp. 47
    • Hiramoto, K.1    Nasuhara, A.2    Michikoshi, K.3    Kato, T.4    Kikugawa, K.5
  • 85
    • 84859299701 scopus 로고
    • Synthesis of (2R)(+)-2,3-dihydro-2,6-dimethyl-4H-pyran-4-one, a homologue of pheromones of a species in the hepialidae family
    • Bianchi, G.; Tava, A. Synthesis of (2R)(+)-2,3-dihydro-2,6-dimethyl-4H-pyran-4-one, a homologue of pheromones of a species in the hepialidae family. Agric. Biol. Chem. 1987, 51, 2001.
    • (1987) Agric. Biol. Chem. , vol.51 , pp. 2001
    • Bianchi, G.1    Tava, A.2
  • 86
    • 34548038657 scopus 로고    scopus 로고
    • An eco-friendly synthesis of 2-aminochromenes and indolyl chromenes catalyzed by InCl3 in aqueous media
    • Shanthi, G.; Perumal, P.T. An eco-friendly synthesis of 2-aminochromenes and indolyl chromenes catalyzed by InCl3 in aqueous media. Tetrahedron Lett. 2007, 48, 6785.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 6785
    • Shanthi, G.1    Perumal, P.T.2
  • 87
    • 4243893500 scopus 로고
    • Selective reactions using allylic metals
    • Yamamoto, Y.; Asao, N. Selective reactions using allylic metals. Chem. Rev. 1993, 93, 2207.
    • (1993) Chem. Rev. , vol.93 , pp. 2207
    • Yamamoto, Y.1    Asao, N.2
  • 88
    • 0000862669 scopus 로고    scopus 로고
    • Catalytic Enantioselective Addition to Imines
    • Kobayashi, S.; Ishitani, H. Catalytic Enantioselective Addition to Imines. Chem. Rev. 1999, 99, 1069.
    • (1999) Chem. Rev. , vol.99 , pp. 1069
    • Kobayashi, S.1    Ishitani, H.2
  • 89
    • 0037099190 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Propargylamines by Copper-Catalyzed Addition of Alkynes to Enamines
    • Koradin, C.; Polborn, K.; Knochel, P. Enantioselective Synthesis of Propargylamines by Copper-Catalyzed Addition of Alkynes to Enamines. Angew. Chem. Int. Ed. 2002, 41, 2535.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2535
    • Koradin, C.1    Polborn, K.2    Knochel, P.3
  • 90
    • 0037157090 scopus 로고    scopus 로고
    • Enantioselective Direct-Addition of Terminal Alkynes to Imines Catalyzed by Copper(I)pybox Complex in Water and in Toluene
    • Wei, C.; Li, C.-J. Enantioselective Direct-Addition of Terminal Alkynes to Imines Catalyzed by Copper(I)pybox Complex in Water and in Toluene. J. Am. Chem. Soc. 2002, 124, 5638.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5638
    • Wei, C.1    Li, C.-J.2
  • 91
    • 0346243940 scopus 로고    scopus 로고
    • Enantioselective, Copper(I)-Catalyzed Three-Component Reaction for the Preparation of Propargylamines
    • Gommermann, N.; Koradin, C.; Polborn, K.; Knochel, P. Enantioselective, Copper(I)-Catalyzed Three-Component Reaction for the Preparation of Propargylamines. Angew. Chem. Int. Ed. 2003, 42, 5763.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5763
    • Gommermann, N.1    Koradin, C.2    Polborn, K.3    Knochel, P.4
  • 92
    • 22244487956 scopus 로고    scopus 로고
    • Chiral Diamine-Copper(I) Complexes as Asymmetric Catalysts in the Enantioselective Addition of Phenylacetylene to Imines
    • Orlandi, S.; Colombo, F.; Benaglia, M. Chiral Diamine-Copper(I) Complexes as Asymmetric Catalysts in the Enantioselective Addition of Phenylacetylene to Imines. Synthesis 2005, 1689.
    • (2005) Synthesis , pp. 1689
    • Orlandi, S.1    Colombo, F.2    Benaglia, M.3
  • 93
    • 1642487346 scopus 로고    scopus 로고
    • Microwave-Promoted Three-Component Coupling of Aldehyde, Alkyne, and Amine via C-H Activation Catalyzed by Copper in Water
    • Shi, L.; Tu, Y.-Q.; Wang, M.; Zhang, F.-M.; Fa, C.-A. Microwave-Promoted Three-Component Coupling of Aldehyde, Alkyne, and Amine via C-H Activation Catalyzed by Copper in Water. Org. Lett. 2004, 6, 1001.
    • (2004) Org. Lett. , vol.6 , pp. 1001
    • Shi, L.1    Tu, Y.-Q.2    Wang, M.3    Zhang, F.-M.4    Fa, C.-A.5
  • 94
    • 24344476717 scopus 로고    scopus 로고
    • Ultrasound-assisted rapid and efficient synthesis of propargylamines
    • Sreedhar, B.; Reddy, P.S.; Prakash, B.V.; Ravindra, A. Ultrasound-assisted rapid and efficient synthesis of propargylamines. Tetrahedron Lett. 2005, 46, 7019.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7019
    • Sreedhar, B.1    Reddy, P.S.2    Prakash, B.V.3    Ravindra, A.4
  • 95
    • 4444286248 scopus 로고    scopus 로고
    • Hydroxyapatite supported copper catalyst for effective three-component coupling
    • Choudary, B. M.; Sridhar, C.; Kantam, M. L.; Sreedhar, B. Hydroxyapatite supported copper catalyst for effective three-component coupling. Tetrahedron Lett. 2004, 45, 7319.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7319
    • Choudary, B.M.1    Sridhar, C.2    Kantam, M.L.3    Sreedhar, B.4
  • 96
    • 34248524887 scopus 로고    scopus 로고
    • A highly efficient three-component coupling of aldehyde, terminal alkyne, and amine via C-H activation catalyzed by reusable immobilized copper in organic-inorganic hybrid materials under solvent-free reaction conditions
    • Li, P.; Wang, L. A highly efficient three-component coupling of aldehyde, terminal alkyne, and amine via C-H activation catalyzed by reusable immobilized copper in organic-inorganic hybrid materials under solvent-free reaction conditions. Tetrahedron 2007, 63, 5455.
    • (2007) Tetrahedron , vol.63 , pp. 5455
    • Li, P.1    Wang, L.2
  • 97
    • 65549097384 scopus 로고    scopus 로고
    • InBr3-catalyzed three-component reaction: a facile synthesis of propargyl amines
    • Yadav, J.S.; Subba Reddy, B.V.; Hara Gopal, A.V.; Patil, K.S. InBr3-catalyzed three-component reaction: a facile synthesis of propargyl amines. Tetrahedron Lett. 2009, 50, 3493.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 3493
    • Yadav, J.S.1    Subba Reddy, B.V.2    Hara Gopal, A.V.3    Patil, K.S.4
  • 98
    • 85197357792 scopus 로고
    • U.S. Patent 3,338,915
    • Brown, M. U.S. Patent 3,338,915, 1967.
    • (1967)
    • Brown, M.1
  • 99
    • 0041519440 scopus 로고    scopus 로고
    • Barry Sharpless Why Is Tetrazole Formation by Addition of Azide to Organic Nitriles Catalyzed by Zinc(II)Salts?
    • Fahmi Himo, Zachary P. Demko, Louis Noodleman, K. Barry Sharpless Why Is Tetrazole Formation by Addition of Azide to Organic Nitriles Catalyzed by Zinc(II)Salts? J. Am. Chem. Soc. 2003, 125, 9983.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 9983
    • Fahmi, H.1    Demko, Z.P.2    Louis Noodleman, K.3
  • 101
    • 0025995750 scopus 로고
    • Isosterism and bioisosterism in drug design
    • Burger, A. Isosterism and bioisosterism in drug design. Prog. Drug Res. 1991, 37, 287.
    • (1991) Prog. Drug Res. , vol.37 , pp. 287
    • Burger, A.1
  • 102
    • 0025917285 scopus 로고
    • Studies concerning the acidity and the distribution behaviour of 1-phenyl-5-mercaptotetrazole
    • Ruelke, H.; Friedel, A.; Martin, E.; Kottke, K.; Graefe, I.; Kuhmstedt, H. Studies concerning the acidity and the distribution behaviour of 1-phenyl-5-mercaptotetrazole. Pharmazie 1991, 46, 456.
    • (1991) Pharmazie , vol.46 , pp. 456
    • Ruelke, H.1    Friedel, A.2    Martin, E.3    Kottke, K.4    Graefe, I.5    Kuhmstedt, H.6
  • 104
    • 0011428887 scopus 로고
    • Synthesis of 1-Substituted tetrazoles
    • Fallon, F.G.; Herbst, R.M. Synthesis of 1-Substituted tetrazoles. J. Org. Chem. 1957, 22, 933.
    • (1957) J. Org. Chem. , vol.22 , pp. 933
    • Fallon, F.G.1    Herbst, R.M.2
  • 105
    • 85197343482 scopus 로고
    • U.S. Patent 3,767,667
    • Kamiya, T.; Saito, Y. U.S. Patent 3,767,667, 1973.
    • (1973)
    • Kamiya, T.1    Saito, Y.2
  • 106
    • 0028967106 scopus 로고
    • Nicholas marcopulos application of 5-Lithiotetrazoles in organic synthesis
    • Satoh, Y. Nicholas marcopulos application of 5-Lithiotetrazoles in organic synthesis. Tetrahedron Lett. 1995, 36, 1759.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1759
    • Satoh, Y.1
  • 107
    • 64249107551 scopus 로고    scopus 로고
    • Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4-tetrazoles under solvent-free conditions
    • Kundu, D.; Majee, A.; Hajra, A. Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4-tetrazoles under solvent-free conditions. Tetrahedron Lett. 2009, 50, 2668.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2668
    • Kundu, D.1    Majee, A.2    Hajra, A.3
  • 108
    • 0037037851 scopus 로고    scopus 로고
    • Remarkable enhancement of Lewis acidity of chlorosilane by the combined use of indium(III) chloride
    • Onishi, Y.; Ito. T.; Yasuda, M.; Baba, A. Remarkable enhancement of Lewis acidity of chlorosilane by the combined use of indium(III) chloride. Tetrahedron 2002, 58, 8227.
    • (2002) Tetrahedron , vol.58 , pp. 8227
    • Onishi, Y.1    Ito, T.2    Yasuda, M.3    Baba, A.4
  • 109
    • 36849062647 scopus 로고    scopus 로고
    • Coupling reaction of alkyl chlorides with silyl enolates catalyzed by indium trihalide
    • Nishimoto, Y.; Yasuda, M.; Baba, A. Coupling reaction of alkyl chlorides with silyl enolates catalyzed by indium trihalide. Org. Lett. 2007, 9, 4931.
    • (2007) Org. Lett. , vol.9 , pp. 4931
    • Nishimoto, Y.1    Yasuda, M.2    Baba, A.3
  • 110
    • 23944471213 scopus 로고    scopus 로고
    • Indium trichloride catalyzed synthesis of 2-Aryl-3-aminobenzofuran-derivatives by a three-component reaction of phenols, arylglyoxal-monohydrates and paratoluenesulfonamide
    • Chen, L.-X.; Liu, L.; Yang, D.P.; Wang, D.; Chen, Y.-C. Indium trichloride catalyzed synthesis of 2-Aryl-3-aminobenzofuran-derivatives by a three-component reaction of phenols, arylglyoxal-monohydrates and paratoluenesulfonamide. Synlett 2005, 2047.
    • (2005) Synlett , pp. 2047
    • Chen, L.-X.1    Liu, L.2    Yang, D.P.3    Wang, D.4    Chen, Y.-C.5


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