메뉴 건너뛰기




Volumn 15, Issue 14, 2011, Pages 2438-2468

Molecular iodine: Recent application in heterocyclic synthesis

Author keywords

Catalyst; Heterocyclic compounds; Molecular iodine; Synthesis

Indexed keywords

CATALYSTS; IODINE; ORGANIC COMPOUNDS;

EID: 79959939849     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211796150570     Document Type: Review
Times cited : (60)

References (133)
  • 1
    • 85196230108 scopus 로고    scopus 로고
    • Springer: Berlin
    • Org. Synth., Coll. Vol. II; Springer: Berlin, 966, 428.
    • Org. Synth., Coll. , vol.2
  • 2
    • 33748699338 scopus 로고    scopus 로고
    • Synthetic use of molecular iodine for organic synthesis
    • Togo, H.; Iida, S. Synthetic use of molecular iodine for organic synthesis. Synlett, 2006, 2159-2175.
    • (2006) Synlett , pp. 2159-2175
    • Togo, H.1    Iida, S.2
  • 3
    • 9644287844 scopus 로고    scopus 로고
    • Molecular iodine
    • Wang, S.-Y. Molecular iodine. Synlett, 2004, 2642-2643.
    • (2004) Synlett , pp. 2642-2643
    • Wang, S.-Y.1
  • 5
    • 56849088735 scopus 로고    scopus 로고
    • Molecular iodine in protection and deprotection chemistry
    • Das, S.; Borah, R.; Rekha Devi, R.; Thakur, A.J. Molecular iodine in protection and deprotection chemistry. Synlett, 2008, 2741-2762.
    • (2008) Synlett , pp. 2741-2762
    • Das, S.1    Borah, R.2    Rekha Devi, R.3    Thakur, A.J.4
  • 8
    • 0032578675 scopus 로고    scopus 로고
    • Iodine-catalyzed aziridination of alkenes using Chloramine-T as a nitrogen source
    • Ando, T.; Kano, D.; Minakata, S.; Ryu, I.; Komatsu, M. Iodine-catalyzed aziridination of alkenes using Chloramine-T as a nitrogen source, Tetrahedron, 1998, 54, 3485-13494.
    • (1998) Tetrahedron , vol.54 , pp. 3485-13494
    • Ando, T.1    Kano, D.2    Minakata, S.3    Ryu, I.4    Komatsu, M.5
  • 9
    • 1042287074 scopus 로고    scopus 로고
    • Synthesis of??-lactams and??- aminoesters via high intensity ultrasound-promoted Reformatsky
    • Ross, N.A.; MacGregor, R.R.; Bartsch, R.A. Synthesis of??-lactams and??- aminoesters via high intensity ultrasound-promoted Reformatsky. Tetrahedron, 2004, 60, 2035-2041.
    • (2004) Tetrahedron , vol.60 , pp. 2035-2041
    • Ross, N.A.1    Macgregor, R.R.2    Bartsch, R.A.3
  • 11
    • 0037121848 scopus 로고    scopus 로고
    • Cleavage of epoxides into halohydrins with elemental iodine and bromine in the presence of 2,6-bis[2-(oaminophenoxy) methyl]-4-bromo-1- methoxybenzene (BABMB) as catalyst
    • Niknam, K.; Nasehi, T. Cleavage of epoxides into halohydrins with elemental iodine and bromine in the presence of 2,6-bis[2-(oaminophenoxy) methyl]-4-bromo-1- methoxybenzene (BABMB) as catalyst. Tetrahedron, 2002, 58, 10259-10261.
    • (2002) Tetrahedron , vol.58 , pp. 10259-10261
    • Niknam, K.1    Nasehi, T.2
  • 12
    • 0010295691 scopus 로고
    • Ethylenimine ketones. XI. steric controls in the formation of isomeric ethylenimine ketones
    • Cromwell, N.H.; Cahoyw, R.P.; Franklin, W.E.; Mercer, G.D. Ethylenimine ketones. XI. steric controls in the formation of isomeric ethylenimine ketones. J. Org. Chem., 1957, 79, 922-926.
    • (1957) J. Org. Chem. , vol.79 , pp. 922-926
    • Cromwell, N.H.1    Cahoyw, R.P.2    Franklin, W.E.3    Mercer, G.D.4
  • 13
    • 0028555488 scopus 로고
    • A synthetic study on the preparation of triarylmethanes
    • Muthyala, R.; Katritzky, K.A.R.; Lan, X. A synthetic study on the preparation of triarylmethanes. Dyes Pigm., 1994, 25, 303-324.
    • (1994) Dyes Pigm. , vol.25 , pp. 303-324
    • Muthyala, R.1    Katritzky, K.A.R.2    Lan, X.3
  • 14
    • 0035766144 scopus 로고    scopus 로고
    • Dication species stabilized by heteroazulenes: Synthesis and properties of 1,3- and 1,4-bis[bis(2-oxo-2H-cyclohepta[b]furan-3- yl)methyliumyl]-, bis[bis(1,2-dihydro-N-methyl-2-oxocyclohepta[b]pyrrol-3- yl)methyliumyl]benzene, and their related dications
    • Naya, S.J.; Nitta, M. Dication species stabilized by heteroazulenes: synthesis and properties of 1,3- and 1,4-bis[bis(2-oxo-2H-cyclohepta[b]furan-3- yl)methyliumyl]-, bis[bis(1,2-dihydro-N-methyl-2-oxocyclohepta[b]pyrrol-3- yl)methyliumyl]benzene, and their related dications. J. Chem. Soc. Perkin Trans. 2, 2001, 2, 275-281.
    • (2001) J. Chem. Soc. Perkin Trans. 2 , vol.2 , pp. 275-281
    • Naya, S.J.1    Nitta, M.2
  • 15
    • 0035925731 scopus 로고    scopus 로고
    • Synthesis of novel cage molecules bicapped with tris(2-thienyl)methanes
    • Kurata, H.; Nakamini, H.; Matsumoto, K.; Kawase, T.; Oda, M. Synthesis of novel cage molecules bicapped with tris(2-thienyl)methanes. Chem. Commun., 2001, 529-530.
    • (2001) Chem. Commun. , pp. 529-530
    • Kurata, H.1    Nakamini, H.2    Matsumoto, K.3    Kawase, T.4    Oda, M.5
  • 16
    • 0035817289 scopus 로고    scopus 로고
    • Reactions between pyrrole and orthoesters: Preparation of tri- (pyrrol-2-yl)alkanes
    • Reese, C.B.; Yan, H. Reactions between pyrrole and orthoesters: preparation of tri- (pyrrol-2-yl)alkanes. Tetrahedron Lett., 2001, 42, 5545-5547.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 5545-5547
    • Reese, C.B.1    Yan, H.2
  • 17
    • 0037175486 scopus 로고    scopus 로고
    • Novel intramolecular photocyclization of tris(2-benzo[b]thienyl)methyl alcohol
    • Tanifugi, N.; Huang, H.; Shinagawa, Y.; Kobayashi, K. Novel intramolecular photocyclization of tris(2-benzo[b]thienyl)methyl alcohol. Tetrahedron Lett., 2002, 43, 8669-8672.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 8669-8672
    • Tanifugi, N.1    Huang, H.2    Shinagawa, Y.3    Kobayashi, K.4
  • 18
    • 42549149040 scopus 로고    scopus 로고
    • Facile Synthesis of symmetrical triindolylmethanes catalyzed by iodine under solvent-free condition
    • Xiao-Fei, Z.; Shun-Jun, J.; Xiao-Ming, S. Facile Synthesis of symmetrical triindolylmethanes catalyzed by iodine under solvent-free condition. Chin. J. Chem., 2008, 26, 413.
    • (2008) Chin. J. Chem. , vol.26 , pp. 413
    • Xiao-Fei, Z.1    Shun-Jun, J.2    Xiao-Ming, S.3
  • 19
    • 0037463441 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions
    • Bandgar, B.P.; Shaikh, K.A. Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions. Tetrahedron Lett., 2003, 44, 1959-1961.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 1959-1961
    • Bandgar, B.P.1    Shaikh, K.A.2
  • 20
    • 1042298780 scopus 로고    scopus 로고
    • Facile synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions
    • Wang, S.; Zhang, Y.; Loh, T. Facile synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions. Tetrahedron, 2004, 60, 2051-2055.
    • (2004) Tetrahedron , vol.60 , pp. 2051-2055
    • Wang, S.1    Zhang, Y.2    Loh, T.3
  • 21
    • 13744259489 scopus 로고    scopus 로고
    • Preparation of bisindolylalkanes from N-tert-butanesulfinyl aldimines
    • Ke, B.; Qin, Y.; He, Q.; Huang, Z.; Wang, F. Preparation of bisindolylalkanes from N-tert-butanesulfinyl aldimines. Tetrahedron Lett., 2005, 46, 1751-1753.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 1751-1753
    • Ke, B.1    Qin, Y.2    He, Q.3    Huang, Z.4    Wang, F.5
  • 22
    • 19944423788 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed imine activation for three-component nucleophilic addition reactions
    • Lee, B.S.; Mahajan, S.; Janda, K.D. Molecular iodine-catalyzed imine activation for three-component nucleophilic addition reactions. Synlett, 2005, 1325-1327.
    • (2005) Synlett , pp. 1325-1327
    • Lee, B.S.1    Mahajan, S.2    Janda, K.D.3
  • 23
    • 38049180954 scopus 로고    scopus 로고
    • Facile formation of bis(3- indolyl)methylarenes by iodine-catalyzed reaction of indole with α, α'- bis(arylmethylene)ketones and β- substituted arylmethyleneketones in dry ethanol
    • Mallik, A.K.; Pal, R.; Mandal, T.K. Facile formation of bis(3- indolyl)methylarenes by iodine-catalyzed reaction of indole with α, α'- bis(arylmethylene)ketones and β- substituted arylmethyleneketones in dry ethanol. Indian J. Chem., 2007, 46B, 2056-2059.
    • (2007) Indian J. Chem. , vol.46 B , pp. 2056-2059
    • Mallik, A.K.1    Pal, R.2    Mandal, T.K.3
  • 24
    • 0346749663 scopus 로고    scopus 로고
    • The michael addition of indole to α, β-unsaturated ketones catalyzed by iodine at room temperature
    • Wang, S.; Ji, S.; Loh, T. The michael addition of indole to α, β-unsaturated ketones catalyzed by iodine at room temperature. Synlett, 2003, 2377-2379.
    • (2003) Synlett , pp. 2377-2379
    • Wang, S.1    Ji, S.2    Loh, T.3
  • 25
    • 17744376784 scopus 로고    scopus 로고
    • Iodine-catalyzed highly efficient Michael reaction of indoles under solvent-free condition
    • Banik, B.K.; Fernandez, M.; Alvarez, C. Iodine-catalyzed highly efficient Michael reaction of indoles under solvent-free condition. Tetrahedron Lett., 2005, 46, 2479-2482.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2479-2482
    • Banik, B.K.1    Fernandez, M.2    Alvarez, C.3
  • 26
    • 27644549976 scopus 로고    scopus 로고
    • I2- catalyzed Michael addition of indole and pyrrole to nitroolefins
    • Lin, C.; Hsu, J.; Sastry, M.N.V.; Fang, H.; Tu, Z.; Liu, J.; Ching-Fa, Y. I2- catalyzed Michael addition of indole and pyrrole to nitroolefins. Tetrahedron, 2005, 61, 11751-11757.
    • (2005) Tetrahedron , vol.61 , pp. 11751-11757
    • Lin, C.1    Hsu, J.2    Sastry, M.N.V.3    Fang, H.4    Tu, Z.5    Liu, J.6    Ching-Fa, Y.7
  • 27
    • 29144499032 scopus 로고    scopus 로고
    • CAN and iodinecatalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde
    • Ko, S.; Lin, C.; Tu, Z.; Wang, Y.; Wang, C.; Yao, C. CAN and iodinecatalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde. Tetrahedron Lett., 2006, 47, 487-492.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 487-492
    • Ko, S.1    Lin, C.2    Tu, Z.3    Wang, Y.4    Wang, C.5    Yao, C.6
  • 28
    • 0347991827 scopus 로고    scopus 로고
    • Simple synthesis of substituted pyrroles
    • Banik, B.K.; Samajdar, S.; Banik, I. Simple synthesis of substituted pyrroles. J. Org. Chem., 2004, 69, 213-216.
    • (2004) J. Org. Chem. , vol.69 , pp. 213-216
    • Banik, B.K.1    Samajdar, S.2    Banik, I.3
  • 29
    • 14544308311 scopus 로고    scopus 로고
    • Concise syntheses of the cruciferous phytoalexins brassilexin, sinalexin, wasalexins, and analogues: Expanding the scope of the vilsmeier formylation
    • Pedras, M.S.C.; Tha, M. Concise syntheses of the cruciferous phytoalexins brassilexin, sinalexin, wasalexins, and analogues: expanding the scope of the vilsmeier formylation. J. Org. Chem., 2005, 70, 1828-1834.
    • (2005) J. Org. Chem. , vol.70 , pp. 1828-1834
    • Pedras, M.S.C.1    Tha, M.2
  • 31
    • 28544451672 scopus 로고    scopus 로고
    • An efficient and one-pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation of carbon-nitrogen bonds in water
    • Gogoi, P.; Konwar, D. An efficient and one-pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation of carbon-nitrogen bonds in water. Tetrahedron Lett., 2006, 47, 79-82.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 79-82
    • Gogoi, P.1    Konwar, D.2
  • 32
    • 51949118124 scopus 로고    scopus 로고
    • Direct synthesis of protected enantiopure 5-cyano-3,4-dihydroxypyrrolidin-2-ones from β-lactam aldehydes catalyzed by iodine
    • Alcaide, B.; Almendros, P.; Cabrero, G.; Ruiza, M.P. Direct synthesis of protected enantiopure 5-cyano-3,4-dihydroxypyrrolidin-2-ones from β-lactam aldehydes catalyzed by iodine. Synthesis, 2008, 2835-2839.
    • (2008) Synthesis , pp. 2835-2839
    • Alcaide, B.1    Almendros, P.2    Cabrero, G.3    Ruiza, M.P.4
  • 33
    • 38149090205 scopus 로고    scopus 로고
    • Efficient synthesis of 2,4,5-triaryl substituted imidazoles under solvent free conditions at room temperature
    • Parveen, A.; Ahmed, M.R.S.; Shaikh, K.A.; Deshmukh, S.P.; Pawar, R.P. Efficient synthesis of 2,4,5-triaryl substituted imidazoles under solvent free conditions at room temperature. Arkivoc, 2007, (xvi), 12-18.
    • (2007) Arkivoc , Issue.xvi , pp. 12-18
    • Parveen, A.1    Ahmed, M.R.S.2    Shaikh, K.A.3    Deshmukh, S.P.4    Pawar, R.P.5
  • 34
    • 77953372167 scopus 로고    scopus 로고
    • Molecular Iodine as an efficient catalyst for the synthesis of indazole
    • Gaikwadl, D.D.; Pawar, S.A.R.P. Molecular Iodine as an efficient catalyst for the synthesis of indazole. Int. J. ChemTech Res., 2009, 1, 442.
    • (2009) Int. J. ChemTech Res. , vol.1 , pp. 442
    • Gaikwadl, D.D.1    Pawar, S.A.R.P.2
  • 35
    • 85196232064 scopus 로고    scopus 로고
    • Using molecular iodine in direct oxidative condensation of aldoses with diamines: An improved synthesis of aldo-benzimidazoles and aldonaphthimidazoles for carbohydrate analysis
    • Maggio-Hall, L.A., Dorrestein, P.C.; Escalante-Semerena, J.C.; Begley, T.P. Using molecular iodine in direct oxidative condensation of aldoses with diamines: an improved synthesis of aldo-benzimidazoles and aldonaphthimidazoles for carbohydrate analysis. Org. Lett., 2003, 5, 2211.
    • Org. Lett. , vol.2003 , pp. 5
    • Maggio-Hall, L.A.1    Dorrestein, P.C.2    Escalante-Semerena, J.C.3    Begley, T.P.4
  • 36
    • 43449130083 scopus 로고    scopus 로고
    • Using molecular iodine in direct oxidative condensation of aldoses with diamines: An improved synthesis of aldo-benzimidazoles and aldonaphthimidazoles for carbohydrate analysis
    • Lin, C.; Lai, P.-T.; Liao, S.K.-S.; Hung, W.-T.; Yang, W.-B.; Fang, J.-M. Using molecular iodine in direct oxidative condensation of aldoses with diamines: an improved synthesis of aldo-benzimidazoles and aldonaphthimidazoles for carbohydrate analysis. J. Org. Chem., 2008, 73, 3848-3853.
    • (2008) J. Org. Chem. , vol.73 , pp. 3848-3853
    • Lin, C.1    Lai, P.-T.2    Liao, S.K.-S.3    Hung, W.-T.4    Yang, W.-B.5    Fang, J.-M.6
  • 37
    • 33744996505 scopus 로고    scopus 로고
    • One-pot synthesis of 1,2,4,5-tetraarylimidazoles using molecular iodine as an efficient catalyst
    • Kidwai, M.; Mothsra, P.A one-pot synthesis of 1,2,4,5-tetraarylimidazoles using molecular iodine as an efficient catalyst. Tetrahedron Lett., 2006, 47, 5029-5031.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 5029-5031
    • Kidwai, M.1    Mothsra, P.A.2
  • 39
    • 84990131664 scopus 로고    scopus 로고
    • Katritzky, Rees, A.R.; Scriven, C.W.; Eds. E.F.V., Elsevier Science: Oxford
    • Grimmett, M.R. Comprehensive Heterocyclic Chemistry II, Vol. 3; Katritzky, Rees, A.R.; Scriven, C.W.; Eds. E.F.V., Elsevier Science: Oxford, 1996, 77-220.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.3 , pp. 77-220
    • Grimmett, M.R.1
  • 40
    • 0025261068 scopus 로고
    • Thiamine coenzyme models: Imidazolinium ylides and the reactions of 2-(hydroxyalkyl)imidazolines
    • Jones, R.C.F.; Nichols, J.R. Thiamine coenzyme models: Imidazolinium ylides and the reactions of 2-(hydroxyalkyl)imidazolines. Tetrahedron Lett., 1990, 31, 1771-1774.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1771-1774
    • Jones, R.C.F.1    Nichols, J.R.2
  • 41
    • 0032514834 scopus 로고    scopus 로고
    • Stereoselective synthesis of quaternary benzylic carbons using C2 symmetric imidazolines and tetrahydrofuran as electrophile
    • Langlois, Y.; Dalko, P.I. Stereoselective synthesis of quaternary benzylic carbons using C2 symmetric imidazolines and tetrahydrofuran as electrophile. J. Org. Chem., 1998, 63, 8107-8117.
    • (1998) J. Org. Chem. , vol.63 , pp. 8107-8117
    • Langlois, Y.1    Dalko, P.I.2
  • 42
    • 33845684296 scopus 로고    scopus 로고
    • Direct oxidative conversion of aldehydes and alcohols to 2- imidazolines and 2-oxazolines using molecular iodine
    • Ishihara, M.; Togo, H. Direct oxidative conversion of aldehydes and alcohols to 2- imidazolines and 2-oxazolines using molecular iodine. Tetrahedron, 2007, 63, 1474-1480.
    • (2007) Tetrahedron , vol.63 , pp. 1474-1480
    • Ishihara, M.1    Togo, H.2
  • 43
    • 32344435655 scopus 로고    scopus 로고
    • An efficient preparation of 2-imidazolines and imidazoles from aldehydes with molecular iodine and (diacetoxyiodo)benzene
    • Ishihara, M.; Togo, H. An efficient preparation of 2-imidazolines and imidazoles from aldehydes with molecular iodine and (diacetoxyiodo)benzene. Synlett, 2006, 227-230.
    • (2006) Synlett , pp. 227-230
    • Ishihara, M.1    Togo, H.2
  • 44
    • 35748964126 scopus 로고    scopus 로고
    • Iodine-catalyzed coupling of 4- hydroxyproline with isatins: An expeditious synthesis of 3- pyrrolyl indolin-2-ones
    • Yadav, J.S.; Reddy, S.B.V.; Jain, R.; Reddy, S.U.V. Iodine-catalyzed coupling of 4- hydroxyproline with isatins: An expeditious synthesis of 3- pyrrolyl indolin-2-ones. J. Mol. Catal. A: Chem.; 2007, 278, 38-41.
    • (2007) J. Mol. Catal. A: Chem. , vol.278 , pp. 38-41
    • Yadav, J.S.1    Reddy, S.B.V.2    Jain, R.3    Reddy, S.U.V.4
  • 45
    • 33746292136 scopus 로고    scopus 로고
    • An efficient method to synthesize benzofurans and naphthofurans
    • Pan, C.; Yu, J.; Zhou, Y.; Wang, Z.; Zhou, M.-M. An efficient method to synthesize benzofurans and naphthofurans. Synlett, 2006, 1657-1662.
    • (2006) Synlett , pp. 1657-1662
    • Pan, C.1    Yu, J.2    Zhou, Y.3    Wang, Z.4    Zhou, M.-M.5
  • 46
    • 0028197129 scopus 로고
    • Isolation and synthesis of 3,4-bis(indol-3-yl)pyrrole-2,5-dicarboxylic acid derivatives from the slime mould Lycogala epidendrum
    • Fröde, R.; Hinze, C.; Josten, I.; Schmidt, B.; Steffan, B.; Steglich, W. Isolation and synthesis of 3,4-bis(indol-3-yl)pyrrole-2,5-dicarboxylic acid derivatives from the slime mould Lycogala epidendrum. Tetrahedron Lett., 1994, 35, 1689-1690.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 1689-1690
    • Fröde, R.1    Hinze, C.2    Josten, I.3    Schmidt, B.4    Steffan, B.5    Steglich, W.6
  • 47
    • 0028211508 scopus 로고
    • Three novel dimethyl pyrroledicarboxylate, lycogarubins A-C, from the myxomycetes lycogala epidendrum
    • Hashimoto, T.; Yasuda, A.; Akazawa, K.; Takaoka, S.; Tori, M.; Asakawa, Y. Three novel dimethyl pyrroledicarboxylate, lycogarubins A-C, from the myxomycetes lycogala epidendrum. Tetrahedron Lett., 1994, 35, 2559-2560.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 2559-2560
    • Hashimoto, T.1    Yasuda, A.2    Akazawa, K.3    Takaoka, S.4    Tori, M.5    Asakawa, Y.6
  • 48
    • 28544449005 scopus 로고    scopus 로고
    • Enzymatic generation of the chromopyrrolic acid scaffold of rebeccamycin by the tandem action of RebO and RebD
    • Howard-Jones, A.R.; Walsh, C.T. Enzymatic generation of the chromopyrrolic acid scaffold of rebeccamycin by the tandem action of RebO and RebD. Biochemistry, 2005, 44, 15652-15663.
    • (2005) Biochemistry , vol.44 , pp. 15652-15663
    • Howard-Jones, A.R.1    Walsh, C.T.2
  • 50
    • 33947504772 scopus 로고    scopus 로고
    • Synthesis of simple 3,4- diarylpyrrole- 2,5-dicarboxylic acids and lukianol a by oxidative condensation of 3-arylpyruvic acids with ammonia
    • Hinze, C.; Kreipl, A.; Terpin, A.; Steglich, W. Synthesis of simple 3,4- diarylpyrrole- 2,5-dicarboxylic acids and lukianol a by oxidative condensation of 3-arylpyruvic acids with ammonia. Synthesis, 2007, 608612.
    • (2007) Synthesis , pp. 608612
    • Hinze, C.1    Kreipl, A.2    Terpin, A.3    Steglich, W.4
  • 51
    • 0034699702 scopus 로고    scopus 로고
    • New and efficient synthesis of 2,2- disubstituted-3,4-dihydro-2H-1-benzopyrans
    • Yadav, J.S.; Reddy, B.V.S.; Hashim, S.R.A new and efficient synthesis of 2,2- disubstituted-3,4-dihydro-2H-1-benzopyrans. J. Chem. Soc., Perkin Trans. 1, 2000, 3082-3084.
    • (2000) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 3082-3084
    • Yadav, J.S.1    Reddy, B.V.S.2    Hashim, S.R.A.3
  • 52
    • 0036015093 scopus 로고    scopus 로고
    • Elemental iodine catalyzed[4 + 2] cycloaddition reactions of o-quinomethanes: An efficient synthesis of trans-fused pyrano[3,2-c]benzopyrans
    • Yadav, J.S.; Reddy, B.V.S.; Rao, C.V.; Rao, K.V. Elemental iodine catalyzed[4 + 2] cycloaddition reactions of o-quinomethanes: an efficient synthesis of trans-fused pyrano[3,2-c]benzopyrans. J. Chem. Soc., Perkin Trans. 1, 2002, 1401-1404.
    • (2002) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1401-1404
    • Yadav, J.S.1    Reddy, B.V.S.2    Rao, C.V.3    Rao, K.V.4
  • 53
    • 8644234920 scopus 로고    scopus 로고
    • An efficient, high yield protocol for the one-pot synthesis of dihydropyrimidin- 2(1H)-ones catalyzed by iodine
    • Bhosale, R.S.; Bhosale, S.V.; Bhosale, S.V.; Wang, T.; Zubaidha, P.K. An efficient, high yield protocol for the one-pot synthesis of dihydropyrimidin- 2(1H)-ones catalyzed by iodine. Tetrahedron Lett., 2004, 45, 9111-9113.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 9111-9113
    • Bhosale, R.S.1    Bhosale, S.V.2    Bhosale, S.V.3    Wang, T.4    Zubaidha, P.K.5
  • 54
    • 4544226835 scopus 로고    scopus 로고
    • Iodine catalyzed one-pot synthesis of 3,4- dihydropyrimidin- 2(1H)-ones and thiones: A simple and efficient procedure for the biginelli reaction
    • Srinivas, K.V.S.; Das, B. Iodine catalyzed one-pot synthesis of 3,4- dihydropyrimidin- 2(1H)-ones and thiones: a simple and efficient procedure for the biginelli reaction. Synthesis, 2004, 2091-2093.
    • (2004) Synthesis , pp. 2091-2093
    • Srinivas, K.V.S.1    Das, B.2
  • 55
    • 12344333687 scopus 로고    scopus 로고
    • Three component condensations catalyzed by iodine-alumina for the synthesis of substituted 3,4- dihydropyrimidin-2(1H)-ones under microwave irradiation and solvent-free conditions
    • Saxena, I.; Borah, D.C.; Sarma, J.C. Three component condensations catalyzed by iodine-alumina for the synthesis of substituted 3,4- dihydropyrimidin-2(1H)-ones under microwave irradiation and solvent-free conditions. Tetrahedron Lett., 2005, 46, 1159-1160.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 1159-1160
    • Saxena, I.1    Borah, D.C.2    Sarma, J.C.3
  • 56
    • 22544457892 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed one-pot synthesis of 4-substituted-1,4-dihydropyridine derivatives via Hantzsch reaction
    • Ko, S.; Sastry, M.N.V.; Lin, C.; Yao, C. Molecular iodine-catalyzed one-pot synthesis of 4-substituted-1,4-dihydropyridine derivatives via Hantzsch reaction. Tetrahedron Lett., 2005, 46, 5771-5774.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 5771-5774
    • Ko, S.1    Sastry, M.N.V.2    Lin, C.3    Yao, C.4
  • 57
    • 15444362350 scopus 로고    scopus 로고
    • Iodine-catalysed bohlmann-rahtz cyclodehydration reactions
    • Bagley, M.C.; Glover, C.; Chevis, D. Iodine-catalysed bohlmann-rahtz cyclodehydration reactions. Synlett, 2005, 649-651.
    • (2005) Synlett , pp. 649-651
    • Bagley, M.C.1    Glover, C.2    Chevis, D.3
  • 58
    • 0036882396 scopus 로고    scopus 로고
    • Irreversible inhibitors of serine, cysteine, and threonine proteases
    • Powers, J.C.; Asgian, J.L.; Ekici, O.-D.; James, K.E. Irreversible inhibitors of serine, cysteine, and threonine proteases. Chem. Rev., 2002, 102, 4639-4750.
    • (2002) Chem. Rev. , vol.102 , pp. 4639-4750
    • Powers, J.C.1    Asgian, J.L.2    Ekici, O.-D.3    James, K.E.4
  • 59
    • 10744221565 scopus 로고    scopus 로고
    • Synthesis of new 3- alkoxy-7- amino-4-chloro-isocoumarin derivatives as new??-amyloid peptide production inhibitors and their activities on various classes of protease
    • Bihel, F.; Quelever, G.; Lelouard, H.; Petit, A.; Alves da Costa, C.; Pourquie, O.; Checler, F.; Thellend, A.; Pierre, P.; Kraus, J.-L. Synthesis of new 3- alkoxy-7- amino-4-chloro-isocoumarin derivatives as new??-amyloid peptide production inhibitors and their activities on various classes of protease. Bioorg. Med. Chem., 2003, 11, 3141-3152.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 3141-3152
    • Bihel, F.1    Quelever, G.2    Lelouard, H.3    Petit, A.4    Alves da Costa, C.5    Pourquie, O.6    Checler, F.7    Thellend, A.8    Pierre, P.9    Kraus, J.-L.10
  • 61
    • 25144459042 scopus 로고    scopus 로고
    • Synthesis of 4-halophosphaisocoumarins via halocyclization of 2-(1-alkynyl)phenylphosphonates
    • Peng, A.-Y.; Ding, Y.-X. Synthesis of 4-halophosphaisocoumarins via halocyclization of 2-(1-alkynyl)phenylphosphonates. Tetrahedron, 2005, 61, 10303-10308.
    • (2005) Tetrahedron , vol.61 , pp. 10303-10308
    • Peng, A.-Y.1    Ding, Y.-X.2
  • 62
    • 34547938472 scopus 로고    scopus 로고
    • Iodine-promoted prins cyclization of ketones-a facile synthesis of spirocyclic-4-iodo-tetrahydropyrans and 5,6-dihydro-2H-pyrans
    • Yadav, J.S.; Reddy, B.V.S.; Hari Krishna, V.; Swamy, T.; Narayana Kumar, G.G.K.S. Iodine-promoted prins cyclization of ketones-a facile synthesis of spirocyclic-4-iodo-tetrahydropyrans and 5,6-dihydro-2H-pyrans. Can. J. Chem., 2007, 85, 412.
    • (2007) Can. J. Chem. , vol.85 , pp. 412
    • Yadav, J.S.1    Reddy, B.V.S.2    Hari, K.V.3    Swamy, T.4    Narayana Kumar, G.G.K.S.5
  • 64
    • 76449107018 scopus 로고    scopus 로고
    • Simple synthesis of functionalized 3-bromocoumarins by a one-pot three-component reaction
    • Audisio, D., Messaoudi, S., Brion, J.D., Alami, M. A simple synthesis of functionalized 3-bromocoumarins by a one-pot three-component reaction. Eur. J. Org. Chem., 2010, 1046-1051
    • (2010) Eur. J. Org. Chem. , pp. 1046-1051
    • Audisio, D.1    Messaoudi, S.2    Brion, J.D.3    Alami, M.A.4
  • 66
    • 0033694467 scopus 로고    scopus 로고
    • 1,8- Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino)[ 1,2,4]triazolo[4,3- a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
    • Roma, G.; Braccio, M.D.; Grossi, G.; Mattioli, F.; Ghia, M. 1,8- Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino)[ 1,2,4]triazolo[4,3- a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities. Eur. J. Med. Chem., 2000, 35, 1021-1035.
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1021-1035
    • Roma, G.1    Braccio, M.D.2    Grossi, G.3    Mattioli, F.4    Ghia, M.5
  • 67
    • 0026420864 scopus 로고
    • New conjugated polyanthrazolines containing thiophene moieties in the main chain
    • Aggarwal, A.K.; Jenekhe, S.A. New conjugated polyanthrazolines containing thiophene moieties in the main chain. Macromolecules, 1991, 24, 6806-6808.
    • (1991) Macromolecules , vol.24 , pp. 6806-6808
    • Aggarwal, A.K.1    Jenekhe, S.A.2
  • 68
    • 0033517645 scopus 로고    scopus 로고
    • Electroluminescence and photophysical properties of polyquinolines
    • Zhang, X.; Shetty, A.S.; Jenekhe, S.A. Electroluminescence and photophysical properties of polyquinolines. Macromolecules, 1999, 32, 7422-7429.
    • (1999) Macromolecules , vol.32 , pp. 7422-7429
    • Zhang, X.1    Shetty, A.S.2    Jenekhe, S.A.3
  • 69
    • 0035833878 scopus 로고    scopus 로고
    • New Conjugated polymers with donoracceptor architectures: Synthesis and photophysics of carbazole??quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer
    • Jenekhe, S.A.; Lu, L.; Alam, M.M. New Conjugated polymers with donoracceptor architectures: synthesis and photophysics of carbazole??quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer. Macromolecules, 2001, 34, 7315-7324.
    • (2001) Macromolecules , vol.34 , pp. 7315-7324
    • Jenekhe, S.A.1    Lu, L.2    Alam, M.M.3
  • 70
    • 0042730088 scopus 로고    scopus 로고
    • Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas
    • Du, W.; Curran, D.P. Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas. Org. Lett., 2003, 5, 1765-1768.
    • (2003) Org. Lett. , vol.5 , pp. 1765-1768
    • Du, W.1    Curran, D.P.2
  • 71
    • 0001651959 scopus 로고    scopus 로고
    • Preparation of polyfunctional heterocycles using highly functionalized aminated arylmagnesium reagents as versatile scaffolds
    • Lindsay, D.M.; Dohle, W.; Jensen, A.E.; Kopp, F.; Knochel, P. Preparation of polyfunctional heterocycles using highly functionalized aminated arylmagnesium reagents as versatile scaffolds. Org. Lett., 2002, 4,1819-1822.
    • (2002) Org. Lett. , vol.4 , pp. 1819-1822
    • Lindsay, D.M.1    Dohle, W.2    Jensen, A.E.3    Kopp, F.4    Knochel, P.5
  • 72
    • 0034727305 scopus 로고    scopus 로고
    • Doebner-miller synthesis in a twophase system: Practical preparation of quinolines
    • Matsugi, M.; Tabusa, F.; Minamikawa, J. Doebner-miller synthesis in a twophase system: practical preparation of quinolines. Tetrahedron Lett., 2000, 41, 8523-8525.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8523-8525
    • Matsugi, M.1    Tabusa, F.2    Minamikawa, J.3
  • 73
    • 0037462413 scopus 로고    scopus 로고
    • Highly regioselective friedländer annulations with unmodified ketones employing novel amine catalysts: Syntheses of 2- substituted quinolines, 1,8-naphthyridines, and related heterocycles
    • Dormer, P.G.; Eng, K.K.; Farr, R.N.; Humphrey, G.R.; McWilliams, J.C.; Reider, P.J.; Sager, J.W.; Volante, R.P. Highly regioselective friedländer annulations with unmodified ketones employing novel amine catalysts: syntheses of 2- substituted quinolines, 1,8-naphthyridines, and related heterocycles. J. Org. Chem., 2003, 68, 467-477.
    • (2003) J. Org. Chem. , vol.68 , pp. 467-477
    • Dormer, P.G.1    Eng, K.K.2    Farr, R.N.3    Humphrey, G.R.4    McWilliams, J.C.5    Reider, P.J.6    Sager, J.W.7    Volante, R.P.8
  • 74
    • 0031849052 scopus 로고    scopus 로고
    • Friedländer synthesis of substituted quinolines from N-pivaloylanilines
    • Ubeda, J.I.; Villacampa, M.; Avendano, C. Friedländer synthesis of substituted quinolines from N-pivaloylanilines. Synthesis, 1998, 1176-1180.
    • (1998) Synthesis , pp. 1176-1180
    • Ubeda, J.I.1    Villacampa, M.2    Avendano, C.3
  • 75
    • 33645675145 scopus 로고    scopus 로고
    • Molecular iodine: A highly efficient catalyst in the synthesis of quinolines via Friedländer annulation
    • Xia, W.J.; Gao, H.-G.K. Molecular iodine: a highly efficient catalyst in the synthesis of quinolines via Friedländer annulation. Org. Biomol. Chem., 2006, 4, 126-129.
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 126-129
    • Xia, W.J.1    Gao, H.-G.K.2
  • 76
    • 75849139207 scopus 로고    scopus 로고
    • Molecular iodine: A versatile catalyst for the synthesis of 2-aryl-2,3-dihydroquinolin-4(1H)-ones
    • 2777-2278
    • Wu, L.; Niu, B.; Li, W.; Yan, F. Molecular iodine: a versatile catalyst for the synthesis of 2-aryl-2,3-dihydroquinolin-4(1H)-ones. Bull. Korean Chem. Soc., 2009, 30, 2777-2278.
    • (2009) Bull. Korean Chem. Soc. , vol.30
    • Wu, L.1    Niu, B.2    Li, W.3    Yan, F.4
  • 80
    • 20044380751 scopus 로고    scopus 로고
    • Aromatization of 1,4-dihydropyridines with selenium dioxide
    • Cai, X.; Yang, H.; Zhang, G. Aromatization of 1,4-dihydropyridines with selenium dioxide. Can. J. Chem., 2005, 83, 273-275.
    • (2005) Can. J. Chem. , vol.83 , pp. 273-275
    • Cai, X.1    Yang, H.2    Zhang, G.3
  • 81
    • 46249102666 scopus 로고    scopus 로고
    • Molecular iodinecatalyzed one- pot synthesis of some new Hantzsch 1,4-dihydropyridines at ambient temperature
    • Akbari, J.D.; Tala, S.D.; Dhaduk, M.F.; Joshi, H.S. Molecular iodinecatalyzed one- pot synthesis of some new Hantzsch 1,4-dihydropyridines at ambient temperature. Arkivoc, 2008 (xii) 126-135.
    • (2008) Arkivoc , Issue.xii , pp. 126-135
    • Akbari, J.D.1    Tala, S.D.2    Dhaduk, M.F.3    Joshi, H.S.4
  • 82
    • 0036015093 scopus 로고    scopus 로고
    • Elemental iodine catalyzed[ 4 -2] cycloaddition reactions of o-quinomethanes: An efficient synthesis of trans-fused pyrano[3,2-c]benzopyrans
    • Yadav, J.S.; Reddy, B.V.S.; Rao, C.V.; Rao, K.V. Elemental iodine catalyzed[ 4 -2] cycloaddition reactions of o-quinomethanes: an efficient synthesis of trans-fused pyrano[3,2-c]benzopyrans. J. Chem. Soc. Perkin Trans. 1, 2002, 1401-1404.
    • (2002) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1401-1404
    • Yadav, J.S.1    Reddy, B.V.S.2    Rao, C.V.3    Rao, K.V.4
  • 83
    • 47049125207 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed diastereoselective synthesis of cis-fused pyranobenzopyrans and furanobenzopyrans
    • Wang, J.; Xu, F.-X.; Lin, X.-F.; Wang, Y.-G. Molecular iodine-catalyzed diastereoselective synthesis of cis-fused pyranobenzopyrans and furanobenzopyrans. Tetrahedron Lett., 2008, 49, 5208-5210.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 5208-5210
    • Wang, J.1    Xu, F.-X.2    Lin, X.-F.3    Wang, Y.-G.4
  • 84
    • 0035796959 scopus 로고    scopus 로고
    • A new molecular iodine- catalyzed thioketalization of carbonyl compounds: Selectivity and scope
    • Samajdar, S.; Basu, M.K.; Becker, F.F.; Banik, B.K. A new molecular iodine- catalyzed thioketalization of carbonyl compounds: selectivity and scope. Tetrahedron Lett., 2001, 42, 4425-4427.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4425-4427
    • Samajdar, S.1    Basu, M.K.2    Becker, F.F.3    Banik, B.K.4
  • 85
    • 0035538660 scopus 로고    scopus 로고
    • Highly efficient dithioacetalization of carbonyl compounds catalyzed with iodine supported on neutral alumina
    • Nabajyoti, D.; Sarma, J.C. Highly efficient dithioacetalization of carbonyl compounds catalyzed with iodine supported on neutral alumina. Chem. Lett., 2001, 30, 794-796.
    • (2001) Chem. Lett. , vol.30 , pp. 794-796
    • Nabajyoti, D.1    Sarma, J.C.2
  • 86
    • 38949208840 scopus 로고    scopus 로고
    • One-pot synthesis of 2-(1- alkyl/aralkyl-1H-benzimidazole-2-yl)-quinoxaline derivatives using molecular iodine
    • Dubey, P.K.; Prasada Reddy, P.V.V.; Srinivas, K. One-pot synthesis of 2-(1- alkyl/aralkyl-1H-benzimidazole-2-yl)-quinoxaline derivatives using molecular iodine. Synth. Commun., 2008, 38, 613-618.
    • (2008) Synth. Commun. , vol.38 , pp. 613-618
    • Dubey, P.K.1    Prasada Reddy, P.V.V.2    Srinivas, K.3
  • 87
    • 33751335837 scopus 로고    scopus 로고
    • Indolocarbazole natural products: Occurrence, biosynthesis, and biological activity
    • Sanchez, C.; Mendez, C.; Salas, J. A. Indolocarbazole natural products: occurrence, biosynthesis, and biological activity. Nat. Prod. Rep., 2006, 23, 1007-1045.
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 1007-1045
    • Sanchez, C.1    Mendez, C.2    Salas, J.A.3
  • 88
    • 85196230467 scopus 로고    scopus 로고
    • Heterocyclic analogues of carbazole alkaloids
    • Krisch, G.H. Heterocyclic analogues of carbazole alkaloids. Curr. Org. Chem., 2000, 4, 765-777.
    • (2000) Curr. Org. Chem. , vol.4 , pp. 765-777
    • Krisch, G.H.1
  • 89
    • 38849154166 scopus 로고    scopus 로고
    • A facile synthesis of 6,12-disubstituted 5,7- dihydroindolo[ 2,3-b]carbazoles from the reaction of 1H-indole and aldehydes catalyzed by molecular iodine
    • Deb, M.L.; Bhuyan, P.J. A facile synthesis of 6,12-disubstituted 5,7- dihydroindolo[ 2,3-b]carbazoles from the reaction of 1H-indole and aldehydes catalyzed by molecular iodine. Synthesis, 2008, 286-292.
    • (2008) Synthesis , pp. 286-292
    • Deb, M.L.1    Bhuyan, P.J.2
  • 90
    • 58049176368 scopus 로고    scopus 로고
    • Facile and general method for the synthesis of 6,12-diaryl-5,11-dihydroindolo[3,2- b]carbazoles
    • Gu, R.; Van Snick, S.; Robeyns, K.; Van Meervelt, L.; Dehaen, W. A facile and general method for the synthesis of 6,12-diaryl-5,11-dihydroindolo[3,2- b]carbazoles. Org. Biomol. Chem., 2009, 7, 380-385.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 380-385
    • Gu, R.1    van Snick, S.2    Robeyns, K.3    van Meervelt, L.4    Dehaen, W.A.5
  • 91
    • 39749105300 scopus 로고    scopus 로고
    • An efficient method for the synthesis of indolo[3,2- b]carbazoles from 3,3'-bis(indolyl)methanes catalyzed by molecular iodine
    • Deb, M.L.; Bhuyan, P.J. An efficient method for the synthesis of indolo[3,2- b]carbazoles from 3,3'-bis(indolyl)methanes catalyzed by molecular iodine. Synlett, 2008, 325-328.
    • (2008) Synlett , pp. 325-328
    • Deb, M.L.1    Bhuyan, P.J.2
  • 92
    • 0041659909 scopus 로고    scopus 로고
    • Synthesis and sntimicrobial activities of some novel quinoxalinone derivatives
    • Ali, M.M.; Ismail, M.M.F.; EI-Gabby, M.S.A.; Zahran, M.A.; Ammar, T.A.; Synthesis and sntimicrobial activities of some novel quinoxalinone derivatives. Molecules, 2000, 5, 864-873.
    • (2000) Molecules , vol.5 , pp. 864-873
    • Ali, M.M.1    Ismail, M.M.F.2    Ei-Gabby, M.S.A.3    Zahran, M.A.4    Ammar, T.A.5
  • 93
    • 0025306964 scopus 로고
    • 4- Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants
    • Sarges, R.; Howard, H.R.; Browne, R.C.; Label, L.A.; Seymour, P.A. 4- Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. J. Med. Chem., 1990, 33, 2240-2254.
    • (1990) J. Med. Chem. , vol.33 , pp. 2240-2254
    • Sarges, R.1    Howard, H.R.2    Browne, R.C.3    Label, L.A.4    Seymour, P.A.5
  • 95
    • 0032840116 scopus 로고    scopus 로고
    • Recognition elements that determine affinity and sequence-specific binding to DNA of 2QN, a biosynthetic bis-quinoline analogue of echinomycin
    • Bailly, C.; Echepare, S.; Gago, F.; Waring, M. Recognition elements that determine affinity and sequence-specific binding to DNA of 2QN, a biosynthetic bis-quinoline analogue of echinomycin. Anti-Cancer Drug Des., 1999, 15, 291-303.
    • (1999) Anti-Cancer Drug Des. , vol.15 , pp. 291-303
    • Bailly, C.1    Echepare, S.2    Gago, F.3    Waring, M.4
  • 96
    • 23744463590 scopus 로고    scopus 로고
    • Molecular iodine: A powerful catalyst for the easy and efficient synthesis of quinoxalines
    • More, S.V.; Sastry, M.N.V.; Wang, C.-C.; Yao, C.-F. Molecular iodine: a powerful catalyst for the easy and efficient synthesis of quinoxalines. Tetrahedron Lett., 2005, 46, 6345.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 6345
    • More, S.V.1    Sastry, M.N.V.2    Wang, C.-C.3    Yao, C.-F.4
  • 97
    • 24944446763 scopus 로고    scopus 로고
    • An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst
    • Bhosale, R.S.; Sarda, S.R.; Ardhapure, S.S.; Jadhav, W.N.; Bhusare, S.R.; Pawara, R.P. An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst. Tetrahedron Lett., 2005, 46, 7183-7186.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7183-7186
    • Bhosale, R.S.1    Sarda, S.R.2    Ardhapure, S.S.3    Jadhav, W.N.4    Bhusare, S.R.5    Pawara, R.P.6
  • 98
    • 0000899922 scopus 로고
    • The synthesis and properties of 6- chloropurine and purine
    • Bendich, A.; Russell, P.J.; Fox, J.J. The synthesis and properties of 6- chloropurine and purine. J. Am. Chem. Soc., 1954, 76, 6073-6077.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 6073-6077
    • Bendich, A.1    Russell, P.J.2    Fox, J.J.3
  • 99
    • 32044468685 scopus 로고    scopus 로고
    • Synthesis of some novel pyrazolo[3,4-d]pyrimidine derivatives as potential antimicrobial agents
    • Holla, B.S.; Mahalinga, M.; Karthikeyan, M.S.; Akberali, P.M.; Shetty, N.S. Synthesis of some novel pyrazolo[3,4-d]pyrimidine derivatives as potential antimicrobial agents. Bioorg. Med. Chem., 2005, 14, 2040-2047.
    • (2005) Bioorg. Med. Chem. , vol.14 , pp. 2040-2047
    • Holla, B.S.1    Mahalinga, M.2    Karthikeyan, M.S.3    Akberali, P.M.4    Shetty, N.S.5
  • 101
    • 33947602611 scopus 로고    scopus 로고
    • Synthesis and herbicidal activity of novel pyrazolo[3,4-d]pyrimidin-4-one derivatives containing aryloxyphenoxypropionate moieties
    • Liu, H.; Wang, H.Q.; Liu, Z.J. Synthesis and herbicidal activity of novel pyrazolo[3,4-d]pyrimidin-4-one derivatives containing aryloxyphenoxypropionate moieties. Bioorg. Med. Chem. Lett., 2007, 17, 2203-2209.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 2203-2209
    • Liu, H.1    Wang, H.Q.2    Liu, Z.J.3
  • 103
    • 44649126044 scopus 로고    scopus 로고
    • Iodine as a mild and versatile reagent for the synthesis of 1,3- dioxane derivatives via the Prins reaction
    • Yadav, J.S.; Reddy, B.V.S.; Gopal, A.V.H.; Kumar, G.G.K.S.N.; Madavi, C.; Kunwar, A.C. Iodine as a mild and versatile reagent for the synthesis of 1,3- dioxane derivatives via the Prins reaction. Tetrahedron Lett., 2008, 49, 4420-4423.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 4420-4423
    • Yadav, J.S.1    Reddy, B.V.S.2    Gopal, A.V.H.3    Kumar, G.G.K.S.N.4    Madavi, C.5    Kunwar, A.C.6
  • 104
    • 41949093836 scopus 로고    scopus 로고
    • Gallium iodide/iodine as a versatile reagent for the aza- Prins cyclization: An expeditious synthesis of 4-iodopiperidines
    • Yadav, J.S.; Reddy, B.V.S.; Chaya, D.N.; Kumar, G.G.K.S.N.; Aravind, S.; Kunwar, A.C.; Madavi, C. Gallium iodide/iodine as a versatile reagent for the aza- Prins cyclization: an expeditious synthesis of 4-iodopiperidines. Tetrahedron Lett., 2008, 49, 3330-3334.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 3330-3334
    • Yadav, J.S.1    Reddy, B.V.S.2    Chaya, D.N.3    Kumar, G.G.K.S.N.4    Aravind, S.5    Kunwar, A.C.6    Madavi, C.7
  • 105
    • 33845342566 scopus 로고    scopus 로고
    • Iodinecatalyzed synthesis of novel Hantzsch N-hydroxyethyl 1,4-dihydropyridines under mild conditions
    • Zolfigol, M.A.; Salehi, P.; Khorramabadi-Zad, A.; Shayegh, M. Iodinecatalyzed synthesis of novel Hantzsch N-hydroxyethyl 1,4-dihydropyridines under mild conditions. J. Mol. Catal. A:Chem., 2007, 261, 88-92.
    • (2007) J. Mol. Catal. A:Chem. , vol.261 , pp. 88-92
    • Zolfigol, M.A.1    Salehi, P.2    Khorramabadi-Zad, A.3    Shayegh, M.4
  • 106
    • 33645879237 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed one-pot synthesis of substituted quinolines from imines and aldehydes
    • Lin, X.-F.; Cui, S.-L.; Wang, Y.-G. Molecular iodine-catalyzed one-pot synthesis of substituted quinolines from imines and aldehydes. Tetrahedron Lett., 2006, 47, 3127-3130.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 3127-3130
    • Lin, X.-F.1    Cui, S.-L.2    Wang, Y.-G.3
  • 112
    • 0032998025 scopus 로고    scopus 로고
    • Geiparvarin analogues: Synthesis and anticancer evaluation of -methylidene- -butyrolactonebearing coumarins
    • Chen, Y.L.; Wang, T.C.; Tzeng, C.C.; Chang, N.C. Geiparvarin analogues: synthesis and anticancer evaluation of -methylidene- -butyrolactonebearing coumarins. Helv. Chim. Acta, 1999, 82,191-197.
    • (1999) Helv. Chim. Acta. , vol.82 , pp. 191-197
    • Chen, Y.L.1    Wang, T.C.2    Tzeng, C.C.3    Chang, N.C.4
  • 115
    • 0016697518 scopus 로고
    • The effect of dibenzoxanthenes on the paralyzing action of zoxazolamine
    • Saint-Ruf, G.; Hieu, H.T.; Poupelin, J.P. The effect of dibenzoxanthenes on the paralyzing action of zoxazolamine. Naturwissenschaften, 1975, 62, 584-585.
    • (1975) Naturwissenschaften , vol.62 , pp. 584-585
    • Saint-Ruf, G.1    Hieu, H.T.2    Poupelin, J.P.3
  • 116
    • 0024559378 scopus 로고
    • Xanthene-dye-labelled phosphatidylethanolamines as probes of interfacial pH Studies In Phospholipid Vesicles
    • Knight, C.G.; Stephens, T. Xanthene-dye-labelled phosphatidylethanolamines as probes of interfacial pH. Studies in phospholipid vesicles. Biochem. J., 1989, 258, 683-687.
    • (1989) Biochem. J. , vol.258 , pp. 683-687
    • Knight, C.G.1    Stephens, T.2
  • 117
    • 0012739850 scopus 로고
    • Structural studies on santalin permethyl ether
    • Ravindranath, B.; Seshadri, T.R. Structural studies on santalin permethyl ether. Phytochemistry, 1973, 12, 2781-2788.
    • (1973) Phytochemistry , vol.12 , pp. 2781-2788
    • Ravindranath, B.1    Seshadri, T.R.2
  • 118
    • 85047673233 scopus 로고
    • Novel yellow pigment from Pterocarpus santalinus. Biogenetic Hypothesis For Santalin Analogs
    • Kinjo, J.; Uemura, H.; Nohara, T.; Yamashita, M.; Marubayashi, N.; Yoshihira, K. Novel yellow pigment from Pterocarpus santalinus: Biogenetic hypothesis for santalin analogs. Tetrahedron Lett., 1995, 36, 5599-5602.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5599-5602
    • Kinjo, J.1    Uemura, H.2    Nohara, T.3    Yamashita, M.4    Marubayashi, N.5    Yoshihira, K.6
  • 119
    • 33746025668 scopus 로고    scopus 로고
    • Iodine catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-Hdibenzo[ a,j]xanthenes
    • Das, B.; Ravikanth, B.; Ramu, R.; Laxminarayana, K.; Vittal Rao, B. Iodine catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-Hdibenzo[ a,j]xanthenes. J. Mol. Catal. A: Chem., 2006, 255, 74.
    • (2006) J. Mol. Catal. A: Chem. , vol.255 , pp. 74
    • Das, B.1    Ravikanth, B.2    Ramu, R.3    Laxminarayana, K.4    Vittal Rao, B.5
  • 120
    • 33846240529 scopus 로고    scopus 로고
    • Molecular iodine catalyzed synthesis of aryl-14H- dibenzo[a, j]xanthenes under solvent-free condition
    • Pasha, M.A.; Jayashankara, V.P. Molecular iodine catalyzed synthesis of aryl-14H- dibenzo[a, j]xanthenes under solvent-free condition. Bioorg. Med. Chem. Lett., 2007, 17, 621-623.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 621-623
    • Pasha, M.A.1    Jayashankara, V.P.2
  • 121
    • 43449132077 scopus 로고    scopus 로고
    • An efficient, metal-free, room temperature aromatization of Hantzsch-1,4-dihydropyridines with urea- hydrogen peroxide adduct, catalyzed by molecular iodine
    • Filipan-Litvić, M.; Litvić, M.; Vinković, V. An efficient, metal-free, room temperature aromatization of Hantzsch-1,4-dihydropyridines with urea- hydrogen peroxide adduct, catalyzed by molecular iodine. Tetrahedron, 2008, 64, 5649-5656.
    • (2008) Tetrahedron , vol.64 , pp. 5649-5656
    • Filipan-Litvić, M.1    Litvić, M.2    Vinković, V.3
  • 122
    • 17844406371 scopus 로고    scopus 로고
    • Allylation and cyanation of aza-aromatics activated by chloroformate and a catalytic amount of iodine
    • Yadav, J.S.; Reddy, B.V.S.; Sirnivas, M.; Sathaiah, K. Allylation and cyanation of aza-aromatics activated by chloroformate and a catalytic amount of iodine. Tetrahedron Lett., 2005, 46, 3489-3492.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 3489-3492
    • Yadav, J.S.1    Reddy, B.V.S.2    Sirnivas, M.3    Sathaiah, K.4
  • 123
    • 35548969262 scopus 로고    scopus 로고
    • Iodine as a mild, efficient, and cost-effective reagent for the synthesis of cis-1-oxo-1,2,3,4- tetrahydroisoquinoline-4-carboxylic acids
    • Yadav, J.S.; Reddy, B.V.S.; Reddy, A.R.; Narsaiah, A.V. Iodine as a mild, efficient, and cost-effective reagent for the synthesis of cis-1-oxo-1,2,3,4- tetrahydroisoquinoline-4-carboxylic acids. Synthesis, 2007, 3191-3194.
    • (2007) Synthesis , pp. 3191-3194
    • Yadav, J.S.1    Reddy, B.V.S.2    Reddy, A.R.3    Narsaiah, A.V.4
  • 124
    • 19944401847 scopus 로고    scopus 로고
    • Molecular-iodine-catalyzed one-pot synthesis of 1,5- benzodiazepine Derivatives under solvent-free conditions
    • Chen, W.; Lu, J. Molecular-iodine-catalyzed one-pot synthesis of 1,5- benzodiazepine Derivatives under solvent-free conditions. Synlett, 2005, 1337-1339.
    • (2005) Synlett , pp. 1337-1339
    • Chen, W.1    Lu, J.2
  • 125
    • 33947122585 scopus 로고    scopus 로고
    • Molecular iodine: A highly efficient catalyst for the synthesis of 7-arylbenzopyrano[1,3]diazepines in non-protic solvents
    • Kidwai, M.; Bansal, V.; Mothsra, P. Molecular iodine: A highly efficient catalyst for the synthesis of 7-arylbenzopyrano[1,3]diazepines in non-protic solvents. J. Mol. Catal. A: Chem., 2007, 266, 43-46.
    • (2007) J. Mol. Catal. A: Chem. , vol.266 , pp. 43-46
    • Kidwai, M.1    Bansal, V.2    Mothsra, P.3
  • 126
    • 70449367271 scopus 로고    scopus 로고
    • Iodocyclization of N-[2- (methylthio) phenyl]propiolamides: Selective synthesis of 3-iodo-1,5- benzothiazepin- 4-ones
    • Han Jiang, T.-S.; Zhang, X.-G.; Li, J.-H. Iodocyclization of N-[2- (methylthio) phenyl]propiolamides: selective synthesis of 3-iodo-1,5- benzothiazepin- 4-ones. Synthesis, 2009, 3029-3038.
    • (2009) Synthesis , pp. 3029-3038
    • Han Jiang, T.-S.1    Zhang, X.-G.2    Li, J.-H.3
  • 127
    • 0028785689 scopus 로고
    • An improved synthesis of 2,2- disubstituted-1,2-dihydroquinolines and their conversion to 3-chloro-2,2- disubstituted-tetrahydroquinolines
    • Williamson, N.M.; March, D.R.; Ward, A.D. An improved synthesis of 2,2- disubstituted-1,2-dihydroquinolines and their conversion to 3-chloro-2,2- disubstituted-tetrahydroquinolines. Tetraheron Lett., 1995, 36, 7721-7724.
    • (1995) Tetraheron Lett , vol.36 , pp. 7721-7724
    • Williamson, N.M.1    March, D.R.2    Ward, A.D.3
  • 128
    • 0026749637 scopus 로고
    • 2-Carboxytetrahydroquinolines. Conformational and stereochemical requirements for antagonism of the glycine site on the N-methyl-D-aspartate (NMDA) receptor
    • Carling, R.W.; Leeson, P.D.; Moseley, A.M.; Baker, R.; Foster, A.C.; Grimwood, S.; Kemp, J.A.; Marshall, G.R. 2-Carboxytetrahydroquinolines. Conformational and stereochemical requirements for antagonism of the glycine site on the N-methyl-D-aspartate (NMDA) receptor, J. Med.Chem., 1992, 35, 1942-1953.
    • (1992) J. Med.Chem. , vol.35 , pp. 1942-1953
    • Carling, R.W.1    Leeson, P.D.2    Moseley, A.M.3    Baker, R.4    Foster, A.C.5    Grimwood, S.6    Kemp, J.A.7    Marshall, G.R.8
  • 130
    • 47149098956 scopus 로고    scopus 로고
    • Molecular iodine catalyzed one-pot aza-diels-alder reaction under solvent-free conditions
    • Shen, S.-S.; Ji, S.-J. Molecular iodine catalyzed one-pot aza-diels-alder reaction under solvent-free conditions. Chin. J. Chem., 2008, 26, 935.
    • (2008) Chin. J. Chem. , vol.26 , pp. 935
    • Shen, S.-S.1    Ji, S.-J.2
  • 131
    • 33646767134 scopus 로고    scopus 로고
    • A highly efficient synthesis of 1,2,3,4- tetrahydroquinolines by molecular iodine-catalyzed domino reaction of anilines with cyclic enol ethers
    • Lin, X.-F.; Cui, S.-L.; Wang, Y.-G. A highly efficient synthesis of 1,2,3,4- tetrahydroquinolines by molecular iodine-catalyzed domino reaction of anilines with cyclic enol ethers. Tetrahedron Lett., 2006, 47, 4509-4512.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 4509-4512
    • Lin, X.-F.1    Cui, S.-L.2    Wang, Y.-G.3
  • 132
    • 25444530933 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed imino-diels-alder reactions: Efficient one-pot synthesis of pyrano[3,2-c]quinolines
    • Xia, M.; Lu, Y.-D. Molecular iodine-catalyzed imino-diels-alder reactions: efficient one-pot synthesis of pyrano[3,2-c]quinolines. Synlett, 2005, 2357-2361.
    • (2005) Synlett , pp. 2357-2361
    • Xia, M.1    Lu, Y.-D.2
  • 133
    • 0038356810 scopus 로고    scopus 로고
    • InCl3-catalyzed[3 + 2] cycloaddition reactions: A facile synthesis of trans-dihydrobenzofurans and substituted cyclobutane derivatives
    • Yadav, J.S.; Reddy, B.V.S.; Kondaji, G. InCl3-catalyzed[3 + 2] cycloaddition reactions: A facile synthesis of trans-dihydrobenzofurans and substituted cyclobutane derivatives. Synthesis, 2003, 1100-1104.
    • (2003) Synthesis , pp. 1100-1104
    • Yadav, J.S.1    Reddy, B.V.S.2    Kondaji, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.