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Volumn 50, Issue 21, 2011, Pages 12271-12275

Environment-friendly bromination of aromatic heterocycles using a bromide-bromate couple in an aqueous medium

Author keywords

[No Author keywords available]

Indexed keywords

ACID ACTIVATION; AQUEOUS CONDITION; AQUEOUS MEDIUM; ELECTRON-RICH; ENVIRONMENT FRIENDLY; GOOD YIELD; HETEROCYCLES; HETEROCYCLIC COMPOUND; IN-SITU; MONOBROMINATION; REACTIVE SPECIES;

EID: 80055035474     PISSN: 08885885     EISSN: 15205045     Source Type: Journal    
DOI: 10.1021/ie2004863     Document Type: Article
Times cited : (18)

References (58)
  • 6
    • 65749105973 scopus 로고    scopus 로고
    • Synthesis of 1,3-diarylated imidazo[1,5-a]pyridines with a combinatorial approach: Metal-catalyzed cross-coupling reactions of 1-halo-3-arylimidazo-[1,5- a]pyridines with arylmetal reagents
    • Shibahara, F.; Yamaguchi, E.; Kitagawa, A.; Imai, A.; Murai, T. Synthesis of 1,3-diarylated imidazo[1,5-a]pyridines with a combinatorial approach: metal-catalyzed cross-coupling reactions of 1-halo-3-arylimidazo-[1,5-a] pyridines with arylmetal reagents Tetrahedron 2009, 65, 5062
    • (2009) Tetrahedron , vol.65 , pp. 5062
    • Shibahara, F.1    Yamaguchi, E.2    Kitagawa, A.3    Imai, A.4    Murai, T.5
  • 7
    • 57649106786 scopus 로고    scopus 로고
    • Efficient total syntheses of louisianins C and D
    • Ching-Yao, C.; Hui-Ming, L.; Ru-Ting, H. Efficient total syntheses of louisianins C and D Tetrahedron 2009, 65, 748
    • (2009) Tetrahedron , vol.65 , pp. 748
    • Ching-Yao, C.1    Hui-Ming, L.2    Ru-Ting, H.3
  • 8
    • 0001606083 scopus 로고    scopus 로고
    • Regiospecific Bromination of 3-Methylindoles with NBS and Its Application to the Concise Synthesis of Optically Active Unusual Tryptophans Present in Marine Cyclic Peptides
    • Liu, R.; Zhang, P.; Gan, T.; Cook, J. M. Regiospecific Bromination of 3-Methylindoles with NBS and Its Application to the Concise Synthesis of Optically Active Unusual Tryptophans Present in Marine Cyclic Peptides J. Org. Chem. 1997, 62, 7447
    • (1997) J. Org. Chem. , vol.62 , pp. 7447
    • Liu, R.1    Zhang, P.2    Gan, T.3    Cook, J.M.4
  • 9
    • 0034997350 scopus 로고    scopus 로고
    • Synthesis and Cytotoxicity Evaluation of Novel Indolylpyrimidines and Indolylpyrazines as Potential Antitumor Agents
    • Jiang, B.; Yang, C.-G.; Xiong, W.-N.; Wang, J. Synthesis and Cytotoxicity Evaluation of Novel Indolylpyrimidines and Indolylpyrazines as Potential Antitumor Agents Bioorg. Med. Chem. 2001, 9, 1149
    • (2001) Bioorg. Med. Chem. , vol.9 , pp. 1149
    • Jiang, B.1    Yang, C.-G.2    Xiong, W.-N.3    Wang, J.4
  • 10
    • 79651470478 scopus 로고    scopus 로고
    • Thermal and Microwave-Assisted Rapid Syntheses of Substituted Imidazo[1,2-a]pyridines under Solvent- and Catalyst-Free Conditions
    • references therein
    • Chunawala, K. C.; Joshi, G.; Suresh, E.; Adimurthy, S. Thermal and Microwave-Assisted Rapid Syntheses of Substituted Imidazo[1,2-a]pyridines Under Solvent- and Catalyst-Free Conditions Synthesis 2011, 635 and references therein
    • (2011) Synthesis , pp. 635
    • Chunawala, K.C.1    Joshi, G.2    Suresh, E.3    Adimurthy, S.4
  • 11
    • 70649089374 scopus 로고    scopus 로고
    • A Novel Method for the Bromination of Thiophenes
    • Arsenyan, P.; Paegle, E.; Belyakov, S. A Novel Method for the Bromination of Thiophenes Tetrahedron Lett. 2010, 51, 205
    • (2010) Tetrahedron Lett. , vol.51 , pp. 205
    • Arsenyan, P.1    Paegle, E.2    Belyakov, S.3
  • 12
    • 43849105598 scopus 로고    scopus 로고
    • Iridium-Catalyzed Borylation of Thiophenes: Versatile, Synthetic Elaboration Founded on Selective C-H Functionalization
    • Chotana, G. A.; Kallepalli, V. A.; Maleczka, R. E., Jr.; Smith, M. R., III. Iridium-Catalyzed Borylation of Thiophenes: Versatile, Synthetic Elaboration Founded on Selective C-H Functionalization Tetrahedron 2008, 64, 6103
    • (2008) Tetrahedron , vol.64 , pp. 6103
    • Chotana, G.A.1    Kallepalli, V.A.2    Maleczka Jr., R.E.3
  • 13
    • 34548760776 scopus 로고    scopus 로고
    • 2: Synthesis and Application of 3,4-Diaryl-2,5- dibromothiophenes
    • 2: Synthesis and Application of 3,4-Diaryl-2,5-dibromothiophenes J. Org. Chem. 2007, 72, 6901
    • (2007) J. Org. Chem. , vol.72 , pp. 6901
    • Dang, Y.1    Chen, Y.2
  • 14
    • 77957140982 scopus 로고    scopus 로고
    • One-Pot Desulfurative-Fluorination-Bromination. Synthesis of 2,5-Dibromo-3-(1,1-difluoroalkyl)thiophenes
    • Turkman, N.; An, L.; Pomerantz, M. One-Pot Desulfurative-Fluorination- Bromination. Synthesis of 2,5-Dibromo-3-(1,1-difluoroalkyl)thiophenes Org. Lett. 2010, 12, 4428
    • (2010) Org. Lett. , vol.12 , pp. 4428
    • Turkman, N.1    An, L.2    Pomerantz, M.3
  • 16
    • 68949113487 scopus 로고    scopus 로고
    • Highly Efficient Borylation Suzuki Coupling Process for 4-Bromo-2-ketothiazoles: Straightforward Access to Micrococcinate and Saramycetate Esters
    • Martin, T.; Laguerre, C.; Hoarau, C.; Marsais, F. Highly Efficient Borylation Suzuki Coupling Process for 4-Bromo-2-ketothiazoles: Straightforward Access to Micrococcinate and Saramycetate Esters Org. Lett. 2009, 11, 3690
    • (2009) Org. Lett. , vol.11 , pp. 3690
    • Martin, T.1    Laguerre, C.2    Hoarau, C.3    Marsais, F.4
  • 17
    • 2042507954 scopus 로고
    • Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
    • Miyaura, N.; Suzuki, A. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds Chem. Rev. 1995, 95, 2457
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 18
    • 0034249671 scopus 로고    scopus 로고
    • The Heck Reaction as a Sharpening Stone of Palladium Catalysis
    • Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis Chem. Rev. 2000, 100, 3009
    • (2000) Chem. Rev. , vol.100 , pp. 3009
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 19
    • 33748647785 scopus 로고
    • Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb
    • Meijere, A.; Meyer, F. E. Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb Angew. Chem., Int. Ed. 1994, 33, 2379
    • (1994) Angew. Chem., Int. Ed. , vol.33 , pp. 2379
    • Meijere, A.1    Meyer, F.E.2
  • 21
    • 78649464701 scopus 로고    scopus 로고
    • Copper- and Solvent-free Sonogashira Coupling Reactions of Aryl Halides with Terminal Alkynes Catalyzed by 1-Phenyl-1,2-propanedione-2-oxime thiosemi-carbazone-Functionalized Polystyrene Resin Supported Pd(II) Complex under Aerobic Conditions
    • Bakherad, M.; Keivanloo, A.; Bahramian, B.; Jajarmi, S. Copper- and Solvent-free Sonogashira Coupling Reactions of Aryl Halides with Terminal Alkynes Catalyzed by 1-Phenyl-1,2-propanedione-2-oxime thiosemi-carbazone- Functionalized Polystyrene Resin Supported Pd(II) Complex under Aerobic Conditions Appl. Catal., A 2010, 390, 135
    • (2010) Appl. Catal., A , vol.390 , pp. 135
    • Bakherad, M.1    Keivanloo, A.2    Bahramian, B.3    Jajarmi, S.4
  • 23
    • 0034712156 scopus 로고    scopus 로고
    • Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates
    • Wolfe, J. P.; Tomori, H.; Sadighi, J. P.; Yin, H.; Buchwald, S. L. Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates J. Org. Chem. 2000, 65, 1158
    • (2000) J. Org. Chem. , vol.65 , pp. 1158
    • Wolfe, J.P.1    Tomori, H.2    Sadighi, J.P.3    Yin, H.4    Buchwald, S.L.5
  • 24
    • 0034682151 scopus 로고    scopus 로고
    • High Turnover Number and Rapid, Room-Temperature Amination of Chloroarenes Using Saturated Carbene Ligands
    • references cited therein
    • Stauffer, S. R.; Lee, S.; Stambuli, J. P.; Hauck, S. I.; Hartwig, J. F. High Turnover Number and Rapid, Room-Temperature Amination of Chloroarenes Using Saturated Carbene Ligands Org. Lett. 2000, 2, 1423 and references cited therein
    • (2000) Org. Lett. , vol.2 , pp. 1423
    • Stauffer, S.R.1    Lee, S.2    Stambuli, J.P.3    Hauck, S.I.4    Hartwig, J.F.5
  • 25
    • 78651383339 scopus 로고    scopus 로고
    • An Investigation of the Bromination of 1,4-dihydropyridine Rings
    • Rorlik, O.; Tashma, Z.; Barzilay, C. M.; Srebnik, M. An Investigation of the Bromination of 1,4-dihydropyridine Rings Tetrahedron Lett. 2011, 52, 757
    • (2011) Tetrahedron Lett. , vol.52 , pp. 757
    • Rorlik, O.1    Tashma, Z.2    Barzilay, C.M.3    Srebnik, M.4
  • 27
    • 34548760776 scopus 로고    scopus 로고
    • 2: Synthesis and Application of 3,4-Diaryl-2,5- dibromothiophenes
    • 2: Synthesis and Application of 3,4-Diaryl-2,5-dibromothiophenes J. Org. Chem. 2007, 72, 6901
    • (2007) J. Org. Chem. , vol.72 , pp. 6901
    • Dang, Y.1    Chen, Y.2
  • 28
    • 77950690807 scopus 로고    scopus 로고
    • The First Total Synthesis of Potent Human Chymase Inhibitor SPF32629B via Regioselective Bromination and O -acylation Strategy
    • Vegi, S. R.; Boovanahalli, S. K.; Mukkanti, B. P. K. The First Total Synthesis of Potent Human Chymase Inhibitor SPF32629B via Regioselective Bromination and O -acylation Strategy Tetrahedron Lett. 2010, 51, 2768
    • (2010) Tetrahedron Lett. , vol.51 , pp. 2768
    • Vegi, S.R.1    Boovanahalli, S.K.2    Mukkanti, B.P.K.3
  • 29
    • 33947317579 scopus 로고    scopus 로고
    • A Facile Nuclear Bromination of Phenols and Anilines using NBS in the Presence of Ammonium Acetate as a Catalyst
    • Das, B.; Venkateswarlu, K.; Majhi, A.; Siddaiah, V.; Reddy, K. R. A Facile Nuclear Bromination of Phenols and Anilines using NBS in the Presence of Ammonium Acetate as a Catalyst J. Mol. Catal. A: Chem. 2007, 267, 30
    • (2007) J. Mol. Catal. A: Chem. , vol.267 , pp. 30
    • Das, B.1    Venkateswarlu, K.2    Majhi, A.3    Siddaiah, V.4    Reddy, K.R.5
  • 30
    • 34249659430 scopus 로고    scopus 로고
    • A Fast and Efficient Bromination of Isoxazoles and Pyrazoles by Microwave Irradiation
    • Li, G.; Kakarla, R.; Gerritz, S. W. A Fast and Efficient Bromination of Isoxazoles and Pyrazoles by Microwave Irradiation Tetrahedron Lett. 2007, 48, 4595
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4595
    • Li, G.1    Kakarla, R.2    Gerritz, S.W.3
  • 31
    • 34548202736 scopus 로고    scopus 로고
    • Regioselective Synthesis of Substituted Pyrrolopyridines Based on Pd(II)-Mediated Cross Coupling and Base Induced Heteroannulation
    • Majumdar, K. C.; Mondal, S. Regioselective Synthesis of Substituted Pyrrolopyridines Based on Pd(II)-Mediated Cross Coupling and Base Induced Heteroannulation Tetrahedron Lett. 2007, 48, 6951
    • (2007) Tetrahedron Lett. , vol.48 , pp. 6951
    • Majumdar, K.C.1    Mondal, S.2
  • 33
    • 79951676579 scopus 로고    scopus 로고
    • One-Pot Synthesis of 2-Bromo-4,5-diazafluoren-9-one via a Tandem Oxidationebromination-Rearrangement of Phenanthroline and its Hammer-Shaped Donoreacceptor Organic Semiconductors
    • Zhao, J.-F.; Chen, L.; Sun, P.-J.; Hou, X.-Y.; Zhao, X.-H.; Li, W.-J.; Xie, L.-H.; Qian, Y.; Shi, N.-E.; Lai, W.-Y.; Fan, Q.-L.; Huang, W. One-Pot Synthesis of 2-Bromo-4,5-diazafluoren-9-one via a Tandem Oxidationebromination- Rearrangement of Phenanthroline and its Hammer-Shaped Donoreacceptor Organic Semiconductors Tetrahedron 2011, 67, 1977
    • (2011) Tetrahedron , vol.67 , pp. 1977
    • Zhao, J.-F.1    Chen, L.2    Sun, P.-J.3    Hou, X.-Y.4    Zhao, X.-H.5    Li, W.-J.6    Xie, L.-H.7    Qian, Y.8    Shi, N.-E.9    Lai, W.-Y.10    Fan, Q.-L.11    Huang, W.12
  • 36
    • 77957140982 scopus 로고    scopus 로고
    • One-Pot Desulfurative-Fluorination-Bromination. Synthesis of 2,5-Dibromo-3-(1,1-difluoroalkyl)thiophenes
    • Turkman, N.; An, L.; Pomerantz, M. One-Pot Desulfurative-Fluorination- Bromination. Synthesis of 2,5-Dibromo-3-(1,1-difluoroalkyl)thiophenes Org. Lett. 2010, 12, 4428
    • (2010) Org. Lett. , vol.12 , pp. 4428
    • Turkman, N.1    An, L.2    Pomerantz, M.3
  • 38
    • 77954561662 scopus 로고    scopus 로고
    • Room Temperature, Copper-Catalyzed Amination of Bromonaphthyridines with Aqueous Ammonia
    • Anderson, A.; Taylor, P. G.; Zeller, M. A.; Zimmerman, S. C. Room Temperature, Copper-Catalyzed Amination of Bromonaphthyridines with Aqueous Ammonia J. Org. Chem. 2010, 75, 4848
    • (2010) J. Org. Chem. , vol.75 , pp. 4848
    • Anderson, A.1    Taylor, P.G.2    Zeller, M.A.3    Zimmerman, S.C.4
  • 39
    • 76049096060 scopus 로고    scopus 로고
    • Making Full Use of the Oxidizing Equivalents in Bromate in the Selective Oxidation of Thiols, Sulfides, and Benzylic/Secondary Alcohols into Disulfides, Sulfoxides, and Aldehydes/Ketones
    • Joshi, G.; Bhadra, S.; Ghosh, S.; Agrawal, M. K.; Ganguly, B.; Adimurthy, S.; Ghosh, P. K.; Ranu, B. C. Making Full Use of the Oxidizing Equivalents in Bromate in the Selective Oxidation of Thiols, Sulfides, and Benzylic/Secondary Alcohols into Disulfides, Sulfoxides, and Aldehydes/Ketones Ind. Eng. Chem. Res. 2010, 49, 1236
    • (2010) Ind. Eng. Chem. Res. , vol.49 , pp. 1236
    • Joshi, G.1    Bhadra, S.2    Ghosh, S.3    Agrawal, M.K.4    Ganguly, B.5    Adimurthy, S.6    Ghosh, P.K.7    Ranu, B.C.8
  • 40
    • 63849103125 scopus 로고    scopus 로고
    • Facile One-Pot Synthesis of α-Bromoketones from Olefins using Bromide/Bromate Couple as a Nonhazardous Brominating Agent
    • Patil, R. D.; Joshi, G.; Adimurthy, S.; Ranu, B. C. Facile One-Pot Synthesis of α-Bromoketones from Olefins using Bromide/Bromate Couple as a Nonhazardous Brominating Agent Tetrahedron Lett. 2009, 50, 2529
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2529
    • Patil, R.D.1    Joshi, G.2    Adimurthy, S.3    Ranu, B.C.4
  • 42
    • 38849101797 scopus 로고    scopus 로고
    • An Alternative Method for the Regio- and Stereoselective Bromination of Alkenes, Alkynes, Toluene Derivatives and Ketones using a Bromide/Bromate Couple
    • Adimurthy, S.; Ghosh, S.; Patoliya, P. U.; Ramachandraiah, G.; Agrawal, M.; Gandhi, M. R.; Upadhyay, S. C.; Ghosh, P. K.; Ranu, B. C. An Alternative Method for the Regio- and Stereoselective Bromination of Alkenes, Alkynes, Toluene Derivatives and Ketones using a Bromide/Bromate Couple Green Chem. 2008, 10, 232
    • (2008) Green Chem. , vol.10 , pp. 232
    • Adimurthy, S.1    Ghosh, S.2    Patoliya, P.U.3    Ramachandraiah, G.4    Agrawal, M.5    Gandhi, M.R.6    Upadhyay, S.C.7    Ghosh, P.K.8    Ranu, B.C.9
  • 43
    • 60949107951 scopus 로고    scopus 로고
    • Comparative Study of the Vicinal Functionalization of Olefins with 2:1 Bromide/Bromate and Iodide/Iodate Reagents
    • Agrawal, M. K.; Adimurthy, S.; Ganguly, B.; Ghosh, P. K. Comparative Study of the Vicinal Functionalization of Olefins with 2:1 Bromide/Bromate and Iodide/Iodate Reagents Tetrahedron 2009, 65, 2791
    • (2009) Tetrahedron , vol.65 , pp. 2791
    • Agrawal, M.K.1    Adimurthy, S.2    Ganguly, B.3    Ghosh, P.K.4
  • 44
    • 77956089043 scopus 로고    scopus 로고
    • 2: A Facile protocol for regioselective synthesis of bromohydrin, α-bromoketones and oxidation of benzylic/secondary alcohols to carbonyl compounds under mild aqueous conditions
    • 2: A Facile protocol for regioselective synthesis of bromohydrin, α-bromoketones and oxidation of benzylic/secondary alcohols to carbonyl compounds under mild aqueous conditions Ind. Eng. Chem. Res. 2010, 49, 8100
    • (2010) Ind. Eng. Chem. Res. , vol.49 , pp. 8100
    • Patil, R.D.1    Joshi, G.2    Adimurthy, S.3
  • 48
    • 80055042853 scopus 로고
    • Synthesis of Substituted Furans
    • Wright, G. F.; Gilman, H. Synthesis of Substituted Furans Ind. Eng. Chem. 1948, 40, 1517
    • (1948) Ind. Eng. Chem. , vol.40 , pp. 1517
    • Wright, G.F.1    Gilman, H.2
  • 49
    • 80055063874 scopus 로고    scopus 로고
    • John Wiley & Sons: New York
    • Brown, D. J. The Naphthyridines; John Wiley & Sons: New York, 2007; p 210.
    • (2007) The Naphthyridines , pp. 210
    • Brown, D.J.1
  • 50
    • 0010676687 scopus 로고    scopus 로고
    • New Age International (P), Ltd. New Delhi
    • Bansal, R. K. Heterocyclic Chemistry; New Age International (P), Ltd.: New Delhi, 2003; p 425.
    • (2003) Heterocyclic Chemistry , pp. 425
    • Bansal, R.K.1
  • 51
    • 0009340618 scopus 로고
    • Acid-Catalyzed Alpha-Halogenation of Amidines by Tetrahalomethanes. Kinetic- and Isotope-effect Evidence for the Intermediacy of the Ketene Aminal Tautomer
    • Lofas, S.; Ahlberg, P. Acid-Catalyzed Alpha-Halogenation of Amidines by Tetrahalomethanes. Kinetic- and Isotope-effect Evidence for the Intermediacy of the Ketene Aminal Tautomer J. Am. Chem. Soc. 1985, 107, 7534
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 7534
    • Lofas, S.1    Ahlberg, P.2
  • 53
    • 0033230747 scopus 로고    scopus 로고
    • Palladium (0)-Catalyzed Coupling of 6-Bromo and 3-Iodo Derivatives of 7-Methyl-4-oxo-1,4-dihydro[1,8]naphthyridines
    • Plisson, C.; Chenault, J. Palladium (0)-Catalyzed Coupling of 6-Bromo and 3-Iodo Derivatives of 7-Methyl-4-oxo-1,4-dihydro[1,8]naphthyridines Heterocycles 1999, 51, 2627
    • (1999) Heterocycles , vol.51 , pp. 2627
    • Plisson, C.1    Chenault, J.2
  • 54
    • 0018859019 scopus 로고
    • Synthesis of Antimicrobial Agents. IV. Synthesis and Antimicrobial Activities of Imidazo [4,5-b]-[1,8]-naphthyridine Derivatives
    • Suzuki, N.; Tanaka, Y.; Dohmori, R. Synthesis of Antimicrobial Agents. IV. Synthesis and Antimicrobial Activities of Imidazo [4,5-b]-[1,8]- naphthyridine Derivatives Chem. Pharm. Bull. 1980, 28, 235
    • (1980) Chem. Pharm. Bull. , vol.28 , pp. 235
    • Suzuki, N.1    Tanaka, Y.2    Dohmori, R.3
  • 55
    • 3242671823 scopus 로고    scopus 로고
    • A New Synthesis of Naphthyridinones and Quinolinones: Palladium-Catalyzed Amidation of o -Carbonyl-Substituted Aryl Halides
    • Manley, P. J.; Bilodeau, M. T. A New Synthesis of Naphthyridinones and Quinolinones: Palladium-Catalyzed Amidation of o -Carbonyl-Substituted Aryl Halides Org. Lett. 2004, 6, 2433
    • (2004) Org. Lett. , vol.6 , pp. 2433
    • Manley, P.J.1    Bilodeau, M.T.2
  • 56
    • 0025801032 scopus 로고
    • An Efficient Syntesis of 1,8-Naphthyridin-2(1H)-ones: Synthesis of Leukotriene Inhibitor SCH 37224
    • Nyce, P. L.; Gala, D.; Steinman, M. An Efficient Syntesis of 1,8-Naphthyridin-2(1H)-ones: Synthesis of Leukotriene Inhibitor SCH 37224 Synthesis 1991, 571
    • (1991) Synthesis , pp. 571
    • Nyce, P.L.1    Gala, D.2    Steinman, M.3
  • 57
    • 0037967993 scopus 로고    scopus 로고
    • A Convenient Synthesis of 4-aryl-1,8-naphthyridin-2(1 H)-ones by the Suzuki Coupling
    • Ban, H.; Muraoka, M.; Ohashi, N. A Convenient Synthesis of 4-aryl-1,8-naphthyridin-2(1 H)-ones by the Suzuki Coupling Tetrahedron Lett. 2003, 44, 6021
    • (2003) Tetrahedron Lett. , vol.44 , pp. 6021
    • Ban, H.1    Muraoka, M.2    Ohashi, N.3


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