메뉴 건너뛰기




Volumn 16, Issue 7, 2011, Pages 5963-5974

Synthetic organic electrochemistry in ionic liquids: The viscosity question

Author keywords

Carbamate oxidation; Constant current; Organic electrosynthesis; Room temperature ionic liquid; Viscosity

Indexed keywords

IONIC LIQUID;

EID: 79960813467     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16075963     Document Type: Article
Times cited : (17)

References (47)
  • 1
    • 57249093659 scopus 로고    scopus 로고
    • A short history of ionic liquids-From molten salts to neoteric solvents
    • Wilkes, J.S. A short history of ionic liquids-From molten salts to neoteric solvents. Green Chem. 2002, 10, 73-80.
    • (2002) Green Chem , vol.10 , pp. 73-80
    • Wilkes, J.S.1
  • 2
    • 79955884563 scopus 로고    scopus 로고
    • Room-temperature ionic liquids: Solvents for synthesis and catalysis
    • Hallett, J.P.; Welton, T. Room-temperature ionic liquids: Solvents for synthesis and catalysis. Chem. Rev. 2011, 111, 3508-3576.
    • (2011) Chem. Rev , vol.111 , pp. 3508-3576
    • Hallett, J.P.1    Welton, T.2
  • 4
    • 21344448826 scopus 로고    scopus 로고
    • Room temperature ionic liquids: Different classes and physical properties
    • DOI 10.2174/1385272054368411
    • Handy, S.T. Room temperature ionic liquids: Different classes and physical properties. Curr. Org. Chem. 2005, 9, 959-988. (Pubitemid 40903857)
    • (2005) Current Organic Chemistry , vol.9 , Issue.10 , pp. 959-988
    • Handy, S.T.1
  • 5
    • 0000034575 scopus 로고    scopus 로고
    • Ionic liquids-New "solutions" for transition metal catalysis
    • Wasserscheid, P.; Keim, W. Ionic liquids-New "solutions" for transition metal catalysis. Angew. Chem. Int. Ed. 2000, 39, 3772-3789.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 3772-3789
    • Wasserscheid, P.1    Keim, W.2
  • 7
    • 68949219465 scopus 로고    scopus 로고
    • A facile route to C2-substituted imidazolium ionic liquids
    • Ennis, E.; Handy, S.T. A facile route to C2-substituted imidazolium ionic liquids. Molecules 2009, 14, 2235-2245.
    • (2009) Molecules , vol.14 , pp. 2235-2245
    • Ennis, E.1    Handy, S.T.2
  • 8
    • 33751283202 scopus 로고    scopus 로고
    • One-pot halogenation-Heck coupling reactions in ionic liquids
    • DOI 10.1055/s-2006-948192
    • Handy, S.T. One-pot halogenation-Heck coupling reactions in ionic liquids. Synlett 2006, 3176-3178. (Pubitemid 44800030)
    • (2006) Synlett , Issue.18 , pp. 3176-3178
    • Handy, S.T.1
  • 9
    • 14544296566 scopus 로고    scopus 로고
    • The 2-position of imidazolium ionic liquids: Substitution and exchange
    • DOI 10.1021/jo0480850
    • Handy, S.T.; Okello, M. The 2-position of imidazolium ionic liquids: Substitution and exchange. . Org. Chem. 2005, 70, 1915-1918. (Pubitemid 40300160)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.5 , pp. 1915-1918
    • Handy, S.T.1    Okello, M.2
  • 10
    • 0141991233 scopus 로고    scopus 로고
    • Fructose-derived ionic liquids: Recyclable homogeneous supports
    • DOI 10.1016/j.tetlet.2003.09.121
    • Handy, S.T.; Okello, M. Fructose-derived ionic liquids: Recyclable homogeneous supports. Tetrahedron Lett. 2003, 44, 8399-8402. (Pubitemid 37249398)
    • (2003) Tetrahedron Letters , vol.44 , Issue.46 , pp. 8399-8402
    • Handy, S.T.1    Okello, M.2
  • 11
    • 0041806775 scopus 로고    scopus 로고
    • Greener solvents: Room temperature ionic liquids from biorenewable sources
    • Handy, S.T. Greener solvents: Room temperature ionic liquids from biorenewable sources. Chem. Eur. J. 2003, 9, 2938-2944.
    • (2003) Chem. Eur. J , vol.9 , pp. 2938-2944
    • Handy, S.T.1
  • 12
    • 0141742644 scopus 로고    scopus 로고
    • Solvents from biorenewable sources: Ionic liquids based on fructose
    • DOI 10.1021/ol034778b
    • Handy, S.T.; Okello, M.; Dickenson, G. Solvents from biorenewable sources: Ionic liquids based on fructose. Org. Lett. 2003, 5, 2513-2515. (Pubitemid 37140897)
    • (2003) Organic Letters , vol.5 , Issue.14 , pp. 2513-2515
    • Handy, S.T.1    Okello, M.2    Dickenson, G.3
  • 14
    • 49049111875 scopus 로고    scopus 로고
    • Electrochemical reactivity in room-temperature ionic liquids
    • Hapiot, P.; Lagrost, C. Electrochemical reactivity in room-temperature ionic liquids. Chem. Rev. 2008, 108, 2238-2264.
    • (2008) Chem. Rev , vol.108 , pp. 2238-2264
    • Hapiot, P.1    Lagrost, C.2
  • 15
    • 1842536074 scopus 로고    scopus 로고
    • Superoxide-stable ionic liquids: New and efficient media for electrosynthesis of functional siloxanes
    • Martiz, B.; Keyrouz, R.; Gmouh, S.; Vaultier, M.; Jouikov, V. Superoxide-stable ionic liquids: New and efficient media for electrosynthesis of functional siloxanes. Chem. Commun. 2004, 674-675. (Pubitemid 38445227)
    • (2004) Chemical Communications , Issue.6 , pp. 674-675
    • Martiz, B.1    Keyrouz, R.2    Gmouh, S.3    Vaultier, M.4    Jouikov, V.5
  • 16
    • 3142575279 scopus 로고    scopus 로고
    • Electrochemical synthesis and in situ spectoelectrochemical characterization of poly(3,4-ethylenedioxythhiophene) (PEDOT) in room temperature ionic liquids
    • Damlin, P.; Kvarnström, C.; Ivaska, A. Electrochemical synthesis and in situ spectoelectrochemical characterization of poly(3,4- ethylenedioxythhiophene) (PEDOT) in room temperature ionic liquids. J. Electroanal. Chem. 2004, 570, 113-122.
    • (2004) J. Electroanal. Chem , vol.570 , pp. 113-122
    • Damlin, P.1    Kvarnström, C.2    Ivaska, A.3
  • 17
    • 0142031473 scopus 로고    scopus 로고
    • Electrooxidative polymerization of aromatic compounds in 1-ethyl-3-methylimidazolium trifluoromethanesulfonate room-temperature ionic liquid
    • Sekiguchi, K.; Atobe, M.; Fuchigami, T. Electrooxidative polymerization of aromatic compounds in 1-ethyl-3-methylimidazolium trifluoromethanesulfonate room-temperature ionic liquid. J. Electroanal. Chem. 2003, 557, 1-7.
    • (2003) J. Electroanal. Chem , vol.557 , pp. 1-7
    • Sekiguchi, K.1    Atobe, M.2    Fuchigami, T.3
  • 18
    • 3242727965 scopus 로고    scopus 로고
    • Electroorganic synthesis using a fluoride ion mediator under ultrasonic irradiation: Synthesis of oxindole and 3-oxotetrahydroisoquinoline derivatives
    • DOI 10.1021/ol049152f
    • Shen, Y.; Atobe, M.; Fuchigami, T. Electroorganic synthesis using a fluoride ion mediator under ultrasonic irradiation: Synthesis of oxindole and 3-oxotetrahydroisoquinoline derivatives. Org. Lett. 2004, 6, 2441-2444. (Pubitemid 38952558)
    • (2004) Organic Letters , vol.6 , Issue.14 , pp. 2441-2444
    • Shen, Y.1    Atobe, M.2    Fuchigami, T.3
  • 19
    • 56749153715 scopus 로고    scopus 로고
    • Anodic fluorination and fluorodesulfurization in ionic liquid hydrogen fluoride salts with polyether additives
    • Sawamura, T.; Inagi, S.; Fuchigami, T. Anodic fluorination and fluorodesulfurization in ionic liquid hydrogen fluoride salts with polyether additives. J. Electrochem. Soc. 2009, E26-E28.
    • (2009) J. Electrochem. Soc
    • Sawamura, T.1    Inagi, S.2    Fuchigami, T.3
  • 20
    • 33748430355 scopus 로고    scopus 로고
    • Regioselective anodic monofluorination of ethers, lactones, carbonates, and esters using ionic liquid fluoride salts
    • DOI 10.1149/1.2222891
    • Hasegawa, M.; Ishii, H.; Cao, Y.; Fuchigami, T. Regioselective anodic monofluorination of ethers, lactones, carbonates, and esters using ionic liquid fluoride salts. J. Electrochem. Soc. 2006, D162-D166. (Pubitemid 44343854)
    • (2006) Journal of the Electrochemical Society , vol.153 , Issue.10
    • Hasegawa, M.1    Ishii, H.2    Cao, Y.3    Fuchigami, T.4
  • 21
    • 0345724785 scopus 로고    scopus 로고
    • Selective anodic fluorination of phthalides in ionic liquids
    • DOI 10.1039/b304617f
    • Hasegawa, M.; Ishii, H.; Fuchigami, T. Selective anodic fluorination of phthalides in ionic liquids. Green Chem. 2003, 5, 512-515. (Pubitemid 37443708)
    • (2003) Green Chemistry , vol.5 , Issue.5 , pp. 512-515
    • Hasegawa, M.1    Ishii, H.2    Fuchigami, T.3
  • 22
    • 0037127565 scopus 로고    scopus 로고
    • Electroorganic synthesis under solvent-free conditions. Highly regioselective anodic monofluorination of cyclic ethers, lactones, and a cyclic carbonate
    • Hasegawa, M. Ishii, H. Fuchigami, T. Electroorganic synthesis under solvent-free conditions. Highly regioselective anodic monofluorination of cyclic ethers, lactones, and a cyclic carbonate. Tetrahedron Lett. 2002, 43, 1503-1505.
    • (2002) Tetrahedron Lett , vol.43 , pp. 1503-1505
    • Ishii, H.M.1    Fuchigami, T.H.2
  • 23
    • 2642559696 scopus 로고    scopus 로고
    • Electroorganic reactions in ionic liquids 5 {1}. Anodic fluorodesulfurization of phthalide, ethylene carbonate, and glucopyranosides having arylthio groups
    • Hasegawa, M.; Fuchigami, T. Electroorganic reactions in ionic liquids 5 {1}. Anodic fluorodesulfurization of phthalide, ethylene carbonate, and glucopyranosides having arylthio groups. Electrochim. Acta 2004, 49, 3367-3372.
    • (2004) Electrochim. Acta , vol.49 , pp. 3367-3372
    • Hasegawa, M.1    Fuchigami, T.2
  • 25
    • 40149084621 scopus 로고    scopus 로고
    • 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO)-mediated catalytic oxidation of benzyl alcohol in acetonitrile and ionic liquid 1-buthyl-3-methyl- imidazolium hexafluorophosphate [BMIM][PF6]: Kinetic analysis
    • Herath, A.C.; Becker, J.Y. 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO)-mediated catalytic oxidation of benzyl alcohol in acetonitrile and ionic liquid 1-buthyl-3-methyl-imidazolium hexafluorophosphate [BMIM][PF6]: Kinetic analysis. Electrochim. Acta 2008, 53, 4324-4330.
    • (2008) Electrochim. Acta , vol.53 , pp. 4324-4330
    • Herath, A.C.1    Becker, J.Y.2
  • 26
    • 33744826327 scopus 로고    scopus 로고
    • Indirect catalytic epoxidation with hydrogen peroxide electrogenerated in ionic liquids
    • DOI 10.1016/j.tet.2005.12.075, PII S0040402006007034
    • Ho, K.-P.; Wong, K.-Y.; Chan, T.H. Indirect catalytic epoxidation with hydrogen peroxide electrogenerated in ionic liquids. Tetrahedron 2006, 62, 6650-6658. (Pubitemid 43831943)
    • (2006) Tetrahedron , vol.62 , Issue.28 , pp. 6650-6658
    • Ho, K.-P.1    Wong, K.-Y.2    Chan, T.H.3
  • 27
    • 16244393120 scopus 로고    scopus 로고
    • Electrosynthesis of hydrogen peroxide in room temperature ionic liquids and in situ epoxidation of alkenes
    • DOI 10.1039/b416837b
    • Tang, M.C.-Y.; Wong, K.-Y.; Chan, T.H. Electrosynthesis of hydrogen peroxide in room temperature ionic liquids and in situ epoxidation of alkenes. Chem. Commun. 2005, 1345-1347. (Pubitemid 40459995)
    • (2005) Chemical Communications , Issue.10 , pp. 1345-1347
    • Tang, M.C.-Y.1    Wong, K.-Y.2    Chan, T.H.3
  • 28
    • 0035928707 scopus 로고    scopus 로고
    • First example of electroassisted biomimetic activation of molecular oxygen by a (salen)Mn epoxidation catalyst in a room-temperature ionic liquid
    • Gaillon, L.; Bedioui, F. First example of electroassisted biomimetic activation of molecular oxygen by a (salen)Mn epoxidation catalyst in a room-temperature ionic liquid. Chem. Commun. 2001, 1458-1459. (Pubitemid 32747798)
    • (2001) Chemical Communications , Issue.16 , pp. 1458-1459
    • Gaillon, L.1    Bedioui, F.2
  • 29
    • 21144453578 scopus 로고    scopus 로고
    • The influence of room-temperature ionic liquids on the stereoselectivity and kinetics of the electrochemical pinacol coupling of acetophenone
    • DOI 10.1039/b500839e
    • Lagrost, C.; Hapiot, P.; Vaultier, M. The influence of room-temperature ionic liquids on the stereoselectivity and kinetics of the electrochemical pinacol coupling of acetophenone. Green Chem. 2005, 7, 468-474. (Pubitemid 40879630)
    • (2005) Green Chemistry , vol.7 , Issue.6 , pp. 468-474
    • Lagrost, C.1    Hapiot, P.2    Vaultier, M.3
  • 30
    • 17444426646 scopus 로고    scopus 로고
    • Electroreduction of N-methylphthalimide in room temperature ionic liquids under insonated and silent conditions
    • DOI 10.1016/j.ultsonch.2004.08.001
    • Villagrán, C.; Banks, C.; Pitner, W.; Hardacre, C.; Compton, R.G. Electroreduction of N-methylphthalimide in room temperature ionic liquids under insonated and silent conditions. Ultrasonics Sonochemistry 2005, 12, 423-428. (Pubitemid 40545975)
    • (2005) Ultrasonics Sonochemistry , vol.12 , Issue.6 , pp. 423-428
    • Villagran, C.1    Banks, C.E.2    Pitner, W.R.3    Hardacre, C.4    Compton, R.G.5
  • 31
    • 23844476894 scopus 로고    scopus 로고
    • Oxidative self-coupling of aromatic compounds in ionic liquids
    • DOI 10.1016/j.elecom.2005.06.002, PII S1388248105001657
    • Mellah, M.; Zeitouny, J.; Gmouh, S.; Vaultier, M.; Jouikov, V. Oxidative self-coupling of aromatic compounds in ionic liquids. Electrochem. Commun. 2005, 7, 869-874. (Pubitemid 41164072)
    • (2005) Electrochemistry Communications , vol.7 , Issue.9 , pp. 869-874
    • Mellah, M.1    Zeitouny, J.2    Gmouh, S.3    Vaultier, M.4    Jouikov, V.5
  • 34
    • 0038040625 scopus 로고    scopus 로고
    • Room-temperature ionic liquids as new solvents for organic electrosynthesis. The first examples of direct or nickel-catalysed electroreductive coupling involving organic halides
    • Barhdadi, R.; Courtinard, C.; Nédélee, J.Y.; Troupel, M. Room-temperature ionic liquids as new solvents for organic electrosynthesis. The first examples of direct or nickel-catalysed electroreductive coupling involving organic halides. Chem. Commun. 2003, 1434-1435. (Pubitemid 36734965)
    • (2003) Chemical Communications , Issue.12 , pp. 1434-1435
    • Barhdadi, R.1    Courtinard, C.2    Nedelec, J.Y.3    Troupel, M.4
  • 35
    • 34249297954 scopus 로고    scopus 로고
    • 12 towards the dechlorination of DDT in ionic liquid
    • DOI 10.1039/b700725f
    • Jabbar, M.A.; Shimakoshi, H.; Hisaeda, Y. Enhanced reactivity of hydrophobic vitamin B12 towards the dechlorination of DDT in ionic liquid. Chem. Commun. 2007, 1653-1655. (Pubitemid 46813950)
    • (2007) Chemical Communications , Issue.16 , pp. 1653-1655
    • Jabbar, Md.A.1    Shimakoshi, H.2    Hisaeda, Y.3
  • 36
    • 50249101313 scopus 로고    scopus 로고
    • Reactivity of electrogenerated N-heterocyclic carbenes in room-temperature ionic liquids. Cyclization to 2-azetidinone ring via C-3/C-4 bond formation
    • Feroci, M.; Chiarotto, I.; Orsini, M.; Sotgiu, G.; Inesi, A. Reactivity of electrogenerated N-heterocyclic carbenes in room-temperature ionic liquids. Cyclization to 2-azetidinone ring via C-3/C-4 bond formation. Adv. Synth. Catal. 2008, 350, 1355-1359.
    • (2008) Adv. Synth. Catal , vol.350 , pp. 1355-1359
    • Feroci, M.1    Chiarotto, I.2    Orsini, M.3    Sotgiu, G.4    Inesi, A.5
  • 37
    • 0037034082 scopus 로고    scopus 로고
    • Electrochemical activation of carbon dioxide in ionic liquid: Synthesis of cyclic carbonates at mild reaction conditions
    • Yang, H.; Gu, Y.; Deng, Y.; Shi, F. Electrochemical activation of carbon dioxide in ionic liquid: synthesis of cyclic carbonates at mild reaction conditions. Chem. Commun. 2002, 274-275. (Pubitemid 34146485)
    • (2002) Chemical Communications , Issue.3 , pp. 274-275
    • Yang, H.1    Gu, Y.2    Deng, Y.3    Shi, F.4
  • 38
    • 38849189455 scopus 로고    scopus 로고
    • 4): Synthesis of organic carbonates under mild conditions
    • DOI 10.1039/b711981j
    • 4): Synthesis of organic carbonates under mild conditions. Green Chem. 2008, 10, 202-206. (Pubitemid 351199054)
    • (2008) Green Chemistry , vol.10 , Issue.2 , pp. 202-206
    • Zhang, L.1    Niu, D.2    Zhang, K.3    Zhang, G.4    Luo, Y.5    Lu, J.6
  • 39
    • 57849153303 scopus 로고    scopus 로고
    • Electrogenerated N-heterocyclic carbene: N-Acylation of chiral oxaolidin-2-ones in ionic liquids
    • Chiarotto, I.; Feeney, M.M.M.; Feroci, M.; Inesi, A. Electrogenerated N-heterocyclic carbene: N-Acylation of chiral oxaolidin-2-ones in ionic liquids. Electrochim. Acta 2009, 54, 1638-1644.
    • (2009) Electrochim. Acta , vol.54 , pp. 1638-1644
    • Chiarotto, I.1    Feeney, M.M.M.2    Feroci, M.3    Inesi, A.4
  • 40
    • 78650403986 scopus 로고    scopus 로고
    • Study on the reactivity of aldehydes in electrolyzed ionic liquids: Benzoin condensation-volatile organic compounds (VOCs) vs. Room temperature ionic liquids (RTILs)
    • Chiarotto, I.; Feroci, M.; Feeney, M.M.M.; Inesi, A. Study on the reactivity of aldehydes in electrolyzed ionic liquids: Benzoin Condensation-Volatile Organic Compounds (VOCs) vs. Room Temperature Ionic Liquids (RTILs). Adv. Synth. Catal. 2010, 352, 3287-3292.
    • (2010) Adv. Synth. Catal , vol.352 , pp. 3287-3292
    • Chiarotto, I.1    Feroci, M.2    Feeney, M.M.M.3    Inesi, A.4
  • 41
    • 0001191368 scopus 로고
    • Facile and efficient carboalkoxylation and carboaryloxylation of amines
    • Kita, Y.; Haruta, J.; Tagawa, H.; Tamura, Y. Facile and efficient carboalkoxylation and carboaryloxylation of amines. J. Org. Chem. 1980, 45, 4519-4522.
    • (1980) J. Org. Chem , vol.45 , pp. 4519-4522
    • Kita, Y.1    Haruta, J.2    Tagawa, H.3    Tamura, Y.4
  • 42
    • 0034583236 scopus 로고    scopus 로고
    • Influence of chloride, water, and organic solvents on the physical properties of ionic liquids
    • Seddon, K.R.; Stark, A.; Torres, M.-J. Influence of chloride, water, and organic solvents on the physical properties of ionic liquids. Pure Appl. Chem. 2000, 72, 2275-2287.
    • (2000) Pure Appl. Chem , vol.72 , pp. 2275-2287
    • Seddon, K.R.1    Stark, A.2    Torres, M.-J.3
  • 43
    • 34848895098 scopus 로고    scopus 로고
    • An acidity scale of 1,3-dialkylimidazolium salts in dimethyl sulfoxide solution
    • DOI 10.1021/jo070973i
    • Chu, Y.; Deng, H.; Cheng, J.-P. An Acidity Scale of 1,3- Dialkylimidazolium Salts in Dimethyl Sulfoxide Solution. J. Org. Chem. 2007, 72, 7790-7793. (Pubitemid 47501654)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.20 , pp. 7790-7793
    • Chu, Y.1    Deng, H.2    Cheng, J.-P.3
  • 44
    • 0042882233 scopus 로고    scopus 로고
    • TBD-catalyzed solventless synthesis of symmetrically N,N'-substituted ureas from primary amines and diethyl carbonate
    • Ballini, R.; Fiorini, D.; Maggi, R.; Righi, P.; Sartori, G.; Sartorio, R. TBD-catalyzed solventless synthesis of symmetrically N,N'-substituted ureas from primary amines and diethyl carbonate. Green Chem. 2003, 5, 396-398.
    • (2003) Green Chem , vol.5 , pp. 396-398
    • Ballini, R.1    Fiorini, D.2    Maggi, R.3    Righi, P.4    Sartori, G.5    Sartorio, R.6
  • 45
    • 0000860321 scopus 로고
    • Electroorganic chemistry. 46. A new carbon-carbon bond forming reaction at the -position of amines utilizing anodic oxidation as a key step
    • Shono, T.; Matsumura, Y.; Tsubata, K. Electroorganic chemistry. 46. A new carbon-carbon bond forming reaction at the -position of amines utilizing anodic oxidation as a key step. J. Am. Chem. Soc. 1981, 103, 1172-1176.
    • (1981) J. Am. Chem. Soc , vol.103 , pp. 1172-1176
    • Shono, T.1    Matsumura, Y.2    Tsubata, K.3
  • 46
    • 0001349480 scopus 로고
    • Facile access to 6-methoxy-1,2,3,6-tetrahydroand 4-hydroxy-1,2,3,4- tetrahydropyridines by electrochemical haloalkoxylation-dehydrohalogenation sequence as a key operation
    • Torii, S.; Inokuchi, T.; Akahosi, F.; Kubota, M. Facile access to 6-methoxy-1,2,3,6-tetrahydroand 4-hydroxy-1,2,3,4-tetrahydropyridines by electrochemical haloalkoxylation-dehydrohalogenation sequence as a key operation. Synthesis 1987, 3, 242-245.
    • (1987) Synthesis , vol.3 , pp. 242-245
    • Torii, S.1    Inokuchi, T.2    Akahosi, F.3    Kubota, M.4
  • 47
    • 0019997481 scopus 로고
    • Synthesis of 5-fluorouracil derivatives having N-acylazacycloakanes and lactams
    • DOI 10.1021/jo00348a020
    • Nishitani, T.; Horikawa, H.; Iwasaki, T.; Matsumoto, K.; Inoue, I.; Miyoshi, M. Synthetic electroorganic chemistry. 14. Synthesis of 5-fluorouracil derivatives having N-acylazacycloalkanes and lactams. J. Org. Chem. 1982, 47, 1706-1712. (Pubitemid 12094488)
    • (1982) Journal of Organic Chemistry , vol.47 , Issue.9 , pp. 1706-1712
    • Nishitani, T.1    Horikawa, H.2    Iwasaki, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.