메뉴 건너뛰기




Volumn 55, Issue 10, 2012, Pages 2009-2017

Ferric perchlorate-mediated radical reactions of [60]fullerene

Author keywords

keto esters; 60 fullerene; Aldehydes ketones; Arylboronic acids; Ferric perchlorate; Malonate esters; Nitriles

Indexed keywords

[60] FULLERENE; ARYLBORONIC ACIDS; FERRIC PERCHLORATE; KETO ESTER; MALONATES; NITRILES;

EID: 84869081553     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-012-4714-7     Document Type: Conference Paper
Times cited : (20)

References (70)
  • 1
    • 0027607561 scopus 로고
    • The chemistry of fullerenes
    • Taylor R, Walton DRM. The chemistry of fullerenes. Nature, 1993, 363: 685-693
    • (1993) Nature , vol.363 , pp. 685-693
    • Taylor, R.1    Walton, D.R.M.2
  • 2
    • 0029089510 scopus 로고
    • Addition reactions of buckminsterfullerene (C60)
    • Hirsch A. Addition reactions of buckminsterfullerene (C60). Synthesis, 1995, 895-913
    • (1995) Synthesis , pp. 895-913
    • Hirsch, A.1
  • 3
    • 84911358722 scopus 로고    scopus 로고
    • Cycloaddition to buckminsterfullerene C60: Advancements and future prospects
    • Yurovskaya MA, Trushkov IV. Cycloaddition to buckminsterfullerene C60: Advancements and future prospects. Russ Chem Bull Int Ed, 2002, 51: 367-443
    • (2002) Russ Chem Bull Int Ed , vol.51 , pp. 367-443
    • Yurovskaya, M.A.1    Trushkov, I.V.2
  • 4
    • 33846194601 scopus 로고    scopus 로고
    • Structural aspects of fullerene chemistry: A journey through fullerene chirality
    • Thilgen C, Diederich F. Structural aspects of fullerene chemistry: A journey through fullerene chirality. Chem Rev, 2006, 106: 5049-5135
    • (2006) Chem Rev , vol.106 , pp. 5049-5135
    • Thilgen, C.1    Diederich, F.2
  • 5
    • 51049104046 scopus 로고    scopus 로고
    • Selective multiaddition of organocopper reagents to fullerenes
    • Matsuo Y, Nakamura E. Selective multiaddition of organocopper reagents to fullerenes. Chem Rev, 2008, 108: 3016-3028
    • (2008) Chem Rev , vol.108 , pp. 3016-3028
    • Matsuo, Y.1    Nakamura, E.2
  • 6
    • 0001223050 scopus 로고    scopus 로고
    • Fullerene materials
    • Prato M. Fullerene materials. Top Curr Chem, 1999, 199: 173-187
    • (1999) Top Curr Chem , vol.199 , pp. 173-187
    • Prato, M.1
  • 7
    • 0040705304 scopus 로고    scopus 로고
    • Supramolecular fullerene chemistry
    • Diederich F, Gómez-López M. Supramolecular fullerene chemistry. Chem Soc Rev, 1999, 28: 263-277
    • (1999) Chem Soc Rev , vol.28 , pp. 263-277
    • Diederich, F.1    Gómez-López, M.2
  • 8
    • 0344393787 scopus 로고    scopus 로고
    • Functionalized fullerenes in water. The first 10 years of their chemistry, biology, and nanoscience
    • Nakamura E, Isobe H. Functionalized fullerenes in water.The first 10 years of their chemistry, biology, and nanoscience. Acc Chem Res, 2003, 36: 807-815
    • (2003) Acc Chem Res , vol.36 , pp. 807-815
    • Nakamura, E.1    Isobe, H.2
  • 10
    • 34250882701 scopus 로고    scopus 로고
    • Synthesis of [60]fullerene acetals and ketals: Reaction of [60]fullerene with aldehydes/ketones and alkoxides
    • Wang GW, Li FB, Chen ZX, Wu P, Cheng B, Xu Y. Synthesis of [60]fullerene acetals and ketals: Reaction of [60]fullerene with aldehydes/ketones and alkoxides. J Org Chem, 2007, 72: 4779-4783
    • (2007) J Org Chem , vol.72 , pp. 4779-4783
    • Wang, G.W.1    Li, F.B.2    Chen, Z.X.3    Wu, P.4    Cheng, B.5    Xu, Y.6
  • 11
    • 70349558255 scopus 로고    scopus 로고
    • An efficient approach to chiral fullerene derivatives by catalytic enantioselective 1, 3-dipolar cycloadditions
    • Filippone S, Maroto EE, Martín-Domenech Á, Suarez M, Martín N. An efficient approach to chiral fullerene derivatives by catalytic enantioselective 1, 3-dipolar cycloadditions. Nat Chem, 2009, 1: 578-582
    • (2009) Nat Chem , vol.1 , pp. 578-582
    • Filippone, S.1    Maroto, E.E.2    Martín-Domenech, Á.3    Suarez, M.4    Martín, N.5
  • 12
    • 64349102342 scopus 로고    scopus 로고
    • 1, 4-Fullerenols C60ArOH: Synthesis and functionalization
    • Wang GW, Lu YM, Chen ZX. 1, 4-Fullerenols C60ArOH: Synthesis and functionalization. Org Lett, 2009, 11: 1507-1510
    • (2009) Org Lett , vol.11 , pp. 1507-1510
    • Wang, G.W.1    Lu, Y.M.2    Chen, Z.X.3
  • 13
    • 67649612813 scopus 로고    scopus 로고
    • An alternative type of fullerene products from the reaction of [60]fullerene with alkoxides and subsequent derivatization
    • Wang GW, Lu YM, Chen ZX, Wu SH. An alternative type of fullerene products from the reaction of [60]fullerene with alkoxides and subsequent derivatization. J Org Chem, 2009, 74: 4841-4848
    • (2009) J Org Chem , vol.74 , pp. 4841-4848
    • Wang, G.W.1    Lu, Y.M.2    Chen, Z.X.3    Wu, S.H.4
  • 14
    • 77956254541 scopus 로고    scopus 로고
    • Copper-catalyzed formal [4+2] annulation between alkyne and fullerene bromide
    • Xiao Z, Matsuo Y, Nakamura E. Copper-catalyzed formal [4+2] annulation between alkyne and fullerene bromide. J Am Chem Soc, 2010, 132: 12234-12236
    • (2010) J Am Chem Soc , vol.132 , pp. 12234-12236
    • Xiao, Z.1    Matsuo, Y.2    Nakamura, E.3
  • 15
    • 79952275253 scopus 로고    scopus 로고
    • Aziridinofullerene: A versatile platform for functionalized fullerenes
    • Nambo M, Segawa Y, Itami K. Aziridinofullerene: A versatile platform for functionalized fullerenes. J Am Chem Soc, 2011, 133: 2402-2405
    • (2011) J Am Chem Soc , vol.133 , pp. 2402-2405
    • Nambo, M.1    Segawa, Y.2    Itami, K.3
  • 17
    • 80051597084 scopus 로고    scopus 로고
    • Cobalt-catalyzed hydroalkylation of [60]fullerene with active alkyl bromides: Selective synthesis of monoalkylated fullerenes
    • Lu S, Jin T, Bao M, Yamamoto Y. Cobalt-catalyzed hydroalkylation of [60]fullerene with active alkyl bromides: Selective synthesis of monoalkylated fullerenes. J Am Chem Soc, 2011, 133: 12842-12848
    • (2011) J Am Chem Soc , vol.133 , pp. 12842-12848
    • Lu, S.1    Jin, T.2    Bao, M.3    Yamamoto, Y.4
  • 18
    • 84855770696 scopus 로고    scopus 로고
    • Highly efficient Cu(OAc) 2-catalyzed dimerization of monofunctionalized hydrofullerenes leading to single-bonded [60]fullerene dimers
    • Lu S, Jin T, Kwon E, Bao M, Yamamoto Y. Highly efficient Cu(OAc)2-catalyzed dimerization of monofunctionalized hydrofullerenes leading to single-bonded [60]fullerene dimers. Angew Chem Int Ed, 2012, 51: 802-806
    • (2012) Angew Chem Int Ed , vol.51 , pp. 802-806
    • Lu, S.1    Jin, T.2    Kwon, E.3    Bao, M.4    Yamamoto, Y.5
  • 22
    • 34447530940 scopus 로고    scopus 로고
    • Radical reactions of [60]fullerene mediated by manganese(III) acetate dihydrate
    • For reviews, see: Wang GW, Li FB. Radical reactions of [60]fullerene mediated by manganese(III) acetate dihydrate. J Nanosci Nanotech, 2007, 7: 1162-1175;
    • (2007) J Nanosci Nanotech , pp. 1162-1167
    • Wang, G.W.1    Li, F.B.2
  • 23
    • 84862529539 scopus 로고    scopus 로고
    • Transition metal salt-mediated radical reactions of [60]fullerene
    • Wang GW, Li FB. Transition metal salt-mediated radical reactions of [60]fullerene. Curr Org Chem, 2012, 16: 1109-1127
    • (2012) Curr Org Chem , vol.16 , pp. 1109-1127
    • Wang, G.W.1    Li, F.B.2
  • 24
    • 0348167670 scopus 로고    scopus 로고
    • Reaction of [60]fullerene with free radicals generated from active methylene compounds by manganese (III) acetate dihydrate
    • Zhang TH, Lu P, Wang F, Wang GW. Reaction of [60]fullerene with free radicals generated from active methylene compounds by manganese (III) acetate dihydrate. Org Biomol Chem, 2003, 1: 4403-4407
    • (2003) Org Biomol Chem , vol.1 , pp. 4403-4407
    • Zhang, T.H.1    Lu, P.2    Wang, F.3    Wang, G.W.4
  • 25
    • 2342477172 scopus 로고    scopus 로고
    • Selective addition to [60]fullerene of two different radicals generated from Mn(III)-based radical reaction
    • Wang GW, Zhang TH, Cheng X, Wang F. Selective addition to [60]fullerene of two different radicals generated from Mn(III)-based radical reaction. Org Biomol Chem, 2004, 2: 1160-1163
    • (2004) Org Biomol Chem , Issue.2 , pp. 1160-1163
    • Wang, G.W.1    Zhang, T.H.2    Cheng, X.3    Wang, F.4
  • 26
    • 10644295760 scopus 로고    scopus 로고
    • Manganese(III) acetate-mediated free radical reactions of [60]fullerene with β-Dicarbonyl compounds
    • Li C, Zhang D, Zhang X, Wu S, Gao X. Manganese(III) acetate-mediated free radical reactions of [60]fullerene with β-dicarbonyl compounds. Org Biomol Chem, 2004, 2: 3464-3469
    • (2004) Org Biomol Chem , vol.2 , pp. 3464-3469
    • Li, C.1    Zhang, D.2    Zhang, X.3    Wu, S.4    Gao, X.5
  • 27
    • 12144249207 scopus 로고    scopus 로고
    • Manganese(III) acetate based radical cycloaddition of tertiary diallylamines with [60]fullerene
    • Zou YL, Zhang DW, Liu Y, Luo Z, Wu SH, Gao X. Manganese(III) acetate based radical cycloaddition of tertiary diallylamines with [60]fullerene. Chin J Org Chem, 2004, 24: 1614-1618
    • (2004) Chin J Org Chem , vol.24 , pp. 1614-1618
    • Zou, Y.L.1    Zhang, D.W.2    Liu, Y.3    Luo, Z.4    Wu, S.H.5    Gao, X.6
  • 28
    • 15244362031 scopus 로고    scopus 로고
    • Cu(II) acetate-And Mn(III) acetate-mediated radi cal reactions of [60]fullerene with ketonic compounds
    • Wang GW, Li FB. Cu(II) acetate-and Mn(III) acetate-mediated radi cal reactions of [60]fullerene with ketonic compounds. Org Biomol Chem, 2005, 3: 794-797
    • (2005) Org Biomol Chem , vol.3 , pp. 794-797
    • Wang, G.W.1    Li, F.B.2
  • 29
    • 33745031248 scopus 로고    scopus 로고
    • Solvent-free synthesis of dihydrofuran-fused [60]fullerene derivatives by high-speed vibration milling
    • Cheng X, Wang GW, Murata Y, Komatsu K. Solvent-free synthesis of dihydrofuran-fused [60]fullerene derivatives by high-speed vibration milling. Chin Chem Lett, 2005, 16: 1327-1329
    • (2005) Chin Chem Lett , vol.16 , pp. 1327-1329
    • Cheng, X.1    Wang, G.W.2    Murata, Y.3    Komatsu, K.4
  • 30
    • 33745471433 scopus 로고    scopus 로고
    • Radical reactions of [60]fullerene with β-enamino carbonyl compounds mediated by manganese(III) acetate
    • Wang GW, Yang HT, Miao CB, Xu Y. Radical reactions of [60]fullerene with β-enamino carbonyl compounds mediated by manganese(III) acetate. Org Biomol Chem, 2006, 4: 2595-2599
    • (2006) Org Biomol Chem , vol.4 , pp. 2595-2599
    • Wang, G.W.1    Yang, H.T.2    Miao, C.B.3    Xu, Y.4
  • 31
    • 33645940925 scopus 로고    scopus 로고
    • [60]Fullerene-fused lactones: Manganese (III) acetate-mediated synthesis and novel reductive ring opening
    • Wang GW, Li FB, Zhang TH. [60]Fullerene-fused lactones: Manganese (III) acetate-mediated synthesis and novel reductive ring opening. Org Lett, 2006, 8: 1355-1358
    • (2006) Org Lett , vol.8 , pp. 1355-1358
    • Wang, G.W.1    Li, F.B.2    Zhang, T.H.3
  • 32
    • 70349861772 scopus 로고    scopus 로고
    • Synthesis of fullerene-fused lactones and fullerenyl esters: Radical reaction of [60]fullerene with carboxylic acids promoted by manganese(III) acetate and lead(IV) acetate
    • Li FB, Liu TX, Huang YS, Wang GW. Synthesis of fullerene-fused lactones and fullerenyl esters: Radical reaction of [60]fullerene with carboxylic acids promoted by manganese(III) acetate and lead(IV) acetate. J Org Chem, 2009, 74: 7743-7749
    • (2009) J Org Chem , vol.74 , pp. 7743-7749
    • Li, F.B.1    Liu, T.X.2    Huang, Y.S.3    Wang, G.W.4
  • 33
    • 77956515298 scopus 로고    scopus 로고
    • Manganese(III) acetate-mediated radical reaction of [60]fullerene with bromoacetic acid, 3-chloropropionic acid or 1-naphthylacetic acid
    • Li FB, Zhu SE, Wang GW. Manganese(III) acetate-mediated radical reaction of [60]fullerene with bromoacetic acid, 3-chloropropionic acid or 1-naphthylacetic acid. Chin Sci Bull, 2010, 55: 2909-2914
    • (2010) Chin Sci Bull , vol.55 , pp. 2909-2914
    • Li, F.B.1    Zhu, S.E.2    Wang, G.W.3
  • 34
    • 79956063178 scopus 로고    scopus 로고
    • Manganese(III) acetatemediated radical reaction of [60]fullerene with phosphonate esters affording unprecedented separable singly-bonded [60]fullerene dimmers
    • Wang GW, Wang CZ, Zhu SE, Murata Y. Manganese(III) acetatemediated radical reaction of [60]fullerene with phosphonate esters affording unprecedented separable singly-bonded [60]fullerene dimmers. Chem Commun, 2011, 47: 6111-6113
    • (2011) Chem Commun , vol.47 , pp. 6111-6113
    • Wang, G.W.1    Wang, C.Z.2    Zhu, S.E.3    Murata, Y.4
  • 35
    • 79961082590 scopus 로고    scopus 로고
    • Radical reaction of [60]fullerene with phosphorus compounds mediated by manganese(III) acetate
    • Wang GW, Wang CZ, Zou JP. Radical reaction of [60]fullerene with phosphorus compounds mediated by manganese(III) acetate. J Org Chem, 2011, 76: 6088-6094
    • (2011) J Org Chem , vol.76 , pp. 6088-6094
    • Wang, G.W.1    Wang, C.Z.2    Zou, J.P.3
  • 36
    • 80955155671 scopus 로고    scopus 로고
    • Synthesis of [60]fullerene-fused tetrahydronaphthalene and indane derivatives via a pathway switched by aluminum chloride
    • Liu TX, Li FB, Wang GW. Synthesis of [60]fullerene-fused tetrahydronaphthalene and indane derivatives via a pathway switched by aluminum chloride. Org Lett, 2011, 13: 6130-6133
    • (2011) Org Lett , vol.13 , pp. 6130-6133
    • Liu, T.X.1    Li, F.B.2    Wang, G.W.3
  • 37
    • 15444370105 scopus 로고    scopus 로고
    • One-pot sequential synthesis of acetoxylated [60]fullerene derivatives
    • Chen ZX, Wang GW. One-pot sequential synthesis of acetoxylated [60]fullerene derivatives. J Org Chem, 2005, 70: 2380-2383
    • (2005) J Org Chem , vol.70 , pp. 2380-2383
    • Chen, Z.X.1    Wang, G.W.2
  • 38
    • 33750042917 scopus 로고    scopus 로고
    • Approaches to open fullerenes: A 1, 2, 3, 4, 5, 6-hexaadduct of C60
    • Chuang SC, Clemente FR, Khan SI, Houk KN, Rubin Y. Approaches to open fullerenes: A 1, 2, 3, 4, 5, 6-hexaadduct of C60. Org Lett, 2006, 8: 4525-4528
    • (2006) Org Lett , vol.8 , pp. 4525-4528
    • Chuang, S.C.1    Clemente, F.R.2    Khan, S.I.3    Houk, K.N.4    Rubin, Y.5
  • 39
    • 50149086268 scopus 로고    scopus 로고
    • Decatungstate-mediated radical reactions of C60 with substituted toluenes and anisoles: A new photochemical functionalization strategy for fullerenes
    • Tzirakis MD, Orfanopoulos M. Decatungstate-mediated radical reactions of C60 with substituted toluenes and anisoles: A new photochemical functionalization strategy for fullerenes. Org Lett, 2008, 10: 873-876
    • (2008) Org Lett , vol.10 , pp. 873-876
    • Tzirakis, M.D.1    Orfanopoulos, M.2
  • 40
    • 67749120530 scopus 로고    scopus 로고
    • Acyl radical reactions in fullerene chemistry: Direct acylation of [60]fullerene through an efficient decatungstate-photomediated approach
    • Tzirakis MD, Orfanopoulos M. Acyl radical reactions in fullerene chemistry: Direct acylation of [60]fullerene through an efficient decatungstate-photomediated approach. J Am Chem Soc, 2009, 131: 4063-4069
    • (2009) J Am Chem Soc , vol.131 , pp. 4063-4069
    • Tzirakis, M.D.1    Orfanopoulos, M.2
  • 41
    • 77955568981 scopus 로고    scopus 로고
    • Photochemical addition of ethers to C60: Synthesis of the simplest [60]fullerene/crown ether conjugates
    • Tzirakis MD, Orfanopoulos M. Photochemical addition of ethers to C60: Synthesis of the simplest [60]fullerene/crown ether conjugates. Angew Chem Int Ed, 2010, 49: 5891-5893
    • (2010) Angew Chem Int Ed , vol.49 , pp. 5891-5893
    • Tzirakis, M.D.1    Orfanopoulos, M.2
  • 42
    • 77958489867 scopus 로고    scopus 로고
    • Hydroxyalkylation of [60]fullerene: Free radical addition of alcohols to C60
    • Tzirakis MD, Alberti MN, Orfanopoulos M. Hydroxyalkylation of [60]fullerene: Free radical addition of alcohols to C60. Chem Commun, 2010, 46: 8228-8230
    • (2010) Chem Commun , vol.46 , pp. 8228-8230
    • Tzirakis, M.D.1    Alberti, M.N.2    Orfanopoulos, M.3
  • 43
    • 0037073217 scopus 로고    scopus 로고
    • Fullerenes as a tert-butylperoxy radical trap, metal catalyzed reaction of tert-butyl hydroperoxide with fullerenes, and formation of the first fullerene mixed peroxides C60(O)(OOtBu)4 and C70(OOtBu)10
    • Gan L, Huang S, Zhang X, Zhang A, Cheng B, Cheng H, Li X, Shang G. Fullerenes as a tert-butylperoxy radical trap, metal catalyzed reaction of tert-butyl hydroperoxide with fullerenes, and formation of the first fullerene mixed peroxides C60(O)(OOtBu)4 and C70(OOtBu)10. J Am Chem Soc, 2002, 124: 13384-13385
    • (2002) J Am Chem Soc , vol.124 , pp. 13384-13385
    • Gan, L.1    Huang, S.2    Zhang, X.3    Zhang, A.4    Cheng, B.5    Cheng, H.6    Li, X.7    Shang, G.8
  • 44
    • 12144291591 scopus 로고    scopus 로고
    • Selective preparation of oxygen-rich [60]fullerene derivatives by stepwise addition of tert-butylperoxy radical and further functionalization of the fullerene mixed peroxides
    • Huang S, Xiao Z, Wang F, Gan L, Zhang X, Hu X, Zhang S, Lu M, Pan Q, Xu L. Selective preparation of oxygen-rich [60]fullerene derivatives by stepwise addition of tert-butylperoxy radical and further functionalization of the fullerene mixed peroxides. J Org Chem, 2004, 69: 2442-2453
    • (2004) J Org Chem , vol.69 , pp. 2442-2453
    • Huang, S.1    Xiao, Z.2    Wang, F.3    Gan, L.4    Zhang, X.5    Hu, X.6    Zhang, S.7    Lu, M.8    Pan, Q.9    Xu, L.10
  • 45
    • 0032563875 scopus 로고    scopus 로고
    • Activated carbon as the reagent for the oxidative cyclization of fullerene adducts
    • Bernstein R, Foote CS. Activated carbon as the reagent for the oxidative cyclization of fullerene adducts. Tetrahedron Lett, 1998, 39: 7051-7054
    • (1998) Tetrahedron Lett , vol.39 , pp. 7051-7054
    • Bernstein, R.1    Foote, C.S.2
  • 46
    • 62349120644 scopus 로고    scopus 로고
    • A facile access to [60]fullerene-fused δ-Lactones: Unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases
    • Wang GW, Zhu B. A facile access to [60]fullerene-fused δ-lactones: Unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases. Chem Commun, 2009, 1769-1771
    • (2009) Chem Commun , pp. 1769-1771
    • Wang, G.W.1    Zhu, B.2
  • 47
    • 78049487815 scopus 로고    scopus 로고
    • Synthesis of disubstituted [60]fullerenefused lactones: Ferric perchlorate-promoted reaction of [60]fullerene with malonate esters
    • Li FB, You X, Wang GW. Synthesis of disubstituted [60]fullerenefused lactones: Ferric perchlorate-promoted reaction of [60]fullerene with malonate esters. Org Lett, 2010, 12: 4896-4899
    • (2010) Org Lett , vol.12 , pp. 4896-4899
    • Li, F.B.1    You, X.2    Wang, G.W.3
  • 48
    • 34250885713 scopus 로고    scopus 로고
    • Novel functionalizations of [60]fullerenefused lactones
    • Wang GW, Li FB, Xu Y. Novel functionalizations of [60]fullerenefused lactones. J Org Chem, 2007, 72: 4774-4778
    • (2007) J Org Chem , vol.72 , pp. 4774-4778
    • Wang, G.W.1    Li, F.B.2    Xu, Y.3
  • 49
    • 0000171519 scopus 로고
    • Synthesis of substituted tetrahydronaphthalenes by Mn(III), Ce(IV), and Fe(III) oxidation of substituted diethyl α-benzylmalonates in the presence of olefins
    • Citterio A, Sebastiano R, Marion A, Santi R. Synthesis of substituted tetrahydronaphthalenes by Mn(III), Ce(IV), and Fe(III) oxidation of substituted diethyl α-benzylmalonates in the presence of olefins. J Org Chem, 1991, 56: 5328-5335
    • (1991) J Org Chem , vol.56 , pp. 5328-5335
    • Citterio, A.1    Sebastiano, R.2    Marion, A.3    Santi, R.4
  • 50
    • 0001177761 scopus 로고
    • Oxidation of diethyl (pyridylmethy1) malonates with Mn(III) acetate, Ce(IV) ammonium nitrate, and iron(III) perchlorate in the presence of alkenes and alkynes
    • Citterio A, Sebastiano R, Carvayal MC. Oxidation of diethyl (pyridylmethy1) malonates with Mn(III) acetate, Ce(IV) ammonium nitrate, and iron(III) perchlorate in the presence of alkenes and alkynes. J Org Chem, 1991, 56: 5335-5341
    • (1991) J Org Chem , vol.56 , pp. 5335-5341
    • Citterio, A.1    Sebastiano, R.2    Carvayal, M.C.3
  • 51
    • 84862189469 scopus 로고    scopus 로고
    • Ferric perchlorate-promoted reaction of [60]fullerene with β-keto esters
    • Li FB, Zhu SE, You X, Wang GW. Ferric perchlorate-promoted reaction of [60]fullerene with β-keto esters. Chin Sci Bull, 2012, 57: 2269-2272
    • (2012) Chin Sci Bull , vol.57 , pp. 2269-2272
    • Li, F.B.1    Zhu, S.E.2    You, X.3    Wang, G.W.4
  • 52
    • 0038032567 scopus 로고    scopus 로고
    • Base-catalysed oxidative [3+2] cycloaddition reaction of [60]fullerene with β-dicarbonyl compounds
    • Ohno M, Yashiro A, Eguchi S. Base-catalysed oxidative [3+2] cycloaddition reaction of [60]fullerene with β-dicarbonyl compounds. Chem Commun, 1996, 291-292
    • (1996) Chem Commun , pp. 291-292
    • Ohno, M.1    Yashiro, A.2    Eguchi, S.3
  • 53
    • 0038369779 scopus 로고    scopus 로고
    • Novel solvent-free reaction of C60 with active methylene compounds in the presence of Na2CO3 under high-speed vibration milling
    • Wang GW, Zhang TH, Li YJ, Lu P, Zhan H, Liu YC, Murata Y, Komatasu K. Novel solvent-free reaction of C60 with active methylene compounds in the presence of Na2CO3 under high-speed vibration milling. Tetrahedron Lett, 2003, 44: 4407-4409
    • (2003) Tetrahedron Lett , vol.44 , pp. 4407-4409
    • Wang, G.W.1    Zhang, T.H.2    Li, Y.J.3    Lu, P.4    Zhan, H.5    Liu, Y.C.6    Murata, Y.7    Komatasu, K.8
  • 54
    • 3042760288 scopus 로고    scopus 로고
    • Solvent-free reactions of C60 with active methylene compounds, either with or without carbon tetrabromide, in the presence of bases under high-speed vibration milling conditions
    • Zhang TH, Wang GW, Lu P, Li YJ, Peng RF, Liu YC, Murata Y, Komatsu K. Solvent-free reactions of C60 with active methylene compounds, either with or without carbon tetrabromide, in the presence of bases under high-speed vibration milling conditions. Org Biomol Chem, 2004, 2: 1698-1702
    • (2004) Org Biomol Chem , vol.2 , pp. 1698-1702
    • Zhang, T.H.1    Wang, G.W.2    Lu, P.3    Li, Y.J.4    Peng, R.F.5    Liu, Y.C.6    Murata, Y.7    Komatsu, K.8
  • 55
    • 50149104769 scopus 로고    scopus 로고
    • Synthesis of fullerooxazoles: Novel reactions of [60]fullerene with nitriles promoted by ferric perchlorate
    • Li FB, Liu TX, Wang GW. Synthesis of fullerooxazoles: Novel reactions of [60]fullerene with nitriles promoted by ferric perchlorate. J Org Chem, 2008, 73: 6417-6420
    • (2008) J Org Chem , vol.73 , pp. 6417-6420
    • Li, F.B.1    Liu, T.X.2    Wang, G.W.3
  • 56
    • 0028900556 scopus 로고
    • Addition of photochemically generated acylnitrenes to C60: Synthesis of fulleroaziridines and thermal rearrangement to fullerooxazoles
    • Averdung J, Mattay J, Jacobi D, Abraham W. Addition of photochemically generated acylnitrenes to C60: Synthesis of fulleroaziridines and thermal rearrangement to fullerooxazoles. Tetrahedron, 1995, 51: 2543-2552
    • (1995) Tetrahedron , vol.51 , pp. 2543-2552
    • Averdung, J.1    Mattay, J.2    Jacobi, D.3    Abraham, W.4
  • 59
    • 0036589307 scopus 로고    scopus 로고
    • Additions to metal-activated organonitriles
    • Kukushkin Vyu, Pombeiro AJL. Additions to metal-activated organonitriles. Chem Rev, 2002, 102: 1771-1802
    • (2002) Chem Rev , vol.102 , pp. 1771-1802
    • Kukushkin, V.Y.1    Pombeiro, A.J.L.2
  • 60
    • 77954548436 scopus 로고    scopus 로고
    • A facile access to [60]fullerenefused 1, 3-dioxolanes: Reaction of [60]fullerene with aldehydes/ ketones promoted by ferric perchlorate
    • Li FB, Liu TX, You X, Wang GW. A facile access to [60]fullerenefused 1, 3-dioxolanes: Reaction of [60]fullerene with aldehydes/ ketones promoted by ferric perchlorate. Org Lett, 2010, 12: 3258-3261
    • (2010) Org Lett , vol.12 , pp. 3258-3261
    • Li, F.B.1    Liu, T.X.2    You, X.3    Wang, G.W.4
  • 62
    • 0027482653 scopus 로고
    • Reaction of C60 with diacyl peroxides containing perfluoroalkyl groups: The first example of electron transfer reaction via C60 +· in solution
    • Yoshida M, Morinaga Y, Iyoda M, Kikuchi K, Ikemodo I, Achiba Y. Reaction of C60 with diacyl peroxides containing perfluoroalkyl groups: The first example of electron transfer reaction via C60 +· in solution. Tetrahedron Lett, 1993, 34: 7629-7632
    • (1993) Tetrahedron Lett , vol.34 , pp. 7629-7632
    • Yoshida, M.1    Morinaga, Y.2    Iyoda, M.3    Kikuchi, K.4    Ikemodo, I.5    Achiba, Y.6
  • 63
    • 37049072833 scopus 로고
    • Reaction of sodium alkoxides with [60]fullerene: Formation of a 1, 3-dioxolane derivative and involvement of O2 in a nucleophilic addition reaction of C60
    • Wang GW, Shu LH, Wu SH, Wu HM, Lao XF. Reaction of sodium alkoxides with [60]fullerene: Formation of a 1, 3-dioxolane derivative and involvement of O2 in a nucleophilic addition reaction of C60. J Chem Soc Chem Commun, 1995, 1071-1072
    • (1995) J Chem Soc Chem Commun , pp. 1071-1072
    • Wang, G.W.1    Shu, L.H.2    Wu, S.H.3    Wu, H.M.4    Lao, X.F.5
  • 64
    • 14844323718 scopus 로고    scopus 로고
    • Efficient acetalization of epoxy rings on a fullerene cage
    • Shigemitsu Y, Kaneko M, Tajima Y, Takeuchi K. Efficient acetalization of epoxy rings on a fullerene cage. Chem Lett, 2004, 33: 1604-1605
    • (2004) Chem Lett , vol.33 , pp. 1604-1605
    • Shigemitsu, Y.1    Kaneko, M.2    Tajima, Y.3    Takeuchi, K.4
  • 65
    • 33645229308 scopus 로고    scopus 로고
    • Reaction of [60]fullerene with CF3COOHal affords an unusual 1, 3-dioxolano-[60]fullerene
    • Troshin PA, Peregudov AS, Lyubovskaya RN. Reaction of [60]fullerene with CF3COOHal affords an unusual 1, 3-dioxolano-[60]fullerene. Tetrahedron Lett, 2006, 47: 2969-2972
    • (2006) Tetrahedron Lett , vol.47 , pp. 2969-2972
    • Troshin, P.A.1    Peregudov, A.S.2    Lyubovskaya, R.N.3
  • 66
    • 41649107337 scopus 로고    scopus 로고
    • Reactivity of fullerene epoxide: Preparation of fullerene-fused thiirane, tetrahydrothiazolidin-2-one, and 1, 3-dioxolane
    • Yang X, Huang S, Jia Z, Xiao Z, Jiang Z, Zhang Q, Gan L, Zheng B, Yuan G, Zhang S. Reactivity of fullerene epoxide: Preparation of fullerene-fused thiirane, tetrahydrothiazolidin-2-one, and 1, 3-dioxolane. J Org Chem, 2008, 73: 2518-2526
    • (2008) J Org Chem , vol.73 , pp. 2518-2526
    • Yang, X.1    Huang, S.2    Jia, Z.3    Xiao, Z.4    Jiang, Z.5    Zhang, Q.6    Gan, L.7    Zheng, B.8    Yuan, G.9    Zhang, S.10
  • 67
    • 84859600878 scopus 로고    scopus 로고
    • Fullerenyl boronic esters: Ferric perchlorate-mediated synthesis and functionalization
    • Li FB, You X, Liu TX, Wang GW. Fullerenyl boronic esters: Ferric perchlorate-mediated synthesis and functionalization. Org Lett, 2012, 14: 1800-1803
    • (2012) Org Lett , vol.14 , pp. 1800-1803
    • Li, F.B.1    You, X.2    Liu, T.X.3    Wang, G.W.4
  • 68
    • 7044263179 scopus 로고    scopus 로고
    • The relationship among pKa, pH, and binding constants in the interactions between boronic acids and diols-It is not as simple as it appears
    • Yan J, Springsteen G, Deeter S, Wang B. The relationship among pKa, pH, and binding constants in the interactions between boronic acids and diols-It is not as simple as it appears. Tetrahedron, 2004, 60: 11205-11209
    • (2004) Tetrahedron , vol.60 , pp. 11205-11209
    • Yan, J.1    Springsteen, G.2    Deeter, S.3    Wang, B.4
  • 69
    • 61349159292 scopus 로고    scopus 로고
    • A bench-stable Pd catalyst for the hydroarylation of fullerene with boronic acids
    • Mori S, Nambo M, Chi LC, Bouffard J, Itami K. A bench-stable Pd catalyst for the hydroarylation of fullerene with boronic acids. Org Lett, 2008, 10: 4609-4612
    • (2008) Org Lett , vol.10 , pp. 4609-4612
    • Mori, S.1    Nambo, M.2    Chi, L.C.3    Bouffard, J.4    Itami, K.5
  • 70
    • 34447115833 scopus 로고    scopus 로고
    • Rh-catalyzed arylation and alkenylation of C60 using organoboron compounds
    • Nambo M, Noyori R, Itami K. Rh-catalyzed arylation and alkenylation of C60 using organoboron compounds. J Am Chem Soc, 2007, 129: 8080-8081
    • (2007) J Am Chem Soc , vol.129 , pp. 8080-8081
    • Nambo, M.1    Noyori, R.2    Itami, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.