메뉴 건너뛰기




Volumn 40, Issue 14, 2010, Pages 2122-2129

Triton B-mediated efficient and convenient alkoxylation of activated aryl and heteroaryl halides

Author keywords

Alkoxylation; Aryl halides; Ethers; Triton B

Indexed keywords

ALCOHOL; ETHER DERIVATIVE; HALIDE; TRITON B; TYLOXAPOL; UNCLASSIFIED DRUG;

EID: 77953711531     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903219518     Document Type: Article
Times cited : (13)

References (22)
  • 1
    • 17444373975 scopus 로고    scopus 로고
    • Synthesis of alkyl ethers by catalytic Williamson ether synthesis with weak alkylation agents
    • Fuhrmann, E.; Talbiersky, J. Synthesis of alkyl ethers by catalytic Williamson ether synthesis with weak alkylation agents. Org. Process Res. Develop. 2005, 9, 206-211.
    • (2005) Org. Process Res. Develop. , vol.9 , pp. 206-211
    • Fuhrmann, E.1    Talbiersky, J.2
  • 3
  • 5
    • 41649095662 scopus 로고    scopus 로고
    • An efficient intermolecular BINAM-copper (I)-catalyzed Ullmann-type coupling of aryl iodides=bromides with aliphatic alcohols
    • Naidu, A. B.; Sekar, G. An efficient intermolecular BINAM-copper (I)-catalyzed Ullmann-type coupling of aryl iodides=bromides with aliphatic alcohols. Tetrahedron Lett. 2008, 49, 3147.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 3147
    • Naidu, A.B.1    Sekar, G.2
  • 6
    • 0001541326 scopus 로고    scopus 로고
    • Dimethyl carbonate for environmentally benign reactions
    • Ono, Y. Dimethyl carbonate for environmentally benign reactions. Pure Appl. Chem. 1996, 68, 367-375.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 367-375
    • Ono, Y.1
  • 7
    • 12344337315 scopus 로고    scopus 로고
    • Palladium-catalyzed C-N and C-O coupling: A practical guide from an industrial vantage point
    • Schlummer, B.; Scholz, U. Palladium-catalyzed C-N and C-O coupling: A practical guide from an industrial vantage point. Adv. Synth. Catal. 2004, 346, 1599-1626.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1599-1626
    • Schlummer, B.1    Scholz, U.2
  • 8
    • 0035815141 scopus 로고    scopus 로고
    • Palladium-catalyzed formation of aryl tert-butyl ethers from unactivated aryl halides
    • Parrish, C. A.; Buchwald, S. L. Palladium-catalyzed formation of aryl tert-butyl ethers from unactivated aryl halides. J. Org. Chem. 2001, 66, 2498-2500.
    • (2001) J. Org. Chem. , vol.66 , pp. 2498-2500
    • Parrish, C.A.1    Buchwald, S.L.2
  • 9
    • 33845479686 scopus 로고    scopus 로고
    • Palladium-catalyzed C-O bond formation: Direct synthesis of phenols and aryl=alkyl ethers from activated aryl halides
    • Chen, G.; Chan, A. S. C.; Kwong, F. Y. L. Palladium-catalyzed C-O bond formation: Direct synthesis of phenols and aryl=alkyl ethers from activated aryl halides. Tetrahedron Lett. 2007, 48, 473-476.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 473-476
    • Chen, G.1    Chan, A.S.C.2    Kwong, F.Y.L.3
  • 10
    • 7444267299 scopus 로고    scopus 로고
    • Zinc-catalyzed Williamson ether synthesis in the absence of base
    • Paul, S.; Gupt, M. Zinc-catalyzed Williamson ether synthesis in the absence of base. Tetrahedron Lett. 2004, 48, 8825-8829.
    • (2004) Tetrahedron Lett. , vol.48 , pp. 8825-8829
    • Paul, S.1    Gupt, M.2
  • 11
    • 0000416587 scopus 로고    scopus 로고
    • O-alkylation of phenol derivatives over basic zeolites
    • Lee, S.; Lee, S. W.; Kim, K. S.; Lee, J. J.; Hyun, D.; Kim, J. C. O-alkylation of phenol derivatives over basic zeolites. Catal. Today 1998, 44, 253-258.
    • (1998) Catal. Today , vol.44 , pp. 253-258
    • Lee, S.1    Lee, S.W.2    Kim, K.S.3    Lee, J.J.4    Hyun, D.5    Kim, J.C.6
  • 12
    • 0037471219 scopus 로고    scopus 로고
    • Transition-metal-free Suzuki-type coupling reactions
    • Leadbeater, N. E.; Marco, M. Transition-metal-free Suzuki-type coupling reactions. Angew. Chem. Int. Ed. 2003, 42, 1407.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1407
    • Leadbeater, N.E.1    Marco, M.2
  • 14
    • 0036115764 scopus 로고    scopus 로고
    • Synthesis and reactivity of 1,4-oxazinoindole derivatives
    • Mayer, S.; Merour, J.-Y.; Joseph, B.; Guillamet, G. Synthesis and reactivity of 1,4-oxazinoindole derivatives. Eur. J. Org. Chem. 2002, 10, 1646-1653.
    • (2002) Eur. J. Org. Chem. , vol.10 , pp. 1646-1653
    • Mayer, S.1    Merour, J.-Y.2    Joseph, B.3    Guillamet, G.4
  • 16
    • 33645548790 scopus 로고    scopus 로고
    • A high yielding, one-pot, Triton-B-catalyzed synthesis of dithiocarbamates using alcoholic tosylates
    • Chaturvedi, D.; Ray, S. A high yielding, one-pot, Triton-B-catalyzed synthesis of dithiocarbamates using alcoholic tosylates. Monatsh. Chem. 2006, 137, 465-469.
    • (2006) Monatsh. Chem. , vol.137 , pp. 465-469
    • Chaturvedi, D.1    Ray, S.2
  • 17
    • 0030804668 scopus 로고    scopus 로고
    • Solid state deoximation with ammonium persulfate-silica gel: Regeneration of carbonyl compounds using microwaves
    • Varma, R. S.; Meshram, H. M. Solid state deoximation with ammonium persulfate-silica gel: Regeneration of carbonyl compounds using microwaves. Tetrahedron Lett. 1997, 38, 5427-5428;
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5427-5428
    • Varma, R.S.1    Meshram, H.M.2
  • 18
    • 0030856871 scopus 로고    scopus 로고
    • Solid state cleavage of semicarbazones and phenylhydrazones with ammonium persulfate-clay using microwave or ultrasonic irradiation
    • Varma, R. S.; Meshram, H. M. Solid state cleavage of semicarbazones and phenylhydrazones with ammonium persulfate-clay using microwave or ultrasonic irradiation. Tetrahedron Lett. 1997, 38, 7973-7976;
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7973-7976
    • Varma, R.S.1    Meshram, H.M.2
  • 19
    • 0030830365 scopus 로고    scopus 로고
    • Clay-supported ammonium nitrate "clayan": A mild and eco-friendly reagent for dethioacetalization
    • Meshram, H. M.; Reddy, G. S.; Yadav, J. S. Clay-supported ammonium nitrate "Clayan": A mild and eco-friendly reagent for dethioacetalization. Tetrahedron Lett. 1997, 38, 8891-8894;
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8891-8894
    • Meshram, H.M.1    Reddy, G.S.2    Yadav, J.S.3
  • 20
    • 0041562608 scopus 로고    scopus 로고
    • Clay-supported ammonium nitrate "clayan": A new reagent for selective nitration of arenes
    • Meshram, H. M.; Ganesh, Y. S. S.; Yadav, J. S. Clay-supported ammonium nitrate "Clayan": A new reagent for selective nitration of arenes. Synth. Commun. 2003, 33, 2497-2503.
    • (2003) Synth. Commun. , vol.33 , pp. 2497-2503
    • Meshram, H.M.1    Ganesh, Y.S.S.2    Yadav, J.S.3
  • 21
    • 33845479686 scopus 로고    scopus 로고
    • Palladium-catalyzed C-O bond formation: Direct synthesis of phenols and aryl=alkyl ethers from activated aryl halides
    • Chen, G.; Chan, A. S. C.; Kwong, F. Y. Palladium-catalyzed C-O bond formation: Direct synthesis of phenols and aryl=alkyl ethers from activated aryl halides. Tetrahedron Lett. 2007, 48, 473-476;
    • (2007) Tetrahedron Lett. , vol.48 , pp. 473-476
    • Chen, G.1    Chan, A.S.C.2    Kwong, F.Y.3
  • 22
    • 0037149634 scopus 로고    scopus 로고
    • Copper-catalyzed coupling of aryl iodides with aliphatic alcohols
    • Wolter, G.; Nordmann, M.; Job, G. E.; Buchwald, S. L. Copper-catalyzed coupling of aryl iodides with aliphatic alcohols. Org. Lett. 2002, 4, 973-976.
    • (2002) Org. Lett. , vol.4 , pp. 973-976
    • Wolter, G.1    Nordmann, M.2    Job, G.E.3    Buchwald, S.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.