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Volumn 3, Issue 11, 2015, Pages 3004-3011

Catalytic Rearrangement of Aldoximes to Primary Amides in Environmentally Friendly Media under Thermal and Microwave Heating: Another Application of the Bis(allyl)-Ruthenium(IV) Dimer [{RuCl(μ-Cl)(η3:η3-C10H16)}2]

Author keywords

Green solvents; Microwave heating; Rearrangement of aldoximes; Ruthenium catalysts; Synthesis of amides

Indexed keywords

AMIDES; CATALYSTS; CHLORINE COMPOUNDS; RUTHENIUM; RUTHENIUM COMPOUNDS;

EID: 84946201886     PISSN: None     EISSN: 21680485     Source Type: Journal    
DOI: 10.1021/acssuschemeng.5b01107     Document Type: Article
Times cited : (26)

References (54)
  • 1
    • 84881409062 scopus 로고    scopus 로고
    • The National Science Foundation's Investment in Sustainable Chemistry, Engineering, and Materials
    • White, A. A.; Platz, M. S.; Aruguete, D. M.; Jones, S. L.; Madsen, L. D.; Wesson, R. D. The National Science Foundation's Investment in Sustainable Chemistry, Engineering, and Materials ACS Sustainable Chem. Eng. 2013, 1 (8) 871-877 10.1021/sc400002r
    • (2013) ACS Sustainable Chem. Eng. , vol.1 , Issue.8 , pp. 871-877
    • White, A.A.1    Platz, M.S.2    Aruguete, D.M.3    Jones, S.L.4    Madsen, L.D.5    Wesson, R.D.6
  • 2
    • 84931421134 scopus 로고    scopus 로고
    • Cambridge University Press: Cambridge, U.K.
    • de Vries, B. J. M. Sustainability Science; Cambridge University Press: Cambridge, U.K., 2013.
    • (2013) Sustainability Science
    • De Vries, B.J.M.1
  • 4
    • 0037008514 scopus 로고    scopus 로고
    • Green Chemistry: Science and Politics of Change
    • Poliakoff, M.; Fitzpatrick, J. M.; Farren, T. R.; Anastas, P. T. Green Chemistry: Science and Politics of Change Science 2002, 297 (5582) 807-810 10.1126/science.297.5582.807
    • (2002) Science , vol.297 , Issue.5582 , pp. 807-810
    • Poliakoff, M.1    Fitzpatrick, J.M.2    Farren, T.R.3    Anastas, P.T.4
  • 11
    • 77954592787 scopus 로고    scopus 로고
    • Glycerol as a Sustainable Solvent for Green Chemistry
    • Gu, Y.; Jéroîme, F. Glycerol as a Sustainable Solvent for Green Chemistry Green Chem. 2010, 12 (7) 1127-1138 10.1039/c001628d
    • (2010) Green Chem. , vol.12 , Issue.7 , pp. 1127-1138
    • Gu, Y.1    Jéroîme, F.2
  • 12
    • 79957496356 scopus 로고    scopus 로고
    • Glycerol and Derived Solvents: New Sustainable Reaction Media for Organic Synthesis
    • Díaz-álvarez, A. E.; Francos, J.; Lastra-Barreira, B.; Crochet, P.; Cadierno, V. Glycerol and Derived Solvents: New Sustainable Reaction Media for Organic Synthesis Chem. Commun. 2011, 47 (22) 6208-6227 10.1039/c1cc10620a
    • (2011) Chem. Commun. , vol.47 , Issue.22 , pp. 6208-6227
    • Díaz-Álvarez, A.E.1    Francos, J.2    Lastra-Barreira, B.3    Crochet, P.4    Cadierno, V.5
  • 13
    • 84887931515 scopus 로고    scopus 로고
    • Glycerol-Based Solvents in Organic Synthesis
    • Wolfson, A.; Dlugy, C.; Tavor, D. Glycerol-Based Solvents in Organic Synthesis Trends Org. Chem. 2011, 15, 41-50
    • (2011) Trends Org. Chem. , vol.15 , pp. 41-50
    • Wolfson, A.1    Dlugy, C.2    Tavor, D.3
  • 14
    • 84885880358 scopus 로고    scopus 로고
    • Glycerol: A Promising Green Solvent and Reducing Agent for Metal-Catalyzed Transfer Hydrogenation Reactions and Nanoparticles Formation
    • Díaz-álvarez, A. E.; Cadierno, V. Glycerol: A Promising Green Solvent and Reducing Agent for Metal-Catalyzed Transfer Hydrogenation Reactions and Nanoparticles Formation Appl. Sci. 2013, 3 (1) 55-69 10.3390/app3010055
    • (2013) Appl. Sci. , vol.3 , Issue.1 , pp. 55-69
    • Díaz-Álvarez, A.E.1    Cadierno, V.2
  • 15
    • 84894609445 scopus 로고    scopus 로고
    • Glycerol Based Solvents: Synthesis, Properties and Applications
    • García, J. I.; García-Marín, H.; Pires, E. Glycerol Based Solvents: Synthesis, Properties and Applications Green Chem. 2014, 16 (3) 1007-1033 10.1039/c3gc41857j
    • (2014) Green Chem. , vol.16 , Issue.3 , pp. 1007-1033
    • García, J.I.1    García-Marín, H.2    Pires, E.3
  • 16
    • 84906787427 scopus 로고    scopus 로고
    • Glycerol as Sustainable Solvent for the Synthesis of Metallic Species and Catalysis
    • Chahdoura, F.; Favier, I.; Gómez, M. Glycerol as Sustainable Solvent for the Synthesis of Metallic Species and Catalysis Chem.-Eur. J. 2014, 20 (35) 10884-10893 10.1002/chem.201403534
    • (2014) Chem. - Eur. J. , vol.20 , Issue.35 , pp. 10884-10893
    • Chahdoura, F.1    Favier, I.2    Gómez, M.3
  • 17
    • 84903192389 scopus 로고    scopus 로고
    • Recent Advances in the Use of Glycerol as Green Solvent for Synthetic Organic Chemistry
    • Díaz-álvarez, A. E.; Francos, J.; Crochet, P.; Cadierno, V. Recent Advances in the Use of Glycerol as Green Solvent for Synthetic Organic Chemistry Curr. Green Chem. 2014, 1 (1) 51-65 10.2174/221334610101131218094907
    • (2014) Curr. Green Chem. , vol.1 , Issue.1 , pp. 51-65
    • Díaz-Álvarez, A.E.1    Francos, J.2    Crochet, P.3    Cadierno, V.4
  • 18
    • 34447097175 scopus 로고    scopus 로고
    • Microwave-Assisted Synthesis in Water as Solvent
    • Dallinger, D.; Kappe, C. O. Microwave-Assisted Synthesis in Water as Solvent Chem. Rev. 2007, 107 (6) 2563-2591 10.1021/cr0509410
    • (2007) Chem. Rev. , vol.107 , Issue.6 , pp. 2563-2591
    • Dallinger, D.1    Kappe, C.O.2
  • 20
    • 84894639917 scopus 로고    scopus 로고
    • Glycerol: A Solvent and Building Block of Choice for Microwave and Ultrasound Irradiation Procedures
    • Cintas, P.; Tagliapietra, S.; Gaudino, E. C.; Palmisano, G.; Cravotto, G. Glycerol: A Solvent and Building Block of Choice for Microwave and Ultrasound Irradiation Procedures Green Chem. 2014, 16 (3) 1056-1065 10.1039/c3gc41955j
    • (2014) Green Chem. , vol.16 , Issue.3 , pp. 1056-1065
    • Cintas, P.1    Tagliapietra, S.2    Gaudino, E.C.3    Palmisano, G.4    Cravotto, G.5
  • 21
    • 84923025771 scopus 로고    scopus 로고
    • Microwave-Assisted Synthesis - Catalytic Applications in Aqueous Media
    • Rathi, A. K.; Gawande, M. B.; Zboril, R.; Varma, R. S. Microwave-Assisted Synthesis-Catalytic Applications in Aqueous Media Coord. Chem. Rev. 2015, 291, 68-94 10.1016/j.ccr.2015.01.011
    • (2015) Coord. Chem. Rev. , vol.291 , pp. 68-94
    • Rathi, A.K.1    Gawande, M.B.2    Zboril, R.3    Varma, R.S.4
  • 24
    • 84872375024 scopus 로고    scopus 로고
    • Microwave Effects in Organic Synthesis: Myth or Reality?
    • Kappe, C. O.; Pieber, B.; Dallinger, D. Microwave Effects in Organic Synthesis: Myth or Reality? Angew. Chem., Int. Ed. 2013, 52 (4) 1088-1094 10.1002/anie.201204103
    • (2013) Angew. Chem., Int. Ed. , vol.52 , Issue.4 , pp. 1088-1094
    • Kappe, C.O.1    Pieber, B.2    Dallinger, D.3
  • 25
    • 23044467627 scopus 로고    scopus 로고
    • Energy Efficiency in Chemical Reactions: A Comparative Study of Different Reaction Techniques
    • Gronnow, M. J.; White, R. J.; Clark, J. H.; Macquarrie, D. J. Energy Efficiency in Chemical Reactions: A Comparative Study of Different Reaction Techniques Org. Process Res. Dev. 2005, 9 (4) 516-518 10.1021/op0498060
    • (2005) Org. Process Res. Dev. , vol.9 , Issue.4 , pp. 516-518
    • Gronnow, M.J.1    White, R.J.2    Clark, J.H.3    Macquarrie, D.J.4
  • 27
    • 31944440710 scopus 로고    scopus 로고
    • Bis(allyl)-Ruthenium(IV) Complexes as Highly Efficient Catalysts for the Redox Isomerization of Allylic Alcohols into Carbonyl Compounds in Organic and Aqueous Media: Scope, Limitations and Theoretical Analysis of the Mechanism
    • Cadierno, V.; García-Garrido, S. E.; Gimeno, J.; Varela-álvarez, A.; Sordo, J. A. Bis(allyl)-Ruthenium(IV) Complexes as Highly Efficient Catalysts for the Redox Isomerization of Allylic Alcohols into Carbonyl Compounds in Organic and Aqueous Media: Scope, Limitations and Theoretical Analysis of the Mechanism J. Am. Chem. Soc. 2006, 128 (4) 1360-1370 10.1021/ja054827a
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.4 , pp. 1360-1370
    • Cadierno, V.1    García-Garrido, S.E.2    Gimeno, J.3    Varela-Álvarez, A.4    Sordo, J.A.5
  • 28
    • 80052508449 scopus 로고    scopus 로고
    • Ruthenium(IV)-Catalyzed Isomerization of the C=C Bond of O-Allylic Substrates: A Theoretical and Experimental Study
    • Varela-álvarez, A.; Sordo, J. A.; Piedra, E.; Nebra, N.; Cadierno, V.; Gimeno, J. Ruthenium(IV)-Catalyzed Isomerization of the C=C Bond of O-Allylic Substrates: A Theoretical and Experimental Study Chem.-Eur. J. 2011, 17 (38) 10583-10599 10.1002/chem.201101131
    • (2011) Chem. - Eur. J. , vol.17 , Issue.38 , pp. 10583-10599
    • Varela-Álvarez, A.1    Sordo, J.A.2    Piedra, E.3    Nebra, N.4    Cadierno, V.5    Gimeno, J.6
  • 29
    • 79751482501 scopus 로고    scopus 로고
    • Ruthenium(IV) Catalysts for the Selective Estragole to Trans-Anethole Isomerization in Environmentally Friendly Media
    • Lastra-Barreira, B.; Francos, J.; Crochet, P.; Cadierno, V. Ruthenium(IV) Catalysts for the Selective Estragole to Trans-Anethole Isomerization in Environmentally Friendly Media Green Chem. 2011, 13 (2) 307-313 10.1039/C0GC00417K
    • (2011) Green Chem. , vol.13 , Issue.2 , pp. 307-313
    • Lastra-Barreira, B.1    Francos, J.2    Crochet, P.3    Cadierno, V.4
  • 30
    • 84857633385 scopus 로고    scopus 로고
    • A General Route for the Stereoselective Synthesis of (E)-(1-Propenyl)phenyl Esters by Catalytic C=C Bond Isomerization
    • Díaz-álvarez, A. E.; Crochet, P.; Cadierno, V. A General Route for the Stereoselective Synthesis of (E)-(1-Propenyl)phenyl Esters by Catalytic C=C Bond Isomerization Tetrahedron 2012, 68 (12) 2611-2620 10.1016/j.tet.2012.01.083
    • (2012) Tetrahedron , vol.68 , Issue.12 , pp. 2611-2620
    • Díaz-Álvarez, A.E.1    Crochet, P.2    Cadierno, V.3
  • 31
    • 23944483168 scopus 로고    scopus 로고
    • Ru(IV)-Catalyzed Isomerization of Allylamines in Water: A Highly Efficient Procedure for the Deprotection of N-Allylic Amides
    • Cadierno, V.; García-Garrido, S. E.; Gimeno, J.; Nebra, N. Ru(IV)-Catalyzed Isomerization of Allylamines in Water: A Highly Efficient Procedure for the Deprotection of N-Allylic Amides Chem. Commun. 2005, 32, 4086-4088 10.1039/b506788j
    • (2005) Chem. Commun. , vol.32 , pp. 4086-4088
    • Cadierno, V.1    García-Garrido, S.E.2    Gimeno, J.3    Nebra, N.4
  • 33
    • 79951927813 scopus 로고    scopus 로고
    • Ruthenium(IV)-Catalyzed Markovnikov Addition of Carboxylic Acids to Terminal Alkynes in Aqueous Medium
    • Cadierno, V.; Francos, J.; Gimeno, J. Ruthenium(IV)-Catalyzed Markovnikov Addition of Carboxylic Acids to Terminal Alkynes in Aqueous Medium Organometallics 2011, 30 (4) 852-862 10.1021/om1010325
    • (2011) Organometallics , vol.30 , Issue.4 , pp. 852-862
    • Cadierno, V.1    Francos, J.2    Gimeno, J.3
  • 34
    • 84915804490 scopus 로고    scopus 로고
    • Asymmetric Hydrogenation of 1-Alkyl and 1-Aryl Vinyl Benzoates: A Broad Scope Procedure for the Highly Enantioselective Synthesis of 1-Substituted Ethyl Benzoates
    • Kleman, P.; González-Liste, P. J.; García-Garrido, S. E.; Cadierno, V.; Pizzano, A. Asymmetric Hydrogenation of 1-Alkyl and 1-Aryl Vinyl Benzoates: A Broad Scope Procedure for the Highly Enantioselective Synthesis of 1-Substituted Ethyl Benzoates ACS Catal. 2014, 4 (12) 4398-4408 10.1021/cs501402z
    • (2014) ACS Catal. , vol.4 , Issue.12 , pp. 4398-4408
    • Kleman, P.1    González-Liste, P.J.2    García-Garrido, S.E.3    Cadierno, V.4    Pizzano, A.5
  • 35
    • 77955872800 scopus 로고    scopus 로고
    • Bis(allyl)ruthenium(IV) Complexes Containing Water-Soluble Phosphane Ligands: Synthesis, Structure, and Application as Catalysts in the Selective Hydration of Organonitriles into Amides
    • Cadierno, V.; Díez, J.; Francos, J.; Gimeno, J. Bis(allyl)ruthenium(IV) Complexes Containing Water-Soluble Phosphane Ligands: Synthesis, Structure, and Application as Catalysts in the Selective Hydration of Organonitriles into Amides Chem.-Eur. J. 2010, 16 (32) 9808-9817 10.1002/chem.201001152
    • (2010) Chem. - Eur. J. , vol.16 , Issue.32 , pp. 9808-9817
    • Cadierno, V.1    Díez, J.2    Francos, J.3    Gimeno, J.4
  • 36
    • 84905059008 scopus 로고    scopus 로고
    • An Efficient Ruthenium(IV) Catalyst for the Selective Hydration of Nitriles to Amides in Water under Mild Conditions
    • Tomás-Mendivil, E.; Suárez, F. J.; Díez, J.; Cadierno, V. An Efficient Ruthenium(IV) Catalyst for the Selective Hydration of Nitriles to Amides in Water under Mild Conditions Chem. Commun. 2014, 50 (68) 9661-9664 10.1039/C4CC04058A
    • (2014) Chem. Commun. , vol.50 , Issue.68 , pp. 9661-9664
    • Tomás-Mendivil, E.1    Suárez, F.J.2    Díez, J.3    Cadierno, V.4
  • 37
    • 77953215073 scopus 로고    scopus 로고
    • Ruthenium/TFA-Catalyzed Regioselective C-3-Alkylation of Indoles with Terminal Alkynes in Water: Efficient and Unprecedented Access to 3-(1-Methylalkyl)-1H-indoles
    • Cadierno, V.; Francos, J.; Gimeno, J. Ruthenium/TFA-Catalyzed Regioselective C-3-Alkylation of Indoles with Terminal Alkynes in Water: Efficient and Unprecedented Access to 3-(1-Methylalkyl)-1H-indoles Chem. Commun. 2010, 46 (23) 4175-4177 10.1039/c002804e
    • (2010) Chem. Commun. , vol.46 , Issue.23 , pp. 4175-4177
    • Cadierno, V.1    Francos, J.2    Gimeno, J.3
  • 38
    • 33845205545 scopus 로고    scopus 로고
    • Efficient Intermolecular [2 + 2 + 2] Alkyne Cyclotrimerization in Aqueous Medium Using a Ruthenium(IV) Precatalyst
    • Cadierno, V.; García-Garrido, S. E.; Gimeno, J. Efficient Intermolecular [2 + 2 + 2] Alkyne Cyclotrimerization in Aqueous Medium Using a Ruthenium(IV) Precatalyst J. Am. Chem. Soc. 2006, 128 (47) 15094-15095 10.1021/ja066552k
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.47 , pp. 15094-15095
    • Cadierno, V.1    García-Garrido, S.E.2    Gimeno, J.3
  • 39
    • 79951999305 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Intermolecular [2 + 2 + 2] Alkyne Cyclotrimerization in Aqueous Media under Microwave Irradiation
    • Cadierno, V.; Francos, J.; García-Garrido, S. E.; Gimeno, J. Ruthenium-Catalyzed Intermolecular [2 + 2 + 2] Alkyne Cyclotrimerization in Aqueous Media under Microwave Irradiation Green Chem. Lett. Rev. 2011, 4 (1) 55-61 10.1080/17518253.2010.500623
    • (2011) Green Chem. Lett. Rev. , vol.4 , Issue.1 , pp. 55-61
    • Cadierno, V.1    Francos, J.2    García-Garrido, S.E.3    Gimeno, J.4
  • 40
    • 79959403001 scopus 로고    scopus 로고
    • Metal-Catalysed Approaches to Amide Bond Formation
    • Allen, C. L.; Williams, J. M. J. Metal-Catalysed Approaches to Amide Bond Formation Chem. Soc. Rev. 2011, 40 (7) 3405-3415 10.1039/c0cs00196a
    • (2011) Chem. Soc. Rev. , vol.40 , Issue.7 , pp. 3405-3415
    • Allen, C.L.1    Williams, J.M.J.2
  • 41
    • 84871794514 scopus 로고    scopus 로고
    • Metal-Catalyzed Amide Bond Forming Reactions in an Environmentally Friendly Aqueous Medium: Nitrile Hydrations and Beyond
    • García-álvarez, R.; Crochet, P.; Cadierno, V. Metal-Catalyzed Amide Bond Forming Reactions in an Environmentally Friendly Aqueous Medium: Nitrile Hydrations and Beyond Green Chem. 2013, 15 (1) 46-66 10.1039/C2GC36534K
    • (2013) Green Chem. , vol.15 , Issue.1 , pp. 46-66
    • García-Álvarez, R.1    Crochet, P.2    Cadierno, V.3
  • 42
    • 84876734216 scopus 로고    scopus 로고
    • Emerging Catalytic Methods for Amide Synthesis
    • Singh, C.; Kumar, V.; Sharma, U.; Kumar, N.; Singh, B. Emerging Catalytic Methods for Amide Synthesis Curr. Org. Synth. 2013, 10 (2) 241-264 10.2174/1570179411310020003
    • (2013) Curr. Org. Synth. , vol.10 , Issue.2 , pp. 241-264
    • Singh, C.1    Kumar, V.2    Sharma, U.3    Kumar, N.4    Singh, B.5
  • 44
    • 84922673500 scopus 로고    scopus 로고
    • Catalytic Synthesis of Amides via Aldoximes Rearrangement
    • Crochet, P.; Cadierno, V. Catalytic Synthesis of Amides via Aldoximes Rearrangement Chem. Commun. 2015, 51 (13) 2495-2505 10.1039/C4CC08684H
    • (2015) Chem. Commun. , vol.51 , Issue.13 , pp. 2495-2505
    • Crochet, P.1    Cadierno, V.2
  • 45
    • 54849440151 scopus 로고    scopus 로고
    • A Supported Rhodium Hydroxide Catalyst: Preparation, Characterization, and Scope of the Synthesis of Primary Amides from Aldoximes or Aldehydes
    • Fujiwara, H.; Ogasawara, Y.; Kotani, M.; Yamaguchi, K.; Mizuno, N. A Supported Rhodium Hydroxide Catalyst: Preparation, Characterization, and Scope of the Synthesis of Primary Amides from Aldoximes or Aldehydes Chem.-Asian J. 2008, 3 (8-9) 1715-1721 10.1002/asia.200800067
    • (2008) Chem. - Asian J. , vol.3 , Issue.8-9 , pp. 1715-1721
    • Fujiwara, H.1    Ogasawara, Y.2    Kotani, M.3    Yamaguchi, K.4    Mizuno, N.5
  • 47
    • 84882664897 scopus 로고    scopus 로고
    • Thiazolyl-Phosphine Hydrochloride Salts: Effective Auxiliary Ligands for Ruthenium-Catalyzed Nitrile Hydration Reactions and Related Amide Bond Forming Processes in Water
    • García-álvarez, R.; Zablocka, M.; Crochet, P.; Duhayon, C.; Majoral, J.-P.; Cadierno, V. Thiazolyl-Phosphine Hydrochloride Salts: Effective Auxiliary Ligands for Ruthenium-Catalyzed Nitrile Hydration Reactions and Related Amide Bond Forming Processes in Water Green Chem. 2013, 15 (9) 2447-2456 10.1039/c3gc41201f
    • (2013) Green Chem. , vol.15 , Issue.9 , pp. 2447-2456
    • García-Álvarez, R.1    Zablocka, M.2    Crochet, P.3    Duhayon, C.4    Majoral, J.-P.5    Cadierno, V.6
  • 48
    • 84877106928 scopus 로고    scopus 로고
    • Conversion of Aldoximes into Nitriles and Amides under Mild Conditions
    • Tambara, K.; Pantoş, G. D. Conversion of Aldoximes into Nitriles and Amides under Mild Conditions Org. Biomol. Chem. 2013, 11 (15) 2466-2472 10.1039/c3ob27362h
    • (2013) Org. Biomol. Chem. , vol.11 , Issue.15 , pp. 2466-2472
    • Tambara, K.1    Pantoş2    , G.D.3
  • 49
  • 50
    • 84935005612 scopus 로고    scopus 로고
    • Palladium(II) Complexes with a Phosphino-Oxime Ligand: Synthesis, Structure and Applications to the Catalytic Rearrangement and Dehydration of Aldoximes
    • Menéndez-Rodríguez, L.; Tomás-Mendivil, E.; Francos, J.; Nájera, C.; Crochet, P.; Cadierno, V. Palladium(II) Complexes with a Phosphino-Oxime Ligand: Synthesis, Structure and Applications to the Catalytic Rearrangement and Dehydration of Aldoximes Catal. Sci. Technol. 2015, 5 (7) 3754-3761 10.1039/C5CY00413F
    • (2015) Catal. Sci. Technol. , vol.5 , Issue.7 , pp. 3754-3761
    • Menéndez-Rodríguez, L.1    Tomás-Mendivil, E.2    Francos, J.3    Nájera, C.4    Crochet, P.5    Cadierno, V.6
  • 51
    • 34548529740 scopus 로고    scopus 로고
    • Highly Efficient Ruthenium-Catalyzed Oxime to Amide Rearrangement
    • Owston, N. A.; Parker, A. J.; Williams, J. M. J. Highly Efficient Ruthenium-Catalyzed Oxime to Amide Rearrangement Org. Lett. 2007, 9 (18) 3599-3601 10.1021/ol701445n
    • (2007) Org. Lett. , vol.9 , Issue.18 , pp. 3599-3601
    • Owston, N.A.1    Parker, A.J.2    Williams, J.M.J.3
  • 52
    • 68949163947 scopus 로고    scopus 로고
    • Significant Self-Acceleration Effects of Nitrile Additives in the Rhodium-Catalyzed Conversion of Aldoximes to Amides: A New Mechanistic Aspect
    • Kim, M.; Lee, J.; Lee, H.-Y.; Chang, S. Significant Self-Acceleration Effects of Nitrile Additives in the Rhodium-Catalyzed Conversion of Aldoximes to Amides: A New Mechanistic Aspect Adv. Synth. Catal. 2009, 351 (11-12) 1807-1812 10.1002/adsc.200900251
    • (2009) Adv. Synth. Catal. , vol.351 , Issue.11-12 , pp. 1807-1812
    • Kim, M.1    Lee, J.2    Lee, H.-Y.3    Chang, S.4
  • 53
    • 78649966271 scopus 로고    scopus 로고
    • Development of Versatile and Silver-Free Protocols for Gold(I) Catalysis
    • Gaillard, S.; Bosson, J.; Ramón, R. S.; Nun, P.; Slawin, A. M. Z.; Nolan, S. P. Development of Versatile and Silver-Free Protocols for Gold(I) Catalysis Chem.-Eur. J. 2010, 16 (46) 13729-13740 10.1002/chem.201001688
    • (2010) Chem. - Eur. J. , vol.16 , Issue.46 , pp. 13729-13740
    • Gaillard, S.1    Bosson, J.2    Ramón, R.S.3    Nun, P.4    Slawin, A.M.Z.5    Nolan, S.P.6
  • 54
    • 84255205689 scopus 로고    scopus 로고
    • Mechanistic Studies into Metal-Catalyzed Aldoxime to Amide Rearrangements
    • Allen, C. L.; Lawrence, R.; Emmett, L.; Williams, J. M. J. Mechanistic Studies into Metal-Catalyzed Aldoxime to Amide Rearrangements Adv. Synth. Catal. 2011, 353 (18) 3262-3268 10.1002/adsc.201100650
    • (2011) Adv. Synth. Catal. , vol.353 , Issue.18 , pp. 3262-3268
    • Allen, C.L.1    Lawrence, R.2    Emmett, L.3    Williams, J.M.J.4


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