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Volumn 7, Issue 6, 2015, Pages 477-482

Orthogonal tandem catalysis

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EID: 84930203318     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.2262     Document Type: Article
Times cited : (350)

References (55)
  • 2
    • 84898070874 scopus 로고    scopus 로고
    • Heterometallic complexes, tandem catalysis and catalytic cooperativity
    • Mata, J. A., Hahn, F. E. & Peris, E. Heterometallic complexes, tandem catalysis and catalytic cooperativity. Chem. Sci. 5, 1723-1732 (2014).
    • (2014) Chem. Sci. , vol.5 , pp. 1723-1732
    • Mata, J.A.1    Hahn, F.E.2    Peris, E.3
  • 3
    • 84887980354 scopus 로고    scopus 로고
    • Tandem catalysis: A new approach to polymers
    • Robert, C. & Tomas, C. M. Tandem catalysis: a new approach to polymers. Chem. Soc. Rev. 42, 9392-9402 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 9392-9402
    • Robert, C.1    Tomas, C.M.2
  • 5
    • 84859359524 scopus 로고    scopus 로고
    • Homogeneous and heterogeneous catalysts for multicomponent reactions
    • Climent, M. J., Corma, A. & Iborra, S. Homogeneous and heterogeneous catalysts for multicomponent reactions. R. Soc. Chem. Adv. 2, 16-58 (2012).
    • (2012) R. Soc. Chem. Adv. , vol.2 , pp. 16-58
    • Climent, M.J.1    Corma, A.2    Iborra, S.3
  • 6
    • 77749268378 scopus 로고    scopus 로고
    • Recent advances in multicatalyst promoted asymmetric tandem reactions
    • Zhou, J. Recent advances in multicatalyst promoted asymmetric tandem reactions. Chem. Asian J. 5, 422-434 (2010).
    • (2010) Chem. Asian J. , vol.5 , pp. 422-434
    • Zhou, J.1
  • 7
    • 84866425484 scopus 로고    scopus 로고
    • Etheric C-O bond hydrogenolysis using a tandem lanthanide trifate/supported palladium nanoparticle catalyst system
    • Atesin, A. C., Ray, N. A., Stair, P. C. & Marks, T. J. Etheric C-O bond hydrogenolysis using a tandem lanthanide trifate/supported palladium nanoparticle catalyst system. J. Am. Chem. Soc. 134, 14682-14685 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14682-14685
    • Atesin, A.C.1    Ray, N.A.2    Stair, P.C.3    Marks, T.J.4
  • 8
    • 84892184290 scopus 로고    scopus 로고
    • Rapid ether and alcohol C-O bond hydrogenolysis catalyzed by tandem high-valent metal trifate plus supported Pd catalysts
    • Li, Z., Assary, R. S., Atesin, A. C., Curtiss, L. A. & Marks, T. J. Rapid ether and alcohol C-O bond hydrogenolysis catalyzed by tandem high-valent metal trifate plus supported Pd catalysts. J. Am. Chem. Soc. 136, 104-107 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 104-107
    • Li, Z.1    Assary, R.S.2    Atesin, A.C.3    Curtiss, L.A.4    Marks, T.J.5
  • 9
    • 84885969523 scopus 로고    scopus 로고
    • A route for lignin and bio-oil conversion: Dehydroxylation of phenols into arenes by catalytic tandem reactions
    • Wang, X. & Rinaldi, R. A route for lignin and bio-oil conversion: dehydroxylation of phenols into arenes by catalytic tandem reactions. Ang e w. Chem. Int. Ed. 52, 11499-11503 (2013).
    • (2013) Ang e W. Chem. Int. Ed. , vol.52 , pp. 11499-11503
    • Wang, X.1    Rinaldi, R.2
  • 10
    • 84893853683 scopus 로고    scopus 로고
    • One-pot asymmetric nitro-mannich/hydroamination cascades for the synthesis of pyrrolidine derivatives: Combining organocatalysis and gold catalysis
    • Barber, D. M., ɰuriš, A., Tompson, A. L., Sanganee, H. J. & Dixon, D. J. One-pot asymmetric nitro-mannich/hydroamination cascades for the synthesis of pyrrolidine derivatives: combining organocatalysis and gold catalysis. ACS Catal. 4, 634-638 (2014).
    • (2014) ACS Catal. , vol.4 , pp. 634-638
    • Barber, D.M.1    ɰuriš, A.2    Tompson, A.L.3    Sanganee, H.J.4    Dixon, D.J.5
  • 11
    • 84890386396 scopus 로고    scopus 로고
    • Selective isomerization-hydroformylation sequence: A strategy to valuable α-methyl-branched aldehydes from terminal olefns
    • Dydio, P., Ploeger, M. & Reek, J. N. H. Selective isomerization-hydroformylation sequence: a strategy to valuable α-methyl-branched aldehydes from terminal olefns. ACS Catal. 3, 2939-2942 (2013).
    • (2013) ACS Catal. , vol.3 , pp. 2939-2942
    • Dydio, P.1    Ploeger, M.2    Reek, J.N.H.3
  • 12
    • 9744257740 scopus 로고    scopus 로고
    • Tandem catalysis: A taxonomy and illustrative review
    • Fogg, D. E. & dos Santos, E. N. Tandem catalysis: a taxonomy and illustrative review. Coord. Chem. Rev. 248, 2365-2379 (2004).
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 2365-2379
    • Fogg, D.E.1    Dos Santos, E.N.2
  • 13
    • 0037193122 scopus 로고    scopus 로고
    • In situ tandem allylic acetate isomerisation-ring closing metathesis: 1, 3-dimesityl-4, 5-dihydroimidazol-2-ylidene ruthenium benzylidenes and palladium(0)-phosphine combinations
    • Braddock, D. C. & Matsuno, A. In situ tandem allylic acetate isomerisation-ring closing metathesis: 1, 3-dimesityl-4, 5-dihydroimidazol-2-ylidene ruthenium benzylidenes and palladium(0)-phosphine combinations. Tetrahed. Lett. 43, 3305-3308 (2002).
    • (2002) Tetrahed. Lett. , vol.43 , pp. 3305-3308
    • Braddock, D.C.1    Matsuno, A.2
  • 14
    • 84896763365 scopus 로고    scopus 로고
    • Convergent catalysis: Asymmetric synthesis of dihydroquinolines using a combined metal catalysis and organocatalysis approach
    • Rueping, M., Dufour, J. & Bui, L. Convergent catalysis: asymmetric synthesis of dihydroquinolines using a combined metal catalysis and organocatalysis approach. ACS Catal. 4, 1021-1025 (2014).
    • (2014) ACS Catal. , vol.4 , pp. 1021-1025
    • Rueping, M.1    Dufour, J.2    Bui, L.3
  • 15
    • 84904290193 scopus 로고    scopus 로고
    • Scope and mechanism of homogeneous tantalum/iridium tandem catalytic alkane/alkene upgrading using sacrifcial hydrogen acceptors
    • Leitch, D. C., Labinger, J. A. & Bercaw, J. E. Scope and mechanism of homogeneous tantalum/iridium tandem catalytic alkane/alkene upgrading using sacrifcial hydrogen acceptors. Organometallics 33, 3353-3365 (2014).
    • (2014) Organometallics , vol.33 , pp. 3353-3365
    • Leitch, D.C.1    Labinger, J.A.2    Bercaw, J.E.3
  • 16
    • 84888388178 scopus 로고    scopus 로고
    • Tandem isomerization/hydroformylation/hydrogenation of internal alkenes to n-alcohols using Rh/Ru dual-or ternary-catalyst systems
    • Yuki, Y., Takahashi, K., Tanaka, Y. & Nozaki, K. Tandem isomerization/hydroformylation/hydrogenation of internal alkenes to n-alcohols using Rh/Ru dual-or ternary-catalyst systems. J. Am. Chem. Soc. 135, 17393-17400 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 17393-17400
    • Yuki, Y.1    Takahashi, K.2    Tanaka, Y.3    Nozaki, K.4
  • 17
    • 84880395587 scopus 로고    scopus 로고
    • Upgrading light hydrocarbons via tandem catalysis: A dual homogeneous Ta/Ir system for alkane/alkene coupling
    • Leitch, D. C., Lam, Y. C., Labinger, J. A. & Bercaw, J. E. Upgrading light hydrocarbons via tandem catalysis: a dual homogeneous Ta/Ir system for alkane/alkene coupling. J. Am. Chem. Soc. 135, 10302-10305 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 10302-10305
    • Leitch, D.C.1    Lam, Y.C.2    Labinger, J.A.3    Bercaw, J.E.4
  • 18
    • 84883889766 scopus 로고    scopus 로고
    • Reaction pathways and energetics of etheric C-O bond cleavage catalyzed by lanthanide trifates
    • Assary, R. S., Atesin, A. C., Li, Z., Curtiss, L. A. & Marks, T. J. Reaction pathways and energetics of etheric C-O bond cleavage catalyzed by lanthanide trifates. ACS Catal. 3, 1908-1914 (2013).
    • (2013) ACS Catal. , vol.3 , pp. 1908-1914
    • Assary, R.S.1    Atesin, A.C.2    Li, Z.3    Curtiss, L.A.4    Marks, T.J.5
  • 19
    • 84863430547 scopus 로고    scopus 로고
    • Alkane metathesis by tandem alkane-dehydrogenation-olefn-metathesis catalysis and related chemistry
    • Haibach, M. C., Kundu, S., Brookhart, M. & Goldman, A. S. Alkane metathesis by tandem alkane-dehydrogenation-olefn-metathesis catalysis and related chemistry. Acc. Chem. Res. 45, 947-958 (2012).
    • (2012) Acc. Chem. Res. , vol.45 , pp. 947-958
    • Haibach, M.C.1    Kundu, S.2    Brookhart, M.3    Goldman, A.S.4
  • 20
    • 84867489018 scopus 로고    scopus 로고
    • Acid-base bi-functionalized, large-pored mesoporous silica nanoparticles for cooperative catalysis of one-pot cellulose-to-HMF conversion
    • Peng, W-H., Lee, Y-Y., Wu, C. & Wu, K. C. W. Acid-base bi-functionalized, large-pored mesoporous silica nanoparticles for cooperative catalysis of one-pot cellulose-to-HMF conversion. J. Mater. Chem. 22, 23181-23185 (2012).
    • (2012) J. Mater. Chem. , vol.22 , pp. 23181-23185
    • Peng, W.-H.1    Lee, Y.-Y.2    Wu, C.3    Wu, K.C.W.4
  • 21
    • 84906250041 scopus 로고    scopus 로고
    • Multinuclear group 4 catalysis: Olefn polymerization pathways modifed by strong metal-metal cooperative efects
    • McInnis, J. P., Delferro, M. & Marks, T. J. Multinuclear group 4 catalysis: olefn polymerization pathways modifed by strong metal-metal cooperative efects. Acc. Chem. Res. 47, 2545-2557 (2014).
    • (2014) Acc. Chem. Res. , vol.47 , pp. 2545-2557
    • McInnis, J.P.1    Delferro, M.2    Marks, T.J.3
  • 22
    • 79952673359 scopus 로고    scopus 로고
    • Multinuclear olefn polymerization catalysts
    • Delferro, M. & Marks, T. J. Multinuclear olefn polymerization catalysts. Chem. Rev. 111, 2450-2485 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 2450-2485
    • Delferro, M.1    Marks, T.J.2
  • 23
    • 84893865666 scopus 로고    scopus 로고
    • Mechanistic studies of gold and palladium cooperative dual-catalytic cross-coupling systems
    • Al-Amin, M., Roth, K. E. & Blum, S. A. Mechanistic studies of gold and palladium cooperative dual-catalytic cross-coupling systems. ACS Catal. 4, 622-629 (2013).
    • (2013) ACS Catal. , vol.4 , pp. 622-629
    • Al-Amin, M.1    Roth, K.E.2    Blum, S.A.3
  • 24
    • 84887175689 scopus 로고    scopus 로고
    • Expanding the scope of metathesis: A survey of polyfunctional, single-site supported tungsten systems for hydrocarbon valorization
    • Popof, N., Mazoyer, E., Pelletier, J., Gauvin, R. M. & Taoufk, M. Expanding the scope of metathesis: a survey of polyfunctional, single-site supported tungsten systems for hydrocarbon valorization. Chem. Soc. Rev. 42, 9035-9054 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 9035-9054
    • Popof, N.1    Mazoyer, E.2    Pelletier, J.3    Gauvin, R.M.4    Taoufk, M.5
  • 26
    • 84876542084 scopus 로고    scopus 로고
    • Molecular redistribution and molecular averaging: Disproportionation of parafns via bifunctional catalysis
    • Chen, C. Y., O'Rear, D. J. & Leung, P. Molecular redistribution and molecular averaging: disproportionation of parafns via bifunctional catalysis. Top. Catal. 55, 1344-1361 (2012).
    • (2012) Top. Catal. , vol.55 , pp. 1344-1361
    • Chen, C.Y.1    O'Rear, D.J.2    Leung, P.3
  • 27
    • 84865130989 scopus 로고    scopus 로고
    • Olefn isomerization by iridium pincer catalysts. Experimental evidence for an eta(3)-allyl pathway and an unconventional mechanism predicted by DFT calculations
    • Biswas, S. et al. Olefn isomerization by iridium pincer catalysts. experimental evidence for an eta(3)-allyl pathway and an unconventional mechanism predicted by DFT calculations. J. Am. Chem. Soc. 134, 13276-13295 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13276-13295
    • Biswas, S.1
  • 28
    • 0037174388 scopus 로고    scopus 로고
    • On the mechanism of (PCP)Ir-catalyzed acceptorless dehydrogenation of alkanes: A combined computational and experimental study
    • Krogh-Jespersen, K. et al. On the mechanism of (PCP)Ir-catalyzed acceptorless dehydrogenation of alkanes: A combined computational and experimental study. J. Am. Chem. Soc. 124, 11404-11416 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11404-11416
    • Krogh-Jespersen, K.1
  • 30
    • 58549092048 scopus 로고    scopus 로고
    • Highly active and recyclable heterogeneous iridium pincer catalysts for transfer dehydrogenation of alkanes
    • Huang, Z. et al. Highly active and recyclable heterogeneous iridium pincer catalysts for transfer dehydrogenation of alkanes. Adv. Synth. Catal. 351, 188-206 (2009).
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 188-206
    • Huang, Z.1
  • 32
    • 0000322995 scopus 로고
    • Selective dimerization of monosubstituted alpha-olefns by tantalacyclopentane catalysts
    • Mclain, S. J., Sancho, J. & Schrock, R. R. Selective dimerization of monosubstituted alpha-olefns by tantalacyclopentane catalysts. J. Am. Chem. Soc. 102, 5610-5618 (1980).
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5610-5618
    • McLain, S.J.1    Sancho, J.2    Schrock, R.R.3
  • 33
    • 0000371480 scopus 로고
    • Synthesis of monomeric niobium-benzyne and tantalum-benzyne benzyne complexes and the molecular-structure of Ta(Eta-5-C5Me5)(C6H4)Me2
    • Mclain, S. J., Schrock, R. R., Sharp, P. R., Churchill, M. R. & Youngs, W. J. Synthesis of monomeric niobium-benzyne and tantalum-benzyne benzyne complexes and the molecular-structure of Ta(Eta-5-C5Me5)(C6H4)Me2. J. Am. Chem. Soc. 101, 263-265 (1979).
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 263-265
    • McLain, S.J.1    Schrock, R.R.2    Sharp, P.R.3    Churchill, M.R.4    Youngs, W.J.5
  • 34
    • 0001462275 scopus 로고
    • Metallacyclopentane to metallacyclobutane ring contraction
    • Mclain, S. J., Sancho, J. & Schrock, R. R. Metallacyclopentane to metallacyclobutane ring contraction. J. Am. Chem. Soc. 101, 5451-5453 (1979).
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 5451-5453
    • McLain, S.J.1    Sancho, J.2    Schrock, R.R.3
  • 35
    • 33645809744 scopus 로고    scopus 로고
    • Catalytic alkane metathesis by tandem alkane dehydrogenation olefn metathesis
    • Goldman, A. S. et al. Catalytic alkane metathesis by tandem alkane dehydrogenation olefn metathesis. Science 312, 257-261 (2006).
    • (2006) Science , vol.312 , pp. 257-261
    • Goldman, A.S.1
  • 36
    • 79952638279 scopus 로고    scopus 로고
    • Dehydrogenation and related reactions catalyzed by iridium pincer complexes
    • Choi, J., MacArthur, A. H., Brookhart, M. & Goldman, A. S. Dehydrogenation and related reactions catalyzed by iridium pincer complexes. Chem. Rev. 111, 1761-1779 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 1761-1779
    • Choi, J.1    MacArthur, A.H.2    Brookhart, M.3    Goldman, A.S.4
  • 37
    • 84865405024 scopus 로고    scopus 로고
    • Isomerizing olefn metathesis as a strategy to access defned distributions of unsaturated compounds from fatty acids
    • Ohlmann, D. M. et al. Isomerizing olefn metathesis as a strategy to access defned distributions of unsaturated compounds from fatty acids. J. Am. Chem. Soc. 134, 13716-13729 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13716-13729
    • Ohlmann, D.M.1
  • 39
    • 84887904714 scopus 로고    scopus 로고
    • Oligomerization of ethylene to alpha-olefns: Discovery and development of the shell higher olefn process (SHOP)
    • Keim, W. Oligomerization of ethylene to alpha-olefns: discovery and development of the shell higher olefn process (SHOP). Angew. Chem. Int. Ed. 52, 12492-12496 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 12492-12496
    • Keim, W.1
  • 40
    • 80755126268 scopus 로고    scopus 로고
    • Cascade catalysis for the homogeneous hydrogenation of CO2 to Methanol
    • Huf, C. A. & Sanford, M. S. Cascade catalysis for the homogeneous hydrogenation of CO2 to Methanol. J. Am. Chem. Soc. 133, 18122-18125 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 18122-18125
    • Huf, C.A.1    Sanford, M.S.2
  • 41
    • 84903795111 scopus 로고    scopus 로고
    • Tandem catalytic conversion of glucose to 5-hydroxymethylfurfural with an immobilized enzyme and a solid acid
    • Huang, H. et al. Tandem catalytic conversion of glucose to 5-hydroxymethylfurfural with an immobilized enzyme and a solid acid. ACS Catal. 4, 2165-2168 (2014).
    • (2014) ACS Catal. , vol.4 , pp. 2165-2168
    • Huang, H.1
  • 42
    • 54749101112 scopus 로고    scopus 로고
    • Direct, high-yield conversion of cellulose into biofuel
    • Mascal, M. & Nikitin, E. B. Direct, high-yield conversion of cellulose into biofuel. Angew. Chem. Int. Ed. 47, 7924-7926 (2008).
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7924-7926
    • Mascal, M.1    Nikitin, E.B.2
  • 43
    • 76249123783 scopus 로고    scopus 로고
    • Integrating enzymatic and acid catalysis to convert glucose into 5-hydroxymethylfurfural
    • Huang, R. L., Qi, W., Su, R. X. & He, Z. M. Integrating enzymatic and acid catalysis to convert glucose into 5-hydroxymethylfurfural. Chem. Commun. 46, 1115-1117 (2010).
    • (2010) Chem. Commun. , vol.46 , pp. 1115-1117
    • Huang, R.L.1    Qi, W.2    Su, R.X.3    He, Z.M.4
  • 44
    • 84867578933 scopus 로고    scopus 로고
    • Mechanism of Bronsted acid-catalyzed conversion of carbohydrates
    • Yang, G., Pidko, E. A. & Hensen, E. J. M. Mechanism of Bronsted acid-catalyzed conversion of carbohydrates. J. Catal. 295, 122-132 (2012).
    • (2012) J. Catal. , vol.295 , pp. 122-132
    • Yang, G.1    Pidko, E.A.2    Hensen, E.J.M.3
  • 45
    • 84878622602 scopus 로고    scopus 로고
    • Integrated chemo-enzymatic production of 5-hydroxymethylfurfural from glucose
    • Simeonov, S. P., Coelho, J. A. S. & Afonso, C. A. M. Integrated chemo-enzymatic production of 5-hydroxymethylfurfural from glucose. ChemSusChem 6, 997-1000 (2013).
    • (2013) ChemSusChem , vol.6 , pp. 997-1000
    • Simeonov, S.P.1    Coelho, J.A.S.2    Afonso, C.A.M.3
  • 46
    • 84863713762 scopus 로고    scopus 로고
    • Chemo-enzymatic conversion of glucose into 5-hydroxymethylfurfural in seawater
    • Grande, P. M., Bergs, C. & de Maria, P. D. Chemo-enzymatic conversion of glucose into 5-hydroxymethylfurfural in seawater. ChemSusChem 5, 1203-1206 (2012).
    • (2012) ChemSusChem , vol.5 , pp. 1203-1206
    • Grande, P.M.1    Bergs, C.2    De Maria, P.D.3
  • 47
    • 21044443212 scopus 로고    scopus 로고
    • Combined ruthenium(ii) and lipase catalysis for efcient dynamic kinetic resolution of secondary alcohols. Insight into the racemization mechanism
    • Martin-Matute, B., Edin, M., Bogar, K., Kaynak, F. B. & Bäckvall, J. E. Combined ruthenium(ii) and lipase catalysis for efcient dynamic kinetic resolution of secondary alcohols. Insight into the racemization mechanism. J. Am. Chem. Soc. 127, 8817-8825 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 8817-8825
    • Martin-Matute, B.1    Edin, M.2    Bogar, K.3    Kaynak, F.B.4    Bäckvall, J.E.5
  • 48
    • 11144319821 scopus 로고    scopus 로고
    • Highly compatible metal and enzyme catalysts for efcient dynamic kinetic resolution of alcohols at ambient temperature
    • Martin-Matute, B., Edin, M., Bogar, K. & Bäckvall, J. E. Highly compatible metal and enzyme catalysts for efcient dynamic kinetic resolution of alcohols at ambient temperature. Angew. Chem. Int. Ed. 43, 6535-6539 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 6535-6539
    • Martin-Matute, B.1    Edin, M.2    Bogar, K.3    Bäckvall, J.E.4
  • 49
    • 80052834742 scopus 로고    scopus 로고
    • Domino rhodium-catalyzed alkyne arylation/palladium-catalyzed N arylation: A mechanistic investigation
    • Panteleev, J., Zhang, L. & Lautens, M. Domino rhodium-catalyzed alkyne arylation/palladium-catalyzed N arylation: a mechanistic investigation. Angew. Chem. Int. Ed. 50, 9089-9092 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9089-9092
    • Panteleev, J.1    Zhang, L.2    Lautens, M.3
  • 50
    • 84883527198 scopus 로고    scopus 로고
    • Rh/Pd catalysis with chiral and achiral ligands: Domino synthesis of aza-dihydrodibenzoxepines
    • Friedman, A. A., Panteleev, J., Tsoung, J., Huynh, V. & Lautens, M. Rh/Pd catalysis with chiral and achiral ligands: domino synthesis of aza-dihydrodibenzoxepines. Angew. Chem. Int. Ed. 52, 9755-9758 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9755-9758
    • Friedman, A.A.1    Panteleev, J.2    Tsoung, J.3    Huynh, V.4    Lautens, M.5
  • 51
    • 62649160608 scopus 로고    scopus 로고
    • Intramolecular hydroalkoxylation/cyclization of alkynyl alcohols mediated by lanthanide catalysts. Scope and reaction mechanism
    • Seo, S. Y., Yu, X. H. & Marks, T. J. Intramolecular hydroalkoxylation/cyclization of alkynyl alcohols mediated by lanthanide catalysts. scope and reaction mechanism. J. Am. Chem. Soc. 131, 263-276 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 263-276
    • Seo, S.Y.1    Yu, X.H.2    Marks, T.J.3
  • 52
    • 77949291993 scopus 로고    scopus 로고
    • Efcient intramolecular hydroalkoxylation of unactivated alkenols mediated by recyclable lanthanide trifate ionic liquids: Scope and mechanism
    • Dzudza, A. & Marks, T. J. Efcient intramolecular hydroalkoxylation of unactivated alkenols mediated by recyclable lanthanide trifate ionic liquids: scope and mechanism. Chem. Eur. J. 16, 3403-3422 (2010).
    • (2010) Chem. Eur. J. , vol.16 , pp. 3403-3422
    • Dzudza, A.1    Marks, T.J.2
  • 53
    • 64349115503 scopus 로고    scopus 로고
    • Efcient intramolecular hydroalkoxylation/cyclization of unactivated alkenols mediated by lanthanide trifate ionic liquids
    • Dzudza, A. & Marks, T. J. Efcient intramolecular hydroalkoxylation/cyclization of unactivated alkenols mediated by lanthanide trifate ionic liquids. Org. Lett. 11, 1523-1526 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 1523-1526
    • Dzudza, A.1    Marks, T.J.2
  • 54
    • 84876854416 scopus 로고    scopus 로고
    • The hydrodeoxygenation of bioderived furans into alkanes
    • Sutton, A. D. et al. The hydrodeoxygenation of bioderived furans into alkanes. Nature Chem. 5, 428-432 (2013).
    • (2013) Nature Chem. , vol.5 , pp. 428-432
    • Sutton, A.D.1
  • 55
    • 84890374848 scopus 로고    scopus 로고
    • Integration of chemical and biological catalysis: Production of furylglycolic acid from glucose via cortalcerone
    • Schwartz, T. J. et al. Integration of chemical and biological catalysis: production of furylglycolic acid from glucose via cortalcerone. ACS Catal. 3, 2689-2693 (2013).
    • (2013) ACS Catal. , vol.3 , pp. 2689-2693
    • Schwartz, T.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.