메뉴 건너뛰기




Volumn 49, Issue 4, 2016, Pages 594-605

The Development and Application of Two-Chamber Reactors and Carbon Monoxide Precursors for Safe Carbonylation Reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84966267415     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.5b00471     Document Type: Article
Times cited : (387)

References (48)
  • 1
    • 8444233969 scopus 로고    scopus 로고
    • Evolution of carbonylation catalysis: No need for carbon monoxide
    • Morimoto, T.; Kakiuchi, K. Evolution of carbonylation catalysis: No need for carbon monoxide Angew. Chem., Int. Ed. 2004, 43, 5580-5588 10.1002/anie.200301736
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5580-5588
    • Morimoto, T.1    Kakiuchi, K.2
  • 2
    • 84942108165 scopus 로고    scopus 로고
    • Recent advances in the transition metal catalyzed carbonylation of alkynes, arenes and aryl halides using CO surrogates
    • references therein
    • Gautam, P.; Bhanage, B. M. Recent advances in the transition metal catalyzed carbonylation of alkynes, arenes and aryl halides using CO surrogates Catal. Sci. Technol. 2015, 5, 4663-4702 and references therein. 10.1039/C5CY00691K
    • (2015) Catal. Sci. Technol. , vol.5 , pp. 4663-4702
    • Gautam, P.1    Bhanage, B.M.2
  • 3
    • 77957148417 scopus 로고    scopus 로고
    • Molybdenum-Mediated Carbonylation of Aryl Halides with Nucleophiles Using Microwave Irradiation
    • Roberts, B.; Liptrot, D.; Alcaraz, L.; Luker, T.; Stocks, M. Molybdenum-Mediated Carbonylation of Aryl Halides with Nucleophiles Using Microwave Irradiation Org. Lett. 2010, 12, 4280-4283 10.1021/ol1016965
    • (2010) Org. Lett. , vol.12 , pp. 4280-4283
    • Roberts, B.1    Liptrot, D.2    Alcaraz, L.3    Luker, T.4    Stocks, M.5
  • 4
    • 80755123259 scopus 로고    scopus 로고
    • Silacarboxylic Acids as Efficient Carbon Monoxide Releasing Molecules: Synthesis and Application in Palladium-Catalyzed Carbonylation Reactions
    • Friis, S. D.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. Silacarboxylic Acids as Efficient Carbon Monoxide Releasing Molecules: Synthesis and Application in Palladium-Catalyzed Carbonylation Reactions J. Am. Chem. Soc. 2011, 133, 18114-18117 10.1021/ja208652n
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 18114-18117
    • Friis, S.D.1    Taaning, R.H.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 6
    • 84862562423 scopus 로고    scopus 로고
    • Isotope-Labeling of the Fibril Binding Compound FSB via a Pd-Catalyzed Double Alkoxycarbonylation
    • Burhardt, M. N.; Taaning, R.; Nielsen, N. C.; Skrydstrup, T. Isotope-Labeling of the Fibril Binding Compound FSB via a Pd-Catalyzed Double Alkoxycarbonylation J. Org. Chem. 2012, 77, 5357-5363 10.1021/jo300746x
    • (2012) J. Org. Chem. , vol.77 , pp. 5357-5363
    • Burhardt, M.N.1    Taaning, R.2    Nielsen, N.C.3    Skrydstrup, T.4
  • 8
    • 84872246718 scopus 로고    scopus 로고
    • Synthesis of Heterocycles via Palladium-Catalyzed Carbonylations
    • Wu, X.-F.; Neumann, H.; Beller, M. Synthesis of Heterocycles via Palladium-Catalyzed Carbonylations Chem. Rev. 2013, 113, 1-35 10.1021/cr300100s
    • (2013) Chem. Rev. , vol.113 , pp. 1-35
    • Wu, X.-F.1    Neumann, H.2    Beller, M.3
  • 9
    • 80855133545 scopus 로고    scopus 로고
    • Oxidative Carbonylation Reactions: Organometallic Compounds (R-M) or Hydrocarbons (R-H) as Nucleophiles
    • Liu, Q.; Zhang, H.; Lei, A. Oxidative Carbonylation Reactions: Organometallic Compounds (R-M) or Hydrocarbons (R-H) as Nucleophiles Angew. Chem., Int. Ed. 2011, 50, 10788-10799 10.1002/anie.201100763
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 10788-10799
    • Liu, Q.1    Zhang, H.2    Lei, A.3
  • 10
    • 35048883596 scopus 로고    scopus 로고
    • Ed. Topics in Organometallic Chemistry; Springer
    • Catalytic Carbonylation Reactions; Beller, M., Ed.; Topics in Organometallic Chemistry; Springer, 2006; Vol. 18.
    • (2006) Catalytic Carbonylation Reactions , vol.18
    • Beller, M.1
  • 11
    • 84902258984 scopus 로고    scopus 로고
    • Carbonylations of Alkenes with CO Surrogates
    • Wu, L. P.; Liu, Q.; Jackstell, R.; Beller, M. Carbonylations of Alkenes with CO Surrogates Angew. Chem., Int. Ed. 2014, 53, 6310-6320 10.1002/anie.201400793
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 6310-6320
    • Wu, L.P.1    Liu, Q.2    Jackstell, R.3    Beller, M.4
  • 12
    • 0001420460 scopus 로고
    • Palladium-catalyzed amidation of aryl, heterocyclic, and vinylic halides
    • Schoenberg, A.; Heck, R. F. Palladium-catalyzed amidation of aryl, heterocyclic, and vinylic halides J. Org. Chem. 1974, 39, 3327-3331 10.1021/jo00937a004
    • (1974) J. Org. Chem. , vol.39 , pp. 3327-3331
    • Schoenberg, A.1    Heck, R.F.2
  • 13
    • 84871557158 scopus 로고    scopus 로고
    • 6 and a Bridged Two-Vial System: Allowing the Use of Nitro Group Substituted Aryl Iodides and Aryl Bromides
    • 6 and a Bridged Two-Vial System: Allowing the Use of Nitro Group Substituted Aryl Iodides and Aryl Bromides J. Org. Chem. 2012, 77, 11393-11398 10.1021/jo302322w
    • (2012) J. Org. Chem. , vol.77 , pp. 11393-11398
    • Nordeman, P.1    Odell, L.R.2    Larhed, M.3
  • 14
    • 84906281523 scopus 로고    scopus 로고
    • Mild Pd-Catalyzed Aminocarbonylation of (Hetero)Aryl Bromides with a Palladacycle Precatalyst
    • Friis, S. D.; Skrydstrup, T.; Buchwald, S. L. Mild Pd-Catalyzed Aminocarbonylation of (Hetero)Aryl Bromides with a Palladacycle Precatalyst Org. Lett. 2014, 16, 4296-4299 10.1021/ol502014b
    • (2014) Org. Lett. , vol.16 , pp. 4296-4299
    • Friis, S.D.1    Skrydstrup, T.2    Buchwald, S.L.3
  • 15
    • 33646898870 scopus 로고    scopus 로고
    • Remarkable ligand effect on the palladium-catalyzed double carbonylation of aryl iodides
    • Iizuka, M.; Kondo, Y. Remarkable ligand effect on the palladium-catalyzed double carbonylation of aryl iodides Chem. Commun. 2006, 1739-1741 10.1039/b600632a
    • (2006) Chem. Commun. , pp. 1739-1741
    • Iizuka, M.1    Kondo, Y.2
  • 17
    • 80051702318 scopus 로고    scopus 로고
    • Palladium-Catalyzed Approach to Primary Amides Using Nongaseous Precursors
    • Nielsen, D. U.; Taaning, R. H.; Lindhardt, A. T.; Gøgsig, T. M.; Skrydstrup, T. Palladium-Catalyzed Approach to Primary Amides Using Nongaseous Precursors Org. Lett. 2011, 13, 4454-4457 10.1021/ol201808y
    • (2011) Org. Lett. , vol.13 , pp. 4454-4457
    • Nielsen, D.U.1    Taaning, R.H.2    Lindhardt, A.T.3    Gøgsig, T.M.4    Skrydstrup, T.5
  • 18
    • 84941145428 scopus 로고    scopus 로고
    • 1,2,4- and 1,3,4-Oxadiazole Synthesis by Palladium-Catalyzed Carbonylative Assembly of Aryl Bromides with Amidoximes or Hydrazides
    • Andersen, T. L.; Caneschi, W.; Ayoub, A.; Lindhardt, A. T.; Couri, M. R. C.; Skrydstrup, T. 1,2,4- and 1,3,4-Oxadiazole Synthesis by Palladium-Catalyzed Carbonylative Assembly of Aryl Bromides with Amidoximes or Hydrazides Adv. Synth. Catal. 2014, 356, 3074-3082 10.1002/adsc.201400487
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 3074-3082
    • Andersen, T.L.1    Caneschi, W.2    Ayoub, A.3    Lindhardt, A.T.4    Couri, M.R.C.5    Skrydstrup, T.6
  • 19
    • 84901585800 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylation of Aryl Bromides with N-Substituted Cyanamides
    • Lian, Z.; Friis, S. D.; Lindhardt, A. T.; Skrydstrup, T. Palladium-Catalyzed Carbonylation of Aryl Bromides with N-Substituted Cyanamides Synlett 2014, 25, 1241-1245 10.1055/s-0033-1341200
    • (2014) Synlett , vol.25 , pp. 1241-1245
    • Lian, Z.1    Friis, S.D.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 20
    • 84924275665 scopus 로고    scopus 로고
    • Synthesis of Acyl Carbamates via Four Component Pd-Catalyzed Carbonylative Coupling of Aryl Halides, Potassium Cyanate, and Alcohols
    • reference 13a therein
    • Yin, H.; de Almeida, A. M.; de Almeida, M. V.; Lindhardt, A. T.; Skrydstrup, T. Synthesis of Acyl Carbamates via Four Component Pd-Catalyzed Carbonylative Coupling of Aryl Halides, Potassium Cyanate, and Alcohols Org. Lett. 2015, 17, 1248-1251 and reference 13a therein. 10.1021/acs.orglett.5b00221
    • (2015) Org. Lett. , vol.17 , pp. 1248-1251
    • Yin, H.1    De Almeida, A.M.2    De Almeida, M.V.3    Lindhardt, A.T.4    Skrydstrup, T.5
  • 21
    • 84855478761 scopus 로고    scopus 로고
    • An Efficient Method for the Preparation of Tertiary Esters by Palladium-Catalyzed Alkoxycarbonylation of Aryl Bromides
    • Xin, Z.; Gøgsig, T. M.; Lindhardt, A. T.; Skrydstrup, T. An Efficient Method for the Preparation of Tertiary Esters by Palladium-Catalyzed Alkoxycarbonylation of Aryl Bromides Org. Lett. 2012, 14, 284-287 10.1021/ol203057w
    • (2012) Org. Lett. , vol.14 , pp. 284-287
    • Xin, Z.1    Gøgsig, T.M.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 22
    • 84922727306 scopus 로고    scopus 로고
    • General Method for the Preparation of Active Esters by Palladium-Catalyzed Alkoxycarbonylation of Aryl Bromides
    • de Almeida, A. M.; Andersen, T. L.; Lindhardt, A. T.; de Almeida, M. V.; Skrydstrup, T. General Method for the Preparation of Active Esters by Palladium-Catalyzed Alkoxycarbonylation of Aryl Bromides J. Org. Chem. 2015, 80, 1920-1928 10.1021/jo5025464
    • (2015) J. Org. Chem. , vol.80 , pp. 1920-1928
    • De Almeida, A.M.1    Andersen, T.L.2    Lindhardt, A.T.3    De Almeida, M.V.4    Skrydstrup, T.5
  • 23
    • 43449133006 scopus 로고    scopus 로고
    • Palladium-Catalyzed Thiocarbonylation fo Iodoarenes with Thiols in Phosphonium Salt Ionic Liquids
    • Cao, H.; McNamee, L.; Alper, H. Palladium-Catalyzed Thiocarbonylation fo Iodoarenes with Thiols in Phosphonium Salt Ionic Liquids J. Org. Chem. 2008, 73, 3530-3534 10.1021/jo800287s
    • (2008) J. Org. Chem. , vol.73 , pp. 3530-3534
    • Cao, H.1    McNamee, L.2    Alper, H.3
  • 24
    • 84873948766 scopus 로고    scopus 로고
    • Pd-Catalyzed Thiocarbonylation with Stoichiometric Carbon Monoxide: Scope and Applications
    • Burhardt, M. N.; Taaning, R. H.; Skrydstrup, T. Pd-Catalyzed Thiocarbonylation with Stoichiometric Carbon Monoxide: Scope and Applications Org. Lett. 2013, 15, 948-951 10.1021/ol400138m
    • (2013) Org. Lett. , vol.15 , pp. 948-951
    • Burhardt, M.N.1    Taaning, R.H.2    Skrydstrup, T.3
  • 25
    • 84919687882 scopus 로고    scopus 로고
    • Palladium-catalyzed thiocarbonylation of aryl, vinyl, and benzyl bromides
    • Burhardt, M. N.; Ahlburg, A.; Skrydstrup, T. Palladium-catalyzed thiocarbonylation of aryl, vinyl, and benzyl bromides J. Org. Chem. 2014, 79, 11830-11840 10.1021/jo5009965
    • (2014) J. Org. Chem. , vol.79 , pp. 11830-11840
    • Burhardt, M.N.1    Ahlburg, A.2    Skrydstrup, T.3
  • 26
    • 0030664209 scopus 로고    scopus 로고
    • Palladium-catalyzed alpha-arylation of ketones
    • Palucki, M.; Buchwald, S. L. Palladium-catalyzed alpha-arylation of ketones J. Am. Chem. Soc. 1997, 119, 11108-11109 10.1021/ja972593s
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11108-11109
    • Palucki, M.1    Buchwald, S.L.2
  • 27
    • 0000014063 scopus 로고    scopus 로고
    • Palladium-catalyzed direct alpha-arylation of ketones. Rate acceleration by sterically hindered chelating ligands and reductive elimination from a transition metal enolate complex
    • Hamann, B. C.; Hartwig, J. F. Palladium-catalyzed direct alpha-arylation of ketones. Rate acceleration by sterically hindered chelating ligands and reductive elimination from a transition metal enolate complex J. Am. Chem. Soc. 1997, 119, 12382-12383 10.1021/ja9727880
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12382-12383
    • Hamann, B.C.1    Hartwig, J.F.2
  • 28
    • 84855812682 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylative α-Arylation for Accessing 1,3-Diketones
    • Gøgsig, T. M.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. Palladium-Catalyzed Carbonylative α-Arylation for Accessing 1,3-Diketones Angew. Chem., Int. Ed. 2012, 51, 798-801 10.1002/anie.201107494
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 798-801
    • Gøgsig, T.M.1    Taaning, R.H.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 29
    • 84891017201 scopus 로고    scopus 로고
    • Pd-Catalyzed Carbonylative alpha-Arylation of Aryl Bromides: Scope and Mechanistic Studies
    • Nielsen, D. U.; Lescot, C.; Gogsig, T. M.; Lindhardt, A. T.; Skrydstrup, T. Pd-Catalyzed Carbonylative alpha-Arylation of Aryl Bromides: Scope and Mechanistic Studies Chem.-Eur. J. 2013, 19, 17926-17938 10.1002/chem.201303384
    • (2013) Chem. - Eur. J. , vol.19 , pp. 17926-17938
    • Nielsen, D.U.1    Lescot, C.2    Gogsig, T.M.3    Lindhardt, A.T.4    Skrydstrup, T.5
  • 30
    • 84869994129 scopus 로고    scopus 로고
    • A Selective Palladium-Catalyzed Carbonylative Arylation of Aryl Ketones to Give Vinylbenzoate Compounds
    • Schranck, J.; Tlili, A.; Neumann, H.; Alsabeh, P. G.; Stradiotto, M.; Beller, M. A Selective Palladium-Catalyzed Carbonylative Arylation of Aryl Ketones to Give Vinylbenzoate Compounds Chem.-Eur. J. 2012, 18, 15592-15597 10.1002/chem.201202895
    • (2012) Chem. - Eur. J. , vol.18 , pp. 15592-15597
    • Schranck, J.1    Tlili, A.2    Neumann, H.3    Alsabeh, P.G.4    Stradiotto, M.5    Beller, M.6
  • 31
    • 84883519138 scopus 로고    scopus 로고
    • Access to β-Keto Esters by Palladium-Catalyzed Carbonylative Coupling of Aryl Halides with Monoester Potassium Malonates
    • Korsager, S.; Nielsen, D. U.; Taaning, R. H.; Skrydstrup, T. Access to β-Keto Esters by Palladium-Catalyzed Carbonylative Coupling of Aryl Halides with Monoester Potassium Malonates Angew. Chem., Int. Ed. 2013, 52, 9763-9766 10.1002/anie.201304072
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 9763-9766
    • Korsager, S.1    Nielsen, D.U.2    Taaning, R.H.3    Skrydstrup, T.4
  • 32
    • 84890984413 scopus 로고    scopus 로고
    • Direct Route to 1,3-Diketones by Palladium-Catalyzed Carbonylative Coupling of Aryl Halides with Acetylacetone
    • Korsager, S.; Nielsen, D. U.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. Direct Route to 1,3-Diketones by Palladium-Catalyzed Carbonylative Coupling of Aryl Halides with Acetylacetone Chem.-Eur. J. 2013, 19, 17687-17691 10.1002/chem.201303872
    • (2013) Chem. - Eur. J. , vol.19 , pp. 17687-17691
    • Korsager, S.1    Nielsen, D.U.2    Taaning, R.H.3    Lindhardt, A.T.4    Skrydstrup, T.5
  • 33
    • 84915748539 scopus 로고    scopus 로고
    • A Palladium-Catalyzed Carbonylative-Deacetylative Sequence to 1,3-Keto Amides
    • Nielsen, D. U.; Korsager, S.; Lindhardt, A. T.; Skrydstrup, T. A Palladium-Catalyzed Carbonylative-Deacetylative Sequence to 1,3-Keto Amides Adv. Synth. Catal. 2014, 356, 3519-3524 10.1002/adsc.201400545
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 3519-3524
    • Nielsen, D.U.1    Korsager, S.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 34
    • 84938507943 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylative Coupling of (2-Azaaryl)methyl Anion Equivalents with (Hetero)Aryl Bromides
    • Jusseau, X.; Yin, H.; Lindhardt, A. T.; Skrydstrup, T. Palladium-Catalyzed Carbonylative Coupling of (2-Azaaryl)methyl Anion Equivalents with (Hetero)Aryl Bromides Chem.-Eur. J. 2014, 20, 15785-15789 10.1002/chem.201404751
    • (2014) Chem. - Eur. J. , vol.20 , pp. 15785-15789
    • Jusseau, X.1    Yin, H.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 35
    • 84906949141 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylative alpha-Arylation of 2-Oxindoles with (Hetero) aryl Bromides: Efficient and Complementary Approach to 3-Acyl-2-oxindoles
    • Lian, Z.; Friis, S. D.; Skrydstrup, T. Palladium-Catalyzed Carbonylative alpha-Arylation of 2-Oxindoles with (Hetero) aryl Bromides: Efficient and Complementary Approach to 3-Acyl-2-oxindoles Angew. Chem., Int. Ed. 2014, 53, 9582-9586 10.1002/anie.201404217
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 9582-9586
    • Lian, Z.1    Friis, S.D.2    Skrydstrup, T.3
  • 36
    • 84923206722 scopus 로고    scopus 로고
    • Palladium-catalysed carbonylative alpha-arylation of nitromethane
    • Lian, Z.; Friis, S. D.; Skrydstrup, T. Palladium-catalysed carbonylative alpha-arylation of nitromethane Chem. Commun. 2015, 51, 3600-3603 10.1039/C5CC00123D
    • (2015) Chem. Commun. , vol.51 , pp. 3600-3603
    • Lian, Z.1    Friis, S.D.2    Skrydstrup, T.3
  • 38
    • 79955074018 scopus 로고    scopus 로고
    • The 2010 Nobel Prize in Chemistry: Palladium-Catalysed Cross-Coupling
    • Colacot, T. J. The 2010 Nobel Prize in Chemistry: Palladium-Catalysed Cross-Coupling Platinum Met. Rev. 2011, 55, 84-90 10.1595/147106711X558301
    • (2011) Platinum Met. Rev. , vol.55 , pp. 84-90
    • Colacot, T.J.1
  • 39
    • 84886392074 scopus 로고    scopus 로고
    • An Air-Tolerant Approach to the Carbonylative Suzuki-Miyaura Coupling: Applications in Isotope Labeling
    • Ahlburg, A.; Lindhardt, A. T.; Taaning, R. H.; Modvig, A. E.; Skrydstrup, T. An Air-Tolerant Approach to the Carbonylative Suzuki-Miyaura Coupling: Applications in Isotope Labeling J. Org. Chem. 2013, 78, 10310-10318 10.1021/jo401696c
    • (2013) J. Org. Chem. , vol.78 , pp. 10310-10318
    • Ahlburg, A.1    Lindhardt, A.T.2    Taaning, R.H.3    Modvig, A.E.4    Skrydstrup, T.5
  • 40
    • 84898714900 scopus 로고    scopus 로고
    • Carbonylative Suzuki Couplings of Aryl Bromides with Boronic Acid Derivatives under Base-Free Conditions
    • Bjerglund, K. M.; Skrydstrup, T.; Molander, G. A. Carbonylative Suzuki Couplings of Aryl Bromides with Boronic Acid Derivatives under Base-Free Conditions Org. Lett. 2014, 16, 1888-1891 10.1021/ol5003362
    • (2014) Org. Lett. , vol.16 , pp. 1888-1891
    • Bjerglund, K.M.1    Skrydstrup, T.2    Molander, G.A.3
  • 41
    • 0001120816 scopus 로고
    • Palladium-Catalyzed Cross-Carbonylation of Aryl Iodides with 5-Membered Cyclic Olefins
    • Satoh, T.; Itaya, T.; Okuro, K.; Miura, M.; Nomura, M. Palladium-Catalyzed Cross-Carbonylation of Aryl Iodides with 5-Membered Cyclic Olefins J. Org. Chem. 1995, 60, 7267-7271 10.1021/jo00127a035
    • (1995) J. Org. Chem. , vol.60 , pp. 7267-7271
    • Satoh, T.1    Itaya, T.2    Okuro, K.3    Miura, M.4    Nomura, M.5
  • 42
    • 79955588070 scopus 로고    scopus 로고
    • Carbonylative Heck Reactions Using CO Generated ex Situ in a Two-Chamber System
    • Hermange, P.; Gøgsig, T. M.; Lindhardt, A. T.; Taaning, R. H.; Skrydstrup, T. Carbonylative Heck Reactions Using CO Generated ex Situ in a Two-Chamber System Org. Lett. 2011, 13, 2444-2447 10.1021/ol200686h
    • (2011) Org. Lett. , vol.13 , pp. 2444-2447
    • Hermange, P.1    Gøgsig, T.M.2    Lindhardt, A.T.3    Taaning, R.H.4    Skrydstrup, T.5
  • 43
    • 84862085549 scopus 로고    scopus 로고
    • Palladium Catalyzed Carbonylative Heck Reaction Affording Monoprotected 1,3-Ketoaldehydes
    • Gogsig, T. M.; Nielsen, D. U.; Lindhardt, A. T.; Skrydstrup, T. Palladium Catalyzed Carbonylative Heck Reaction Affording Monoprotected 1,3-Ketoaldehydes Org. Lett. 2012, 14, 2536-2539 10.1021/ol300837d
    • (2012) Org. Lett. , vol.14 , pp. 2536-2539
    • Gogsig, T.M.1    Nielsen, D.U.2    Lindhardt, A.T.3    Skrydstrup, T.4
  • 44
    • 37049100346 scopus 로고
    • Carbonylation of organic halides in the presence of terminal acetylenes; Novel acetylenic ketone synthesis J. Chem. Soc
    • Kobayashi, T.; Tanaka, M. Carbonylation of organic halides in the presence of terminal acetylenes; novel acetylenic ketone synthesis J. Chem. Soc J. Chem. Soc., Chem. Commun. 1981, 333-334 10.1039/c39810000333
    • (1981) J. Chem. Soc., Chem. Commun. , pp. 333-334
    • Kobayashi, T.1    Tanaka, M.2
  • 45
    • 84898968032 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Bromides Using Near Stoichiometric Carbon Monoxide
    • Neumann, K. T.; Laursen, S. R.; Lindhardt, A. T.; Bang-Andersen, B.; Skrydstrup, T. Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Bromides Using Near Stoichiometric Carbon Monoxide Org. Lett. 2014, 16, 2216-2219 10.1021/ol5007289
    • (2014) Org. Lett. , vol.16 , pp. 2216-2219
    • Neumann, K.T.1    Laursen, S.R.2    Lindhardt, A.T.3    Bang-Andersen, B.4    Skrydstrup, T.5
  • 46
    • 84921524253 scopus 로고    scopus 로고
    • C-H activation dependent Pd-catalyzed carbonylative coupling of (hetero)aryl bromides and polyfluoroarenes
    • Lian, Z.; Friis, S. D.; Skrydstrup, T. C-H activation dependent Pd-catalyzed carbonylative coupling of (hetero)aryl bromides and polyfluoroarenes Chem. Commun. 2015, 51, 1870-1873 10.1039/C4CC09303H
    • (2015) Chem. Commun. , vol.51 , pp. 1870-1873
    • Lian, Z.1    Friis, S.D.2    Skrydstrup, T.3
  • 47
    • 84903151681 scopus 로고    scopus 로고
    • Two-Chamber Hydrogen Generation and Application: Access to Pressurized Deuterium Gas
    • Modvig, A.; Andersen, T. L.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. Two-Chamber Hydrogen Generation and Application: Access to Pressurized Deuterium Gas J. Org. Chem. 2014, 79, 5861-5868 10.1021/jo500801t
    • (2014) J. Org. Chem. , vol.79 , pp. 5861-5868
    • Modvig, A.1    Andersen, T.L.2    Taaning, R.H.3    Lindhardt, A.T.4    Skrydstrup, T.5
  • 48
    • 84890124475 scopus 로고    scopus 로고
    • Generation of Stoichiometric Ethylene and Isotopic Derivatives and Application in Transition-Metal-Catalyzed Vinylation and Enyne Metathesis
    • Min, G. K.; Bjerglund, K.; Kramer, S.; Gogsig, T. M.; Lindhardt, A. T.; Skrydstrup, T. Generation of Stoichiometric Ethylene and Isotopic Derivatives and Application in Transition-Metal-Catalyzed Vinylation and Enyne Metathesis Chem.-Eur. J. 2013, 19, 17603-17607 10.1002/chem.201303668
    • (2013) Chem. - Eur. J. , vol.19 , pp. 17603-17607
    • Min, G.K.1    Bjerglund, K.2    Kramer, S.3    Gogsig, T.M.4    Lindhardt, A.T.5    Skrydstrup, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.