Radical synthesis of tetrameric lignin model compound
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关键词:
- Lignin
- / Model compound
- / Tetramer
- / Radical synthesis
English
Radical synthesis of tetrameric lignin model compound
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Key words:
- Lignin
- / Model compound
- / Tetramer
- / Radical synthesis
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[3] A. Wu, B.O. Patrick, E. Chung, B.R. James, Hydrogenolysis of β-O-4 lignin model dimers by a ruthenium-xantphos catalyst, Dalton Trans. 41 (2012) 11093-11106.[3] A. Wu, B.O. Patrick, E. Chung, B.R. James, Hydrogenolysis of β-O-4 lignin model dimers by a ruthenium-xantphos catalyst, Dalton Trans. 41 (2012) 11093-11106.
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[4] V.L. Alves, M.G. Drumond, G.M. Stefani, C.L. Chen, D. Pilo-Veloso, Synthesis of new trimeric lignin model compounds containing 5-5' and β-O-4' substructures, and their characterization by 1D and 2D NMR Techniques, J. Brazil. Chem. Soc. 11 (2000) 467-473.[4] V.L. Alves, M.G. Drumond, G.M. Stefani, C.L. Chen, D. Pilo-Veloso, Synthesis of new trimeric lignin model compounds containing 5-5' and β-O-4' substructures, and their characterization by 1D and 2D NMR Techniques, J. Brazil. Chem. Soc. 11 (2000) 467-473.
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[5] F. Xi, D.W. Reeve, A.B. McKague, The synthesis and chemical structures of tetrameric lignin model compounds, J. Wood Chem. Technol. 16 (1996) 35-46.[5] F. Xi, D.W. Reeve, A.B. McKague, The synthesis and chemical structures of tetrameric lignin model compounds, J. Wood Chem. Technol. 16 (1996) 35-46.
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[6] I. Kilpeläinen, A. Tervilä-Wilo, H. Peräkylä , J. Matikainen, G. Brunow, Synthesis of hexameric lignin model compounds, Holzforschung 48 (1994) 381-386.[6] I. Kilpeläinen, A. Tervilä-Wilo, H. Peräkylä , J. Matikainen, G. Brunow, Synthesis of hexameric lignin model compounds, Holzforschung 48 (1994) 381-386.
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[7] S. Chu, A.V. Subrahmanyam, G.W. Huber, The pyrolysis chemistry of a β-O-4 type oligomeric lignin model compound, Green Chem. 15 (2013) 125-136.[7] S. Chu, A.V. Subrahmanyam, G.W. Huber, The pyrolysis chemistry of a β-O-4 type oligomeric lignin model compound, Green Chem. 15 (2013) 125-136.
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[8] T. Shiba, L. Xiao, T. Miyakoshi, C.L. Chen, Oxidation of isoeugenol and coniferyl alcohol catalyzed by laccases isolated from Rhus vernicifera Stokes and Pycnoporus coccineus, J. Mol. Catal. B: Enzym. 10 (2000) 605-615.[8] T. Shiba, L. Xiao, T. Miyakoshi, C.L. Chen, Oxidation of isoeugenol and coniferyl alcohol catalyzed by laccases isolated from Rhus vernicifera Stokes and Pycnoporus coccineus, J. Mol. Catal. B: Enzym. 10 (2000) 605-615.
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[9] M.S. Dasari, K.M. Richards, M.L. Alt, et al., Synthesis of diapocynin, J. Chem. Educ. 85 (2008) 411-412.[9] M.S. Dasari, K.M. Richards, M.L. Alt, et al., Synthesis of diapocynin, J. Chem. Educ. 85 (2008) 411-412.
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[10] C.J. Liang, C.J. Bruell, M.C. Marley, K.L. Sperry, Persulfate oxidation for in situ remediation of TCE. I. Activated by ferrous ion with and without a persulfate-thiosulfate redox couple, Chemosphere 55 (2004) 1213-1223.[10] C.J. Liang, C.J. Bruell, M.C. Marley, K.L. Sperry, Persulfate oxidation for in situ remediation of TCE. I. Activated by ferrous ion with and without a persulfate-thiosulfate redox couple, Chemosphere 55 (2004) 1213-1223.
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