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Penzel, E.1
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Clostridia enzymatically produce hydrocinnamic acid from l-phenylalanine. See
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Clostridia enzymatically produce hydrocinnamic acid from l-phenylalanine. See C. W. Moss M. A. Lambert D. J. Goldsmith Appl. Microbiol. 1970 19 375-378.
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Moss, C.W.1
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85034381910
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Hydrocinnamic acid can also be prepared from cinnamaldehyde, a renewable resource. See, 5 939 581
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Hydrocinnamic acid can also be prepared from cinnamaldehyde, a renewable resource. See A. J. Muller, J. S. Bowers, J. R. I. Eubanks, C. C. Geiger and J. G. Santobianco, US Pat., 5 939 581, 1999.
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Bowers, J.S.2
Eubanks, J.R.I.3
Geiger, C.C.4
Santobianco, J.G.5
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13
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79953832583
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3-cyanopropanoic acid can be prepared from glutamic acid, a biorenewable resource. See
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3-cyanopropanoic acid can be prepared from glutamic acid, a biorenewable resource. See J. Le Nôtre E. L. Scott M. C. R. Franssen J. P. N. Sanders Green Chem. 2011 13 807-809.
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84876888451
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L. Craciun, G. P. Benn, J. Dewing, G. W. Schriver, W. J. Peer, B. Siebenhaar, and U. Siegrist, US Pat. 2005/0222458, 2005.
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Benn, G.P.2
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J. Cason, Organic Syntheses, Wiley & Sons, New York, 1955, vol III, pp 169.
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85034358941
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The separation of styrene from pivalic acid and pivalic anhydride through fractional distillation was unsuccessful due to co-distillation of styrene and pivalic acid and polymerization of styrene
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The separation of styrene from pivalic acid and pivalic anhydride through fractional distillation was unsuccessful due to co-distillation of styrene and pivalic acid and polymerization of styrene.
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33
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85034386722
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2O, and ligands were left open to the atmosphere for 24 h. The hydrocinnamic acid was used as received without purification and left open to the atmosphere for 4 months
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2O, and ligands were left open to the atmosphere for 24 h. The hydrocinnamic acid was used as received without purification and left open to the atmosphere for 4 months.
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-
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34
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85034346221
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2O, and ligands were left open to the atmosphere for 48 h. The hydrocinnamic acid was used as received without purification and left open to the atmosphere for 4 months
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2O, and ligands were left open to the atmosphere for 48 h. The hydrocinnamic acid was used as received without purification and left open to the atmosphere for 4 months.
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35
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37049129819
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The bio-derived substrates levulinic acid, α- and β-angelica lactone can be decarbonylated to methyl vinyl ketone over a solid acid catalyst at high temperatures (290–500 °C), (see J. A. Dumesic, and R. M. West, US Pat. 7 960 592, 2011) as well as photochemically (see,) and in the gas phase through a quartz tube at high temperatures (above 500 °C)
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The bio-derived substrates levulinic acid, α- and β-angelica lactone can be decarbonylated to methyl vinyl ketone over a solid acid catalyst at high temperatures (290–500 °C), (see J. A. Dumesic, and R. M. West, US Pat. 7 960 592, 2011) as well as photochemically (see O. L. Chapman C. L. McIntosh J. Chem. Soc. D 1971 383-384.) and in the gas phase through a quartz tube at high temperatures (above 500 °C).
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J. Chem. Soc. D
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Chapman, O.L.1
McIntosh, C.L.2
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0042048223
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(see,)
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(see Z. P. Xu C. Y. Mok W. S. Chin H. H. Huang S. Li W. Huang J. Chem. Soc., Perkin Trans. 2 1999 725-729.).
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Xu, Z.P.1
Mok, C.Y.2
Chin, W.S.3
Huang, H.H.4
Li, S.5
Huang, W.6
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