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For an alternative formylation procedure on EDOT, see
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For an alternative formylation procedure on EDOT, see: Mohanakrishnan, A. K.; Hucke, A.; Lyon, M. A.; Laksmikantham, M. V.; Cava, M. P. Tetrahedron 1999, 55, 11745-11754.
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0026763993
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For an example of a general procedure for iodine-mediated oxidation of aldehydes to carboxylic acids, see
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0035323796
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Jung, C. M.; Kraus, W.; Leibnitz, P.; Pietzsch, H. J.; Kropp, J.; Spies, H. Eur. J. Inorg. Chem. 2002, 1219-1225.
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18
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33750431472
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No cleavage yields are reported for cleavage with TFMSA as they did not give higher yields than for similar concentrations of TFA
-
No cleavage yields are reported for cleavage with TFMSA as they did not give higher yields than for similar concentrations of TFA.
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19
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0012376090
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0041657876
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For the synthesis of secondary amines on the p-BAL handle, see
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For the synthesis of secondary amines on the p-BAL handle, see: Forns, P.; Sevilla, S.; Erra, M.; Ortega, A.; Fernández, J.-C.; de la Figuera, N.; Fernández-Forner, D.; Albericio, F. Tetrahedron Lett. 2003, 44, 6907-6910.
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De La Figuera, N.6
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23
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33750492375
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note
-
The correct IUPAC nomenclature for this compound is 2,3-dihydrothieno [3,4-6][1,4] dioxine-5-carbaldehyde, but for this and the following compounds the more brief "EDOT-nomenclature" will be applied.
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24
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0033617384
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Tok, J. B. H.; Cho, J.; Rando, R. R. Tetrahedron 1999, 55, 5741-5758.
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Rando, R.R.3
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25
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33750450104
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note
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Alternatively, 10% aqueous citric acid can be used in order to give a milder acidification of the reaction mixture.
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