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13
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0000298547
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1,2-Dehalogenation and Related Reactions
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S. Patai Z. Rappoport John Wiley New York
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E. Baciocchi 1,2-Dehalogenation and Related Reactions S. Patai Z. Rappoport The Chemistry of Functional Groups, Supplement D, Part I 1983 John Wiley New York 161 201
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Baciocchi, E.1
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23
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30544441796
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note
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1H NMR analysis of crude reaction mixtures, to determine the percentage of deuterium incorporation in the arylmethyl positions. See Ref. 4.
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25
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30544431584
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note
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1H NMR to determine the exact amount of trans-stilbazole, this mixture can be successfully recycled to a new reductive dehalogenation reaction.
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27
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30544450051
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Chem. Zentralbl. 106 1935 2358
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Chem. Zentralbl.
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, pp. 2358
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28
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30544434028
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Chem. Abs. 29 1935 1062
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Chem. Abs.
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29
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30544449328
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See also: G. Rankoff Chem. Ber. 63 1930 2139 2142
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Chem. Ber.
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, pp. 2139-2142
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Rankoff, G.1
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30
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30544432952
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note
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Similar results were obtained employing 1a as a reducing agent; however, the employment of 1b allowed an easier purification of reaction products.
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31
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30544454251
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The trans stereochemistry of amide 2f, was assigned by comparison with the stereochemistry of the corresponding N-carboxamide and N-carbonyl chloride, prepared under similar reaction conditions: G. Bellucci, C. Chiappe, F. Marioni, and F. Marchetti J. Chem. Soc., Perkin Trans. 2 1992 637 642 and references cited therein
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(1992)
J. Chem. Soc., Perkin Trans. 2
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Bellucci, G.1
Chiappe, C.2
Marioni, F.3
Marchetti, F.4
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33
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30544438446
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note
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Alternative reductive elimination mechanisms are usually described as 'single electron' or as 'concerted two electrons' reaction pathways. For an in-depth comparison of these mechanisms, see Ref. 5c.
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