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13d see: (a) Huerta, F. F.; Gómez, C.; Yus, M. Tetrahedron 1996, 52, 8333-8340.
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(b) Almena, J.; Foubelo, F.; Yus, M. Tetrahedron 1996, 52, 8545-8564.
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(d) Alonso, E.; Guijarro, D.; Yus, M. Tetrahedron 1995, 51, 11457-11464.
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15b,c (a) For a review, see: Nájera, C.; Yus, M. Trends Org. Chem. 1991, 2, 155-181.
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(b) See, for example: Nájera, C.; Yus, M.; Seebach, D. Helv. Chim. Acta. 1984, 67, 289-300.
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(c) For the last paper on this topic from our laboratory, see: Bachki, A.; Foubelo, F.; Yus, M. Tetrahedron: Asymmetry 1995, 6, 1907-1910.
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16. See, for instance: Bates, R. B.; Kroposki, L. M.; Potter, D. E. J. Org. Chem. 1972, 37, 560-562.
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18. See, for instance: Choi, H.; Pinkerton, A. A.; Fry, J. L. J. Chem. Soc., Chem. Commun. 1987, 225-226.
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Choi, H.1
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40
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85030272238
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This type of reaction has been observed in other cases, mainly with oxygenated systems. See, for instance, reference 13d
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19. This type of reaction has been observed in other cases, mainly with oxygenated systems. See, for instance, reference 13d.
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42
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0028314795
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21. Compounds 1a and 1c were prepared by carbonylation of the corresponding amine in the presence of DBU and pyridine, followed by reaction with thionyl chloride in 80 and 76% overall yield, respectively: McGhee, W. D.; Pan, Y.; Talley, J. J. Tetrahedron Lett. 1994, 35, 839-842.
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McGhee, W.D.1
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Talley, J.J.3
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43
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85030273007
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Compound 1e was prepared by direct reaction of thiophosgene with diallylamine in 74% yield: American Cyanamide Co. Br. Patent 683, 141, 1952
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22. Compound 1e was prepared by direct reaction of thiophosgene with diallylamine in 74% yield: American Cyanamide Co. Br. Patent 683, 141, 1952; Chem. Abstr. 1954, 48, 1446c.
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46
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85030274710
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11NS requires M, 141.0612)
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11NS requires M, 141.0612).
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47
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85030272231
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U.S. Patent US 4,518,789, 1986
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26. Yu, R. J.; Van, S. E. J. U.S. Patent US 4,518,789, 1986; Chem. Abstr. 1986, 104, P5648t.
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