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1
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For a review, see: Saavedra, J. E. In Umpoled Synthons, Hase, T. A. Ed.; John Wiley & Sons: New York, 1987; pp. 101-143.
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4
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5044246846
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Broka, C.A.1
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13
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0025957207
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(j) Lohse, P.; Lower, H.; Acklin, P.; Sternfeld, F.; Pfaltz, A. Tetrahedron Lett. 1991, 32, 615-618.
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Lohse, P.1
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0026686960
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(l) Tomooka, K.; Igarashi, T.; Watanabe, M.; Nakai, T. Tetrahedron Lett. 1992, 33, 5795-5798.
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Tomooka, K.1
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Nakai, T.4
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16
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0001166977
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For recent reports, see also
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For a review, see: (a) Cohen, T.; Bhupathy, M. Acc. Chem. Res. 1989, 22, 152-161. For recent reports, see also:
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Cohen, T.1
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23
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0026707977
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(e) Paetow, M.; Ahrens, H.; Hoppe, D. Tetrahedron Lett. 1992, 33, 5323-5326.
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Paetow, M.1
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24
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0026738590
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(f) Ahrens, H.; Paetow, M.; Hoppe, D. Tetrahedron Lett. 1992, 33, 5327-5330.
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Ahrens, H.1
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26
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85031211863
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note
-
An alternative route consists in the transformation of a chloromethyl ether into the corresponding trichlorostannyl derivative followed by low temperature tin/lithium transmetallation with n-butyllithium (ref 4d).
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-
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31
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0342302252
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For the use of a DTBB-catalysed lithiation of a simple alkyl chloride, see: 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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Fry, J.L.3
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32
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0028928103
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See also the accompanying paper in this issue, pp. 1797-1810
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For the last paper on this topic from our laboratory, see: Alonso, E.; Guijarro, D.; Yus, M. Tetrahedron 1995, 51, 2699-2708. See also the accompanying paper in this issue, pp. 1797-1810.
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Tetrahedron
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Alonso, E.1
Guijarro, D.2
Yus, M.3
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33
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0028952540
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See also the accompanying paper in this issue, pp. 1797-1810
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For the last paper on this topic from our laboratory, see: Huerta, F.F.; Gómez, C.; Guijarro, A.; Yus. M. Tetrahedron 1995, 51, 3375-3388. See also the accompanying paper in this issue, pp. 1797-1810.
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Tetrahedron
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Huerta, F.F.1
Gómez, C.2
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Yus, M.4
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34
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0028838031
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See also the accompanying paper in this issue, pp. 1797-1810
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For the last paper on this topic from our laboratory, see: Guijarro, A.; Yus, M. Tetrahedron 1995, 51, 231-234. See also the accompanying paper in this issue, pp. 1797-1810.
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Tetrahedron
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Guijarro, A.1
Yus, M.2
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36
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85031234791
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note
-
2SiCl was used as electrophile, it was necessary to keep the temperature between -90 and -80°C for 30 min before the hydrolysis in order to obtain the best results.
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-
-
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37
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85031234637
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note
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(a) For benzonitrile the temperature was allowed to rise to -60°C for 3 h. (b) In the case of benzonitrile acidification with acetic acid is necessary prior the extraction in order to avoid undesirable by-products.
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41
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0025931439
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Cohen, V. I.; Gibson, R. E.; Fan, L. M.; De la Cruz, R.; Gitler, M. S.; Hariman, E.; Reba, R. C. J. Med. Chem. 1991, 34, 2989-2993.
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Gibson, R.E.2
Fan, L.M.3
De La Cruz, R.4
Gitler, M.S.5
Hariman, E.6
Reba, R.C.7
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42
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0027372541
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Pau, A.; Boatto, G.; Cerri, R.; Palomba, M.; Nicolai, M.; Sparatore, F.; Varoni, M. V. Farmaco 1993, 48, 1291-1299; Chem. Abstr. 1994, 120, 207908u.
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Farmaco
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Pau, A.1
Boatto, G.2
Cerri, R.3
Palomba, M.4
Nicolai, M.5
Sparatore, F.6
Varoni, M.V.7
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43
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0027372541
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Pau, A.; Boatto, G.; Cerri, R.; Palomba, M.; Nicolai, M.; Sparatore, F.; Varoni, M. V. Farmaco 1993, 48, 1291-1299; Chem. Abstr. 1994, 120, 207908u.
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