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3
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9144232266
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For a monograph, see:. Strohmann C., and Schildbach D. In: Rappoport Z., and Marek I. (Eds). The Chemistry of Organolithium Compounds (2004), Wiley, Chichester, UK 941-996
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Strohmann, C.1
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4
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0000084040
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Dilithium intermediates can be considered functionalised organolithium compounds. For reviews, see:
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Dilithium intermediates can be considered functionalised organolithium compounds. For reviews, see:. Nájera C., and Yus M. Trends Org. Chem. 2 (1991) 155-181
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See also the special issue of Tetrahedron Symposium-in-Print (Nájera, C., Yus, M., Eds.) devoted to 'Functionalised Organolithium Compounds', Tetrahedron. 2005, 61, 3139-3450.
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See also the special issue of Tetrahedron Symposium-in-Print (Nájera, C., Yus, M., Eds.) devoted to 'Functionalised Organolithium Compounds', Tetrahedron. 2005, 61, 3139-3450.
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14
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0004174399
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For general monographs on the preparation of organolithium compounds, see:, Academic, London
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For general monographs on the preparation of organolithium compounds, see:. Wakefield B.J. Organolithium Methods (1988), Academic, London
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0002148313
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Abel E.W., Stone F.G.A., Wilkinson G., and McKillop A. (Eds), Pergamon, Oxford
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Gray M., Tinkel M., and Sniekus V. In: Abel E.W., Stone F.G.A., Wilkinson G., and McKillop A. (Eds). Comprehensive Organometallic Chemistry II Vol. 11 (1995), Pergamon, Oxford 1-92
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In: Rappopoprt Z., and Marek I. (Eds). The Chemistry of Organolithium Compounds (2004), Wiley, Chichester, UK
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Iyoda M., Kabir S.M.H., Vorasingha A., Kuwatami Y., and Yoshida M. Tetrahedron Lett. 39 (1998) 5393-5396
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Kabir S.M.H., Hasegawa M., Kuwatani Y., Yoshida M., Matsuyama H., and Iyoda M. J. Chem. Soc., Perkin Trans. 1 (2001) 159-165
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24
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47149095919
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For the last paper on this topic from our laboratory, see:. Lillo V.J., Gómez C., and Yus M. Tetrahedron Lett. 49 (2008) 5182-5185
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Yus M. In: Rappoport Z., and Marek I. (Eds). The Chemistry of Organolithium Compounds Vol. 1 (2004), J. Wiley & Sons, Chichester Part 2, Chapter 11
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For a polymer supported arene-catalysed version of this reaction, see:. Gómez C., Ruiz S., and Yus M. Tetrahedron Lett. 39 (1998) 1397-1400
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62749186450
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note
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4 and solvents were evaporated in vacuo to yield a residue that was purified by column chromatography (silica gel, hexane-EtOAc) to afford the title products.
-
-
-
-
44
-
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0036169003
-
-
note
-
The monosubstituted products (2, with one E = H) would be formed by abstraction of one hydrogen from the reaction medium (probably from THF at the α-position; see, for instance: Clayden, J.; Yasin, S. A. New J. Chem. 2002, 26, 191-192), before or after quenching with one molecule of the electrophile.
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45
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84984231369
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For additional reactions involving pentaorganosilicates, see:
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For additional reactions involving pentaorganosilicates, see:. Maercker A., and Stötzel R. Chem. Ber. 120 (1987) 1695-1706
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48
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0038729573
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{A figure is presented}
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van Klink G.P.M., de Boer H.J.R., Schat G., Akkerman O.S., Bickelhaupt F., and Spek A.L. Organometallics 21 (2002) 2119-2135 {A figure is presented}
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Spek, A.L.6
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49
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62749103524
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note
-
4 and evaporated in vacuo to afford the pure oxepines 3.
-
-
-
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50
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0004779056
-
-
For reports leading to oxepines of type 3 following different methodologies see, for instance:
-
For reports leading to oxepines of type 3 following different methodologies see, for instance:. Nieger M., Hupfer H., and Bolte M. Acta Crystallogr., Sect C 54 (1998) 656-659
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