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11
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0034741513
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review
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In contrast to other organocuprates, (1-alkoxyvinyl)cuprates have been applied surprisingly little for C-C bond forming reactions; see, e.g. Friesen R.W. J. Chem. Soc., Perkin Trans. 1. 2001;1969-2001. review.
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(2001)
J. Chem. Soc., Perkin Trans. 1
, pp. 1969-2001
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Friesen, R.W.1
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13
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0011928528
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note
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2CuLi (Gilman type), while the opposite was true for cuprates derived from ethyl vinyl ether and methoxyallene, respectively.
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14
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0001334338
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Recent reviews on cuprate chemistry (a) Krause N. Angew. Chem. 109:1997;194-213 (b) Krause N. Angew. Chem. Int., Ed. Engl. 36:1997;186-204 (c) Lipshutz B.H. Schlosser M. Organometallics in Synthesis. 1994;283-382 Wiley, Chichester, (d) Krause N. Modern Organocopper Chemistry. 2002;Wiley/VCH, Weinheim.
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(1997)
Angew. Chem.
, vol.109
, pp. 194-213
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Krause, N.1
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15
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0030902124
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Recent reviews on cuprate chemistry (a) Krause N. Angew. Chem. 109:1997;194-213 (b) Krause N. Angew. Chem. Int., Ed. Engl. 36:1997;186-204 (c) Lipshutz B.H. Schlosser M. Organometallics in Synthesis. 1994;283-382 Wiley, Chichester, (d) Krause N. Modern Organocopper Chemistry. 2002;Wiley/VCH, Weinheim.
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(1997)
Angew. Chem. Int., Ed. Engl.
, vol.36
, pp. 186-204
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Krause, N.1
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16
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0002115585
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Schlosser M., Ed.; Wiley: Chichester
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Recent reviews on cuprate chemistry (a) Krause N. Angew. Chem. 109:1997;194-213 (b) Krause N. Angew. Chem. Int., Ed. Engl. 36:1997;186-204 (c) Lipshutz B.H. Schlosser M. Organometallics in Synthesis. 1994;283-382 Wiley, Chichester, (d) Krause N. Modern Organocopper Chemistry. 2002;Wiley/VCH, Weinheim.
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(1994)
Organometallics in Synthesis
, pp. 283-382
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Lipshutz, B.H.1
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17
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0004246896
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Wiley/VCH: Weinheim
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Recent reviews on cuprate chemistry (a) Krause N. Angew. Chem. 109:1997;194-213 (b) Krause N. Angew. Chem. Int., Ed. Engl. 36:1997;186-204 (c) Lipshutz B.H. Schlosser M. Organometallics in Synthesis. 1994;283-382 Wiley, Chichester, (d) Krause N. Modern Organocopper Chemistry. 2002;Wiley/VCH, Weinheim.
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(2002)
Modern Organocopper Chemistry
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Krause, M.1
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18
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0026698661
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(5,6-Dihydro-4H-pyran-2-yl) lithium undergoes homo-coupling in high yield under the action of copper(II) chloride: Ley S.V., Leslie R., Tiffin P.D., Woods M. Tetrahedron Lett. 33:1992;4767-4770.
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(1992)
Tetrahedron Lett.
, vol.33
, pp. 4767-4770
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Ley, S.V.1
Leslie, R.2
Tiffin, P.D.3
Woods, M.4
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0011927861
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See Ref. 4 for a transformation that appears to include a Lewis acid mediated vinylallene-to-cyclopentadiene isomerization
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See Ref. 4 for a transformation that appears to include a Lewis acid mediated vinylallene-to-cyclopentadiene isomerization.
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21
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0032847813
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(b) Schirmer H., Funke F.J., Müller S., Noltemeyer M., Flynn B.L., de Meijere A. Eur. J. Org. Chem. 1999;2025-2031.
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(1999)
Eur. J. Org. Chem.
, pp. 2025-2031
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Schirmer, H.1
Funke, F.J.2
Müller, S.3
Noltemeyer, M.4
Flynn, B.L.5
De Meijere, A.6
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