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1
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0036703508
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For a recent review on organic reactions in water, see: (a) Lindström, U. M. Chem. Rev. 2002, 102, 2751. See also: (b) Li, C. J.; Chan, T. H. Organic Reactions in Aqueous Media; John Wiley & Sons: New York, 1997; (c) Cornils, B.; Herrmann, W. A., Eds., Aqueous-Phase Organometallic Catalysis; Wiley-VCH: Weinheim, 1998; (d) Filmore, D. Today's Chem. Work 2002, 11, 29.
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Chem. Rev.
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Lindström, U.M.1
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2
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0003602022
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John Wiley & Sons: New York
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For a recent review on organic reactions in water, see: (a) Lindström, U. M. Chem. Rev. 2002, 102, 2751. See also: (b) Li, C. J.; Chan, T. H. Organic Reactions in Aqueous Media; John Wiley & Sons: New York, 1997; (c) Cornils, B.; Herrmann, W. A., Eds., Aqueous-Phase Organometallic Catalysis; Wiley-VCH: Weinheim, 1998; (d) Filmore, D. Today's Chem. Work 2002, 11, 29.
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(1997)
Organic Reactions in Aqueous Media
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Li, C.J.1
Chan, T.H.2
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3
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0003476436
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Wiley-VCH: Weinheim
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For a recent review on organic reactions in water, see: (a) Lindström, U. M. Chem. Rev. 2002, 102, 2751. See also: (b) Li, C. J.; Chan, T. H. Organic Reactions in Aqueous Media; John Wiley & Sons: New York, 1997; (c) Cornils, B.; Herrmann, W. A., Eds., Aqueous-Phase Organometallic Catalysis; Wiley-VCH: Weinheim, 1998; (d) Filmore, D. Today's Chem. Work 2002, 11, 29.
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(1998)
Aqueous-Phase Organometallic Catalysis
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Cornils, B.1
Herrmann, W.A.2
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4
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0012590551
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For a recent review on organic reactions in water, see: (a) Lindström, U. M. Chem. Rev. 2002, 102, 2751. See also: (b) Li, C. J.; Chan, T. H. Organic Reactions in Aqueous Media; John Wiley & Sons: New York, 1997; (c) Cornils, B.; Herrmann, W. A., Eds., Aqueous-Phase Organometallic Catalysis; Wiley-VCH: Weinheim, 1998; (d) Filmore, D. Today's Chem. Work 2002, 11, 29.
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(2002)
Today's Chem. Work
, vol.11
, pp. 29
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Filmore, D.1
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8
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0032491869
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Sugihara T., Yamada M., Ban H., Yamaguchi M., Kaneko C. Angew. Chem., Int. Ed. Engl. 36:1997;2801.
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Angew. Chem., Int. Ed. Engl.
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Sugihara, T.1
Yamada, M.2
Ban, H.3
Yamaguchi, M.4
Kaneko, C.5
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9
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0000266263
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Son S.U., Lee S.I., Chung Y.K., Kim S.W., Hyeon T. Org. Lett. 4:2002;277.
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Org. Lett.
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Son, S.U.1
Lee, S.I.2
Chung, Y.K.3
Kim, S.W.4
Hyeon, T.5
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10
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85031201663
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note
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6 complex before the introduction of water. A small amount of Celite was added into these reaction mixtures to facilitate stirring and to adsorb cobalt residues after the reaction. Insignificant differences in the yields were observed when Celite was not added to the reaction mixture.
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11
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0346461917
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Cyclodextrins are cyclic oligosaccharides consisting of six (α-CD), seven (β-CD), and eight (γ-CD) glucopyranose units and possessing both hydrophilic and hydrophobic sites. For a background on cyclodextrins, see:
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Cyclodextrins are cyclic oligosaccharides consisting of six (α-CD), seven (β-CD), and eight (γ-CD) glucopyranose units and possessing both hydrophilic and hydrophobic sites. For a background on cyclodextrins, see: Szejtli J. Chem. Rev. 98:1998;1743.
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Szejtli, J.1
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13
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85031201570
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2, 25% EtOAc in hexanes) provided 35 mg of ketone 23 (59% yield).
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2, 25% EtOAc in hexanes) provided 35 mg of ketone 23 (59% yield).
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14
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0037154772
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Chung observed that enyne 1 bearing a terminal alkyne moiety provided minor amounts of the ketone 24 using colloidal cobalt nanoparticles in aqueous media. See Ref. 6 and also: (a) Krafft, M. E.; Boñaga, L. V. R.; Wright, J. A.; Hirosawa, C. J. Org. Chem. 2002, 67, 1233; (b) Krafft, M. E.; Boñaga, L. V. R. Angew. Chem., Int. Ed. 2000, 39, 3676.
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Org. Chem.
, vol.67
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Krafft, M.E.1
Boñaga, L.V.R.2
Wright, J.A.3
Hirosawa, C.J.4
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15
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0034675661
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Chung observed that enyne 1 bearing a terminal alkyne moiety provided minor amounts of the ketone 24 using colloidal cobalt nanoparticles in aqueous media. See Ref. 6 and also: (a) Krafft, M. E.; Boñaga, L. V. R.; Wright, J. A.; Hirosawa, C. J. Org. Chem. 2002, 67, 1233; (b) Krafft, M. E.; Boñaga, L. V. R. Angew. Chem., Int. Ed. 2000, 39, 3676.
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(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 3676
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Krafft, M.E.1
Boñaga, L.V.R.2
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16
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85031206848
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note
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abstract
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