-
1
-
-
84890597202
-
-
Zhu, J.; Bienaymé, H., Eds.; Wiley-VCH: Weinheim
-
(a) Multicomponent Reactions; Zhu, J.; Bienaymé, H., Eds.; Wiley-VCH: Weinheim, 2005.
-
(2005)
Multicomponent Reactions
-
-
-
3
-
-
0034665244
-
-
(c) Bienaymé, H.; Hulme, C.; Oddon, G.; Schmitt, P. Chem. Eur. J. 2000, 6, 3321.
-
(2000)
Chem. Eur. J.
, vol.6
, pp. 3321
-
-
Bienaymé, H.1
Hulme, C.2
Oddon, G.3
Schmitt, P.4
-
7
-
-
0343081039
-
-
(d) Crousse, B.; Bégué, J.-P.; Bonnet-Delpon, D. J. Org. Chem. 2000, 65, 5009.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 5009
-
-
Crousse, B.1
Bégué, J.-P.2
Bonnet-Delpon, D.3
-
8
-
-
0141665549
-
-
(e) Cheng, D.; Zhou, J.; Saiah, E.; Beaton, G. Org. Lett. 2002, 4, 4411.
-
(2002)
Org. Lett.
, vol.4
, pp. 4411
-
-
Cheng, D.1
Zhou, J.2
Saiah, E.3
Beaton, G.4
-
9
-
-
27944471884
-
-
(f) Zhou, Y.; Jia, X.; Li, R.; Liu, Z.; Liu, Z.; Wu, L. Tetrahedron Lett. 2005, 46, 8937.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8937
-
-
Zhou, Y.1
Jia, X.2
Li, R.3
Liu, Z.4
Liu, Z.5
Wu, L.6
-
10
-
-
33645879237
-
-
(g) Lin, X.-F.; Cui, S.-L.; Wang, Y.-G. Tetrahedron Lett. 2006, 47, 3127.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3127
-
-
Lin, X.-F.1
Cui, S.-L.2
Wang, Y.-G.3
-
11
-
-
27144508168
-
-
(h) See also: Jiménez, O.; de la Rosa, G.; Lavilla, R. Angew. Chem. Int. Ed. 2005, 44, 6521.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6521
-
-
Jiménez, O.1
De La Rosa, G.2
Lavilla, R.3
-
12
-
-
85026863196
-
-
Wiley: New York
-
For some representative examples of the use of fluorous alcohols in organic synthesis, see: (a) Ravikumar, K. S.; Kesavan, V.; Crousse, B.; Bonnet-Delpon, D.; Bégué, J.-P. Organic Syntheses, Vol. 80; Wiley: New York, 2003, 184.
-
(2003)
Organic Syntheses
, vol.80
, pp. 184
-
-
Ravikumar, K.S.1
Kesavan, V.2
Crousse, B.3
Bonnet-Delpon, D.4
Bégué, J.-P.5
-
13
-
-
0037421092
-
-
(b) Spanedda, M. V.; Hoang, V. D.; Crousse, B.; Bonnet-Delpon, D.; Bégué, J.-P. Tetrahedron Lett. 2003, 44, 217.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 217
-
-
Spanedda, M.V.1
Hoang, V.D.2
Crousse, B.3
Bonnet-Delpon, D.4
Bégué, J.-P.5
-
14
-
-
0142089026
-
-
(c) Di Salvo, A.; Spanedda, M. V.; Ourévitch, M.; Crousse, B.; Bonnet-Delpon, D. Synthesis 2003, 2231.
-
(2003)
Synthesis
, pp. 2231
-
-
Di Salvo, A.1
Spanedda, M.V.2
Ourévitch, M.3
Crousse, B.4
Bonnet-Delpon, D.5
-
15
-
-
0345529015
-
-
(d) Magueur, G.; Crousse, B.; Ourévitch, M.; Bégué, J.-P.; Bonnet-Delpon, D. J. Org. Chem. 2003, 68, 9763.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9763
-
-
Magueur, G.1
Crousse, B.2
Ourévitch, M.3
Bégué, J.-P.4
Bonnet-Delpon, D.5
-
16
-
-
0032563923
-
-
TFE has already been used as a superior solvent in other MCR's: (e) Park, S. J.; Keum, G.; Kang, S. B.; Koh, H. Y.; Kim, Y.; Lee, D. H. Tetrahedron Lett. 1998, 39, 7109.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 7109
-
-
Park, S.J.1
Keum, G.2
Kang, S.B.3
Koh, H.Y.4
Kim, Y.5
Lee, D.H.6
-
17
-
-
0035856895
-
-
(f) Cristau, P.; Vors, J.-P.; Zhu, J. Org. Lett 2001, 3, 4079.
-
(2001)
Org. Lett
, vol.3
, pp. 4079
-
-
Cristau, P.1
Vors, J.-P.2
Zhu, J.3
-
19
-
-
34548027483
-
-
Gladysz, J. A.; Curran, D. P.; Horvath, I. T., Eds.; Wiley-VCH: Weinheim
-
(b) Bégué, J.-P.; Bonnet-Delpon, D.; Crousse, B. In Handbook of Fluorous Chemistry; Gladysz, J. A.; Curran, D. P.; Horvath, I. T., Eds.; Wiley-VCH: Weinheim, 2004, 341.
-
(2004)
Handbook of Fluorous Chemistry
, pp. 341
-
-
Bégué, J.-P.1
Bonnet-Delpon, D.2
Crousse, B.3
-
20
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33747044071
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note
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In the presence of styrene or N-vinyl pyrrolidine as dienophile, no reaction occurred over 24 h, while the alkyl aldimine decomposed in the medium.
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-
-
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21
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33747061507
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note
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21NO (219.32): C, 76.67; H, 9.65; N, 6.39. Found: C, 76.33; H, 9.99; N, 6.35.
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-
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24
-
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27944484901
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-
and references therein
-
Haidekker, M. A.; Brady, T. P.; Lichlyter, D.; Theodorakis, E. A. Bioorg. Chem. 2005, 33, 415; and references therein.
-
(2005)
Bioorg. Chem.
, vol.33
, pp. 415
-
-
Haidekker, M.A.1
Brady, T.P.2
Lichlyter, D.3
Theodorakis, E.A.4
-
26
-
-
2642592978
-
-
Wiley: New York
-
(a) Glass, D. B.; Weissberger, A. Org. Synth., Coll. Vol. III; Wiley: New York, 1955, 504.
-
(1955)
Org. Synth., Coll. Vol. III
, vol.3
, pp. 504
-
-
Glass, D.B.1
Weissberger, A.2
-
27
-
-
84986437192
-
-
(b) Katayama, H.; Abe, E.; Kaneko, K. J. Heterocycl. Chem. 1982, 19, 925.
-
(1982)
J. Heterocycl. Chem.
, vol.19
, pp. 925
-
-
Katayama, H.1
Abe, E.2
Kaneko, K.3
-
28
-
-
0035801827
-
-
See also: (c) Palma, A.; Carrillo, C.; Stashenko, E.; Kouznetsov, V.; Bahsas, A.; Amaro-Luis, J. Tetrahedron Lett. 2001, 42, 6247.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 6247
-
-
Palma, A.1
Carrillo, C.2
Stashenko, E.3
Kouznetsov, V.4
Bahsas, A.5
Amaro-Luis, J.6
-
29
-
-
0037152588
-
-
(d) Palma, A.; Agredo, J. S.; Carrillo, C.; Kouznetsov, V.; Stashenko, E.; Bahsas, A.; Amaro-Luis, J. Tetrahedron 2002, 58, 8719.
-
(2002)
Tetrahedron
, vol.58
, pp. 8719
-
-
Palma, A.1
Agredo, J.S.2
Carrillo, C.3
Kouznetsov, V.4
Stashenko, E.5
Bahsas, A.6
Amaro-Luis, J.7
-
30
-
-
0029896913
-
-
(a) Katritzky, A. R.; Rachwal, B.; Rachwal, S. J. Org. Chem. 1996, 61, 3117.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3117
-
-
Katritzky, A.R.1
Rachwal, B.2
Rachwal, S.3
-
31
-
-
0033617174
-
-
(b) Katritzky, A. R.; Luo, Z.; Cui, X.-L. J. Org. Chem. 1999, 64, 3328.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3328
-
-
Katritzky, A.R.1
Luo, Z.2
Cui, X.-L.3
-
32
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33747048884
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note
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3): δ = 15.6, 15.7, 17.2, 20.5, 27.0, 27.5, 29.0, 42.6, 62.0, 63.3, 63.7, 73.0, 73.9, 114.9, 121.7, 122.6, 128.2, 129.5, 142.1.
-
-
-
-
33
-
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33747070176
-
-
note
-
The cis-configuration was established by means of NOE experiments (NOESY) on product 3. The correlations are shown on the under drawing. Relative configurations of products 2 and 4 have been deduced by analogy (Figure 2).
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