-
8
-
-
0030668118
-
-
CO = 30 atm, 90 °C, 24 h: N. Jeong, S.H. Hwang, Y.W. Lee, and J.S. Lim. J. Am. Chem. Soc. 119, 10 549 (1997);
-
(1997)
J. Am. Chem. Soc.
, vol.119
, Issue.10
, pp. 549
-
-
Jeong, N.1
Hwang, S.H.2
Lee, Y.W.3
Lim, J.S.4
-
10
-
-
0003826570
-
-
Oxford University Press, Oxford
-
Development of cost-effective, safe, and environmentally benign organic processes has been an increasing research focus. (a) P. Tundo and P.T. Anastas. Green chemistry: Challenging perpectives. Oxford University Press, Oxford. 2000;
-
(2000)
Green Chemistry: Challenging Perpectives
-
-
Tundo, P.1
Anastas, P.T.2
-
12
-
-
1642284120
-
-
For recent reviews, see: (a) J. Blanco-Urgoiti, L. Añorbe, L. Perez-Serrano, G. Dominguez, and J. Perez-Castells. Chem. Soc. Rev. 33, 32 (2004);
-
(2004)
Chem. Soc. Rev.
, vol.33
, pp. 32
-
-
Blanco-Urgoiti, J.1
Añorbe, L.2
Perez-Serrano, L.3
Dominguez, G.4
Perez-Castells, J.5
-
16
-
-
0037198748
-
-
(b) K.M. Brummond, H. Chen, K.D. Fisher, A.D. Kerekes, B. Rickards, P.C. Sill, and S.J. Geib. Org. Lett. 4, 1931 (2002);
-
(2002)
Org. Lett.
, vol.4
, pp. 1931
-
-
Brummond, K.M.1
Chen, H.2
Fisher, K.D.3
Kerekes, A.D.4
Rickards, B.5
Sill, P.C.6
Geib, S.J.7
-
17
-
-
0008924882
-
-
Edited by M. Harmata. JAI Press Inc., Greenwich, Connecticut
-
(c) K.M. Brummond. In Advances in cycloaddition chemistry. Vol 6. Edited by M. Harmata. JAI Press Inc., Greenwich, Connecticut. 1999. p. 211.
-
(1999)
Advances in Cycloaddition Chemistry
, vol.6
, pp. 211
-
-
Brummond, K.M.1
-
21
-
-
0032491869
-
-
4OH (1:3, v/v): T. Sugihara, M. Yamada, H. Ban, M. Yamaguchi, and C. Kaneko. Angew. Chem. Int. Ed. Engl. 36, 2801 (1997).
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 2801
-
-
Sugihara, T.1
Yamada, M.2
Ban, H.3
Yamaguchi, M.4
Kaneko, C.5
-
22
-
-
0000266263
-
-
Stabilized cobalt nanoparticles, water, sodium dodecyl sulfate, 20 atm CO, 130 °C, 12 h: S.U. Son, S.I. Lee, Y.K. Chung, S.W. Kim, and T. Hyeon. Org. Lett. 4, 277 (2002).
-
(2002)
Org. Lett.
, vol.4
, pp. 277
-
-
Son, S.U.1
Lee, S.I.2
Chung, Y.K.3
Kim, S.W.4
Hyeon, T.5
-
23
-
-
0038408913
-
-
2, 10 mol% dppp, 10 mol% TPPTS, 2 mol equiv. SDS, water, 100 °C, nitrogen, 2-12 h: F. Koji, T. Morimoto, K. Tsutsumi, and K. Kakiuchi. Angew. Chem. Int. Ed. 42, 2409 (2003).
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2409
-
-
Koji, F.1
Morimoto, T.2
Tsutsumi, K.3
Kakiuchi, K.4
-
24
-
-
0142025317
-
-
2, 6 mol% BINAP, water-dioxane (1:1), 90 °C, 1.5 h: W.H. Suh, M. Choi, S.I. Lee, and Y.K. Chung. Synthesis, 2169 (2003).
-
(2003)
Synthesis
, pp. 2169
-
-
Suh, W.H.1
Choi, M.2
Lee, S.I.3
Chung, Y.K.4
-
27
-
-
0000316894
-
-
Edited by E.W. Abel, F.A. Stone, and G. Wilkinson. Pergamon Press, Oxford
-
(b) R.D.W. Kemmitt and D.R. Russell. In Comprehensive organometallic chemistry. Vol 5. Edited by E.W. Abel, F.A. Stone, and G. Wilkinson. Pergamon Press, Oxford. 1982. p. 7.
-
(1982)
Comprehensive Organometallic Chemistry
, vol.5
, pp. 7
-
-
Kemmitt, R.D.W.1
Russell, D.R.2
-
28
-
-
0032556207
-
-
3, has been exploited by the Sugihara laboratory. For Pauson-Khand reactions: (a) T. Sugihara and M. Yamaguchi. J. Am. Chem. Soc. 120, 10 782 (1998);
-
(1998)
J. Am. Chem. Soc.
, vol.120
, Issue.10
, pp. 782
-
-
Sugihara, T.1
Yamaguchi, M.2
-
30
-
-
0037149440
-
-
3-CH) in alkyne cyclotrimerizations: (c) T. Sugihara, A. Wakabayashi, Y. Nagai, H. Takao, H. Imagawa, and M. Nishizawa. Chem. Commun. 576 (2002).
-
(2002)
Chem. Commun.
, pp. 576
-
-
Sugihara, T.1
Wakabayashi, A.2
Nagai, Y.3
Takao, H.4
Imagawa, H.5
Nishizawa, M.6
-
31
-
-
0035824367
-
-
For cyclopentadienone synthesis: (d) T. Sugihara, A. Wakabayashi, H. Takao, H. Imagawa, and M. Nishizawa. Chem. Commun. 2456 (2001).
-
(2001)
Chem. Commun.
, pp. 2456
-
-
Sugihara, T.1
Wakabayashi, A.2
Takao, H.3
Imagawa, H.4
Nishizawa, M.5
-
34
-
-
0032577036
-
-
N. Iwasawa, T. Matsuo, M. Iwamoto, and T. Ikeno. J. Am. Chem. Soc. 120, 3903 (1998).
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 3903
-
-
Iwasawa, N.1
Matsuo, T.2
Iwamoto, M.3
Ikeno, T.4
-
36
-
-
0043127202
-
-
A. Oledra, C.-J. Wu, R.J. Madhushaw, S.-L. Wang, and R.-S. Liu. J. Am. Chem. Soc. 125, 9610 (2003).
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 9610
-
-
Oledra, A.1
Wu, C.-J.2
Madhushaw, R.J.3
Wang, S.-L.4
Liu, R.-S.5
-
38
-
-
0031936070
-
-
12 in the PK reaction was also briefly mentioned in a reaction using supercritical fluid (3).
-
(1998)
Synthesis
, pp. 142
-
-
Kim, J.W.1
Chung, Y.K.2
-
39
-
-
0037154772
-
-
(a) M.E. Krafft, L.V.R. Boñaga, J.A. Wright, and C. Hirosawa. J. Org. Chem. 67, 1233 (2002);
-
(2002)
J. Org. Chem.
, vol.67
, pp. 1233
-
-
Krafft, M.E.1
Boñaga, L.V.R.2
Wright, J.A.3
Hirosawa, C.4
-
42
-
-
4644324093
-
-
For a review of side reactions observed under the PK reaction conditions, see: (a) L.V.R. Boñaga and M.E. Krafft. Tetrahedron, 60, 9795 (2004).
-
(2004)
Tetrahedron
, vol.60
, pp. 9795
-
-
Boñaga, L.V.R.1
Krafft, M.E.2
-
45
-
-
0034595752
-
-
(d) L. Pérez-Serrano, J. Blanco-Urgoiti, L. Casarrubios, G. Dominguez, and J. Pérez-Castells. J. Org. Chem. 65, 3513 (2000);
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3513
-
-
Pérez-Serrano, L.1
Blanco-Urgoiti, J.2
Casarrubios, L.3
Dominguez, G.4
Pérez-Castells, J.5
-
50
-
-
0346461917
-
-
Cyclodextrins (CD) are cyclic oligosaccharides consisting of six (α-CD), seven (β-CD), and eight (γ-CD) glucopyranose units and possessing both hydrophilic and hydrophobic sites. The cyclodextrin cavity is slightly apolar so that when it is occupied by polar water molecules it can be energetically unfavorable. Because of this negative interaction, the water molecules can be substituted by the less polar molecules in a host-guest manner. The cyclodextrin molecule usually can trap one guest molecule so that it can theoretically improve the normally unfavorable environment that exists with a poorly soluble molecule and the aqueous solution. The reactivity of the trapped molecule can either decreased because of stabilization or be enhanced in other cases. For a background on cyclodextrins, see: J. Szejtli. Chem. Rev. 98, 1743 (1998).
-
(1998)
Chem. Rev.
, vol.98
, pp. 1743
-
-
Szejtli, J.1
-
52
-
-
85029867296
-
-
(b) N. Jeong, Y.K. Chung, B.Y. Lee, S.H. Lee, and S.-E. Yoo. Synlett, 204 (1991).
-
(1991)
Synlett
, pp. 204
-
-
Jeong, N.1
Chung, Y.K.2
Lee, B.Y.3
Lee, S.H.4
Yoo, S.-E.5
-
53
-
-
0030746742
-
-
T. Kondo, N. Suzuki, T. Okada, and T. Mitsudo. J. Am. Chem. Soc. 119, 6187 (1997).
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 6187
-
-
Kondo, T.1
Suzuki, N.2
Okada, T.3
Mitsudo, T.4
|