-
1
-
-
24044470646
-
-
For recent reviews, see: a
-
For recent reviews, see: a) C.-J. Li, Chem. Rev. 2005, 105, 3095;
-
(2005)
Chem. Rev
, vol.105
, pp. 3095
-
-
Li, C.-J.1
-
3
-
-
1042275565
-
-
c) V. Nair, S. Ros, C. N. Jayan, B. S. Pillai, Tetrahedron 2004, 60, 1959;
-
(2004)
Tetrahedron
, vol.60
, pp. 1959
-
-
Nair, V.1
Ros, S.2
Jayan, C.N.3
Pillai, B.S.4
-
9
-
-
0003768632
-
-
Eds, P. Anastas, T. Williamson, Oxford University Press, New York
-
i) L. A. Paquette, Green Chemistry: Frontiers in Benign Chemical Synthesis and Processing (Eds.: P. Anastas, T. Williamson), Oxford University Press, New York, 1998;
-
(1998)
Green Chemistry: Frontiers in Benign Chemical Synthesis and Processing
-
-
Paquette, L.A.1
-
13
-
-
0037433942
-
-
c) T.-P. Loh, M.-J. Lin, K.-L. Tan, Tetrahedron Lett. 2003, 44, 507;
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 507
-
-
Loh, T.-P.1
Lin, M.-J.2
Tan, K.-L.3
-
16
-
-
6044221426
-
-
f) W. Miao, L. W. Chung, T. H. Chan, J. Am. Chem. Soc. 2004, 126, 13326.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 13326
-
-
Miao, W.1
Chung, L.W.2
Chan, T.H.3
-
17
-
-
28944440168
-
-
For selected examples, see: a
-
For selected examples, see: a) U. Schneider, M. Sugiura, S. Kobayashi, Tetrahedron 2006, 62, 496;
-
(2006)
Tetrahedron
, vol.62
, pp. 496
-
-
Schneider, U.1
Sugiura, M.2
Kobayashi, S.3
-
19
-
-
0037530087
-
-
c) S. Konishi, H. Hanawa, K. Maruoka, Tetrahedron: Asymmetry 2003, 14, 1603;
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 1603
-
-
Konishi, S.1
Hanawa, H.2
Maruoka, K.3
-
20
-
-
0035814327
-
-
d) D. A. Evans, Z. K. Sweeney, T. Rovis, J. S. Tedrow, J. Am. Chem. Soc. 2001, 123, 12095;
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 12095
-
-
Evans, D.A.1
Sweeney, Z.K.2
Rovis, T.3
Tedrow, J.S.4
-
21
-
-
0035900403
-
-
e) A. McCluskey, I. W. Muderawan, Muntari, D. J. Young, J. Org. Chem. 2001, 66, 7811;
-
(2001)
J. Org. Chem
, vol.66
, pp. 7811
-
-
McCluskey, A.1
Muderawan, I.W.2
Muntari3
Young, D.J.4
-
22
-
-
0035925234
-
-
f) M. Hojo, R. Sakuragi, S. Okabe, A. Hosomi, Chem. Commun. 2001, 357;
-
(2001)
Chem. Commun
, pp. 357
-
-
Hojo, M.1
Sakuragi, R.2
Okabe, S.3
Hosomi, A.4
-
23
-
-
0034699991
-
-
g) Y. Masuyama, A. Watabe, A. Ito, Y. Kurusu, Chem. Commun. 2000, 2009;
-
(2000)
Chem. Commun
, pp. 2009
-
-
Masuyama, Y.1
Watabe, A.2
Ito, A.3
Kurusu, Y.4
-
24
-
-
0032544714
-
-
h) C.-M. Yu, S.-K. Yoon, K. Baek, J.-Y. Lee, Angew. Chem. Int. Ed. 1998, 37, 2392.
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 2392
-
-
Yu, C.-M.1
Yoon, S.-K.2
Baek, K.3
Lee, J.-Y.4
-
25
-
-
38349136108
-
-
See ref.[2f] and references cited therein
-
[2f] and references cited therein.
-
-
-
-
26
-
-
13644257604
-
-
For examples, see: a
-
For examples, see: a) J. Kjellgren, H. Sundén, K. J. Szabó, J. Am. Chem. Soc. 2005, 127, 1787;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 1787
-
-
Kjellgren, J.1
Sundén, H.2
Szabó, K.J.3
-
28
-
-
0345825802
-
-
c) J. Kjellgren, H. Sundén, K. J. Szabó, J. Am. Chem. Soc. 2004, 126, 474;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 474
-
-
Kjellgren, J.1
Sundén, H.2
Szabó, K.J.3
-
30
-
-
38349174630
-
-
4. The solvent was evaporated, and the residue was subjected to NMR analysis.
-
4. The solvent was evaporated, and the residue was subjected to NMR analysis.
-
-
-
-
31
-
-
0026530298
-
-
a) S. Araki, A. Imai, K. Shimizu, Y. Butsugan, Tetrahedron Lett. 1992, 33, 2581;
-
(1992)
Tetrahedron Lett
, vol.33
, pp. 2581
-
-
Araki, S.1
Imai, A.2
Shimizu, K.3
Butsugan, Y.4
-
32
-
-
0000656554
-
-
b) S. Araki, A. Imai, K. Shimizu, M. Yamada, A. Mori, Y. Butsugan, J. Org. Chem. 1995, 60, 1841;
-
(1995)
J. Org. Chem
, vol.60
, pp. 1841
-
-
Araki, S.1
Imai, A.2
Shimizu, K.3
Yamada, M.4
Mori, A.5
Butsugan, Y.6
-
36
-
-
38349184669
-
-
The ratio of 5a/4a was 1:2, and the mixture was obtained from the In-mediated coupling of hydrocinnamyl aldehyde with propargylic bromide in water. See ref.[2a
-
[2a]
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37
-
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38349167119
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4. The solvent was evaporated, and the residue was subjected to NMR analysis.
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4. The solvent was evaporated, and the residue was subjected to NMR analysis.
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