-
6
-
-
0000995725
-
-
(c) Roush, W. R.; Walts, A. E.; Hoong, L. K. J. Am. Chem. Soc. 1985, 107, 8186-8190.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 8186-8190
-
-
Roush, W.R.1
Walts, A.E.2
Hoong, L.K.3
-
7
-
-
0345576725
-
-
(d) Boldrini, G. P.; Lodi, L.; Tagliavini, E.; Tarasco, C.; Trombini, C.; Umani-Ronchi, A. J. Org. Chem. 1987, 52, 5447-5452.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 5447-5452
-
-
Boldrini, G.P.1
Lodi, L.2
Tagliavini, E.3
Tarasco, C.4
Trombini, C.5
Umani-Ronchi, A.6
-
8
-
-
33845183116
-
-
(e) Corey, E. J.; Yu, C.-M.; Kim, S. S. J. Am. Chem. Soc. 1989, 111, 5495-5496.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 5495-5496
-
-
Corey, E.J.1
Yu, C.-M.2
Kim, S.S.3
-
9
-
-
0001359587
-
-
(f) Hafner, A.; Duthaler, R. O.; Marti, R.; Rihs, G.; Rothe-Streit, P.; Schwarzenbach, F. J. Am. Chem. Soc. 1992, 114, 2321-2336.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 2321-2336
-
-
Hafner, A.1
Duthaler, R.O.2
Marti, R.3
Rihs, G.4
Rothe-Streit, P.5
Schwarzenbach, F.6
-
11
-
-
0000008279
-
-
(b) Ishihara, K.; Mouri, M.; Gao, Q.; Maruyama, T.; Furuta, K.; Yamamoto, H. J. Am. Chem. Soc. 1993, 115, 11490-11495.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 11490-11495
-
-
Ishihara, K.1
Mouri, M.2
Gao, Q.3
Maruyama, T.4
Furuta, K.5
Yamamoto, H.6
-
13
-
-
0001488391
-
-
4. (a) Keck, G. E.; Tarbet, K. H.; Geraci, L. S. J. Am. Chem. Soc. 1993, 115, 8467-8468.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 8467-8468
-
-
Keck, G.E.1
Tarbet, K.H.2
Geraci, L.S.3
-
15
-
-
33751386025
-
-
(c) Keck, G. E.; Krishnamurthy, D.; Grier, M. C. J. Org. Chem. 1993, 58, 6543-6544.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 6543-6544
-
-
Keck, G.E.1
Krishnamurthy, D.2
Grier, M.C.3
-
16
-
-
12044252883
-
-
(d) Costa, A. L.; Piazza, M. G.; Tagliavini, E.; Trombini, C.; Umani-Ronchi, A. J. Am. Chem. Soc. 1993, 115, 7001-7002.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7001-7002
-
-
Costa, A.L.1
Piazza, M.G.2
Tagliavini, E.3
Trombini, C.4
Umani-Ronchi, A.5
-
17
-
-
0029913899
-
-
5. Recently, chiral poisoning method which allowed the use of inexpensive racemic BINOL has been reported, see: Faller, J. W.; Sams, D. W. I.; Liu, X. J. Am. Chem. Soc. 1996, 118, 1217-1218. And also, for new catalytic system (S)-BINAP-AgOTf (5 mol %), see: Yanagisawa, A.; Nakashima, H.; Ishiba, A.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 4723-4724.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 1217-1218
-
-
Faller, J.W.1
Sams, D.W.I.2
Liu, X.3
-
18
-
-
0029895814
-
-
5. Recently, chiral poisoning method which allowed the use of inexpensive racemic BINOL has been reported, see: Faller, J. W.; Sams, D. W. I.; Liu, X. J. Am. Chem. Soc. 1996, 118, 1217-1218. And also, for new catalytic system (S)-BINAP-AgOTf (5 mol %), see: Yanagisawa, A.; Nakashima, H.; Ishiba, A.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 4723-4724.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 4723-4724
-
-
Yanagisawa, A.1
Nakashima, H.2
Ishiba, A.3
Yamamoto, H.4
-
19
-
-
37049052375
-
-
3SiCl except commercially available phenylthiotrimethylsilane, see: Abel, E. W. J. Chem, Soc. 1960, 4406-4409.
-
(1960)
J. Chem, Soc.
, pp. 4406-4409
-
-
Abel, E.W.1
-
21
-
-
0000826366
-
-
(b) Seebach, D.; Dahinden, R.; Marti, R. E.; Beck, A. K.; Plattner, D. A.; Kühnle, F. N. M. J. Org. Chem. 1995, 60, 1788-1799.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1788-1799
-
-
Seebach, D.1
Dahinden, R.2
Marti, R.E.3
Beck, A.K.4
Plattner, D.A.5
Kühnle, F.N.M.6
-
22
-
-
33751156223
-
-
(b) Haase, C.; Sarko, C. R.; DiMare, M. J. Org. Chem. 1995, 60, 1777-1787.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1777-1787
-
-
Haase, C.1
Sarko, C.R.2
DiMare, M.3
-
23
-
-
0000778829
-
-
4 as observed by Keck in ref.4(a). And also, see: (a) Carreira, E. M.; Lee, W.; Singer, R. A. J. Am. Chem. Soc. 1995, 777, 3649-3650.
-
(1995)
J. Am. Chem. Soc.
, vol.777
, pp. 3649-3650
-
-
Carreira, E.M.1
Lee, W.2
Singer, R.A.3
-
24
-
-
0026738591
-
-
(b) Komatsu, N.; Nishibayashi, Y.; Sugita, T.; Uemura, S. Tetrahedron Lett. 1992, 33, 5391-5394.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 5391-5394
-
-
Komatsu, N.1
Nishibayashi, Y.2
Sugita, T.3
Uemura, S.4
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25
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85030278622
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note
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2 compared with other solvents such as toluene, diethyl ether, and propionitrile.
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26
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85030279196
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note
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10. The O-silylated homoallylic alcohols were isolated in good yields after aqueous work up procedure.
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