-
1
-
-
34748864223
-
-
(a) Soloshonok, V. A.; Mikami, K.; Yamazaki, T.; Welch, J. T.; Honek, J. F. ACS Symp. Ser. 2006, 949.
-
(2006)
ACS Symp. Ser
, vol.949
-
-
Soloshonok, V.A.1
Mikami, K.2
Yamazaki, T.3
Welch, J.T.4
Honek, J.F.5
-
3
-
-
11844274689
-
-
(c) Shimizu, M.; Hiyama, T. Angew. Chem., Int. Ed. 2005, 44, 214-231.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 214-231
-
-
Shimizu, M.1
Hiyama, T.2
-
6
-
-
0742304162
-
-
(f) Mikami, K.; Itoh, Y.; Yamanaka, M. Chem. Rev. 2004, 104, 1-16.
-
(2004)
Chem. Rev
, vol.104
, pp. 1-16
-
-
Mikami, K.1
Itoh, Y.2
Yamanaka, M.3
-
7
-
-
1642365213
-
-
Neilson, A. H, Ed, Springer-Verlag: Berlin
-
(g) Neilson, A. H., Ed. Organofluorines; Springer-Verlag: Berlin, 2002.
-
(2002)
Organofluorines
-
-
-
8
-
-
0003961898
-
-
Springer-Verlag: Berlin
-
(h) Hiyama, T.; Kanie, K.; Kusumoto, T.; Morizawa, Y.; Shimizu, M. Organofluorine Compounds; Springer-Verlag: Berlin, 2000.
-
(2000)
Organofluorine Compounds
-
-
Hiyama, T.1
Kanie, K.2
Kusumoto, T.3
Morizawa, Y.4
Shimizu, M.5
-
10
-
-
0010737617
-
-
Chambers, R. D, Ed, Springer: Berlin
-
(j) Chambers, R. D., Ed. Organofluorine Chemistry; Springer: Berlin, 1997.
-
(1997)
Organofluorine Chemistry
-
-
-
11
-
-
34748927063
-
-
Smart, B. E., Ed. Chem. Rev. 1996, 96, No. 5.
-
(k) Smart, B. E., Ed. Chem. Rev. 1996, 96, No. 5.
-
-
-
-
12
-
-
0003536898
-
-
Banks, R. E, Smart, B. E, Tatlow, J. C, Eds, Plenum Press: New York
-
(l) Banks, R. E., Smart, B. E., Tatlow, J. C., Eds. Organofluorine Chemistry: Principles and Commercial Applications; Plenum Press: New York. 1994.
-
(1994)
Organofluorine Chemistry: Principles and Commercial Applications
-
-
-
13
-
-
0004185069
-
-
Olah, G. A, Prakash, G. K. S, Chambers, R. D, Eds, Wiley: New York
-
(m) Olah, G. A., Prakash, G. K. S., Chambers, R. D., Eds. Synthetic Fluorine Chemistry; Wiley: New York, 1992.
-
(1992)
Synthetic Fluorine Chemistry
-
-
-
14
-
-
0042256378
-
-
Chambers, R. D, Ed, Springer-Verlag: Berlin
-
(a) Burton. D. J.; Lu, L. Topics in Current Chemistry; Chambers, R. D., Ed.; Springer-Verlag: Berlin, 1997, Vol. 193, pp 45-90.
-
(1997)
Topics in Current Chemistry
, vol.193
, pp. 45-90
-
-
Burton, D.J.1
Lu, L.2
-
16
-
-
0141645562
-
-
(c) Knochel, P.; Dohle, W.; Gommermann, N.; Kneisel, F. F.; Kopp, F.; Korn, T.; Sapountzis, I.; Vu, V. A. Angew. Chem., Int. Ed. 2003, 42, 4302-4320.
-
(2003)
Angew. Chem., Int. Ed
, vol.42
, pp. 4302-4320
-
-
Knochel, P.1
Dohle, W.2
Gommermann, N.3
Kneisel, F.F.4
Kopp, F.5
Korn, T.6
Sapountzis, I.7
Vu, V.A.8
-
17
-
-
0000002499
-
-
Reviews on tandem (domino) reactions:, Trost, B. M, Fleming, I, Eds, Pergamon: New York
-
Reviews on tandem (domino) reactions: Ziegler, F. E. In Comprehensive Organic Synthesis, Vol. 6, Trost, B. M., Fleming, I., Eds.; Pergamon: New York, 1991; p 875.
-
(1991)
Comprehensive Organic Synthesis
, vol.6
, pp. 875
-
-
Ziegler, F.E.1
-
19
-
-
34748832938
-
-
Wender, P. A., Ed. Chem. Rev. 1996, 96.
-
Wender, P. A., Ed. Chem. Rev. 1996, 96.
-
-
-
-
21
-
-
34748864855
-
-
Chem. Abstr. 1982, 96, 16001.
-
Chem. Abstr. 1982, 96, 16001.
-
-
-
-
22
-
-
30744477746
-
-
Tandem reductive animation was quite recently reported: Storer, R. I.; Carrera, D. E.; Ni, Y.; MacMillan, D. W. C. J. Am. Chem. Soc. 2006, 128, 84.
-
(a) Tandem reductive animation was quite recently reported: Storer, R. I.; Carrera, D. E.; Ni, Y.; MacMillan, D. W. C. J. Am. Chem. Soc. 2006, 128, 84.
-
-
-
-
23
-
-
13844294033
-
-
Review on asymmetric reductive amination
-
(b) Review on asymmetric reductive amination: Tararov, V. I.; Borner, A. Synlett 2005, 203.
-
(2005)
Synlett
, pp. 203
-
-
Tararov, V.I.1
Borner, A.2
-
24
-
-
0037041333
-
-
Tandem reduction-reductive alkylation of azido sugars: Chen, L.; Wiemer, D. F. Tetrahedron Lett. 2002, 43, 2705.
-
(c) Tandem reduction-reductive alkylation of azido sugars: Chen, L.; Wiemer, D. F. Tetrahedron Lett. 2002, 43, 2705.
-
-
-
-
25
-
-
84984220284
-
-
Tandem alkylative amination of non-enolizable aldehydes with alkyl tris(dialkylamino)titanium reagents: Schiess, M.; Seebach, D. Helv. Chim. Acta 1982, 65, 2598-2602.
-
(d) Tandem alkylative amination of non-enolizable aldehydes with alkyl tris(dialkylamino)titanium reagents: Schiess, M.; Seebach, D. Helv. Chim. Acta 1982, 65, 2598-2602.
-
-
-
-
26
-
-
6044260122
-
-
Itoh, Y.; Yamanaka, M.; Mikami, K. J. Am. Chem. Soc. 2004, 126, 13174-13175.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 13174-13175
-
-
Itoh, Y.1
Yamanaka, M.2
Mikami, K.3
-
27
-
-
34748817558
-
-
Gaussian, Inc, Wallingford, CT
-
Frisch, M. J.; et al. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
-
(2004)
Gaussian 03, revision
, Issue.C.02
-
-
Frisch, M.J.1
-
28
-
-
33745770836
-
-
For Ti- and Li-enolate species, B3LYP/631LAN (LANL2DZ for Ti 6-31G* for others) was adopted. For Ti-ate-enolate, B3LYP/631+LAN (LANL2DZ for Ti, 6-31+G* for others) was adopted. (a) Hay, P. J.; Wadt, W. R. J. Chem. Phys. 1985, 82, 270-283.
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For Ti- and Li-enolate species, B3LYP/631LAN (LANL2DZ for Ti 6-31G* for others) was adopted. For Ti-ate-enolate, B3LYP/631+LAN (LANL2DZ for Ti, 6-31+G* for others) was adopted. (a) Hay, P. J.; Wadt, W. R. J. Chem. Phys. 1985, 82, 270-283.
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-
-
-
31
-
-
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-
-
Wiley: New York, and references cited therein
-
(d) Hehre, W. J.; Radom, L.; von Ragué Schleyer, P.; Pople, J. A. Ab initio Molecular Orbital Theory; Wiley: New York, 1986 and references cited therein.
-
(1986)
Ab initio Molecular Orbital Theory
-
-
Hehre, W.J.1
Radom, L.2
von Ragué Schleyer, P.3
Pople, J.A.4
-
32
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34748858082
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Donation of the lone electron pair of the oxygen to the empty d-orbital of Ti causes the linear multiple bonding see ref 5
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Donation of the lone electron pair of the oxygen to the empty d-orbital of Ti causes the linear multiple bonding (see ref 5).
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-
-
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33
-
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0039664516
-
-
McBee, E. T.; Roberts, C. W.; Meiners, A. F. J. Am. Chem. Soc. 1957, 79, 335-337.
-
(1957)
J. Am. Chem. Soc
, vol.79
, pp. 335-337
-
-
McBee, E.T.1
Roberts, C.W.2
Meiners, A.F.3
-
34
-
-
0000099879
-
-
Scheffold, R, Ed, Verlag: Frankfurt, Germany
-
(a) Seebach, D.; Weidmann, B.; Widler, L. In Modern Synthetic Methods; Scheffold, R., Ed.; Verlag: Frankfurt, Germany, 1983; Vol. 3, pp 217-354.
-
(1983)
Modern Synthetic Methods
, vol.3
, pp. 217-354
-
-
Seebach, D.1
Weidmann, B.2
Widler, L.3
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36
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34748863651
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4 did not give any adduct of benzoate at room temperature for 3 h.
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4 did not give any adduct of benzoate at room temperature for 3 h.
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38
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34748890605
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This reaction mechanism can also be supported by the formation of the perfluoroalkyl adduct of acetone which is derived from isopropoxide
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This reaction mechanism can also be supported by the formation of the perfluoroalkyl adduct of acetone which is derived from isopropoxide.
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39
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34748815725
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When aluminium tri(iso-propoxide) was used for the reaction of perfluoroalkyl metal-ate reagent with aldehyde, no perfluoroalkylation took place
-
When aluminium tri(iso-propoxide) was used for the reaction of perfluoroalkyl metal-ate reagent with aldehyde, no perfluoroalkylation took place.
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