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1
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64349116571
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Reviews on domino reaction
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Reviews on domino reaction:
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2
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7044235263
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(a) Tietze, L. F. Chem. Rev. 1996, 96, 115-136.
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(1996)
Chem. Rev
, vol.96
, pp. 115-136
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Tietze, L.F.1
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4
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0037423972
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For reviews on domino, cascade reactions in total synthesis see: a
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For reviews on domino, cascade reactions in total synthesis see: (a) Nicolaou, K. C; Montagnon, T.; Snyder, S. A. Chem. Comm. 2003, 551-564.
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(2003)
Chem. Comm
, pp. 551-564
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Nicolaou, K.C.1
Montagnon, T.2
Snyder, S.A.3
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5
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33750977591
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Nicolaou, K. C; Edmonds, D. J.; Bulger, P. G. Ansew. Chem., Int. Ed. 2006, 45, 7134-7186.
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(b) Nicolaou, K. C; Edmonds, D. J.; Bulger, P. G. Ansew. Chem., Int. Ed. 2006, 45, 7134-7186.
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8
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64349120261
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For reviews on reductive-aldol reactions see
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For reviews on reductive-aldol reactions see:
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9
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4544221000
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(a) Chiu, P. Synthesis 2004, 2210-2215.
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(2004)
Synthesis
, pp. 2210-2215
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Chiu, P.1
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10
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34347225080
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Selected references: for intermolecular reductive-aldol reaction [Rh
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(b) Nishiyama, H.; Shiomi, T. Toy. Curr. Chem. 2007, 279, 105-137. Selected references: for intermolecular reductive-aldol reaction [Rh]:
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(2007)
Toy. Curr. Chem
, vol.279
, pp. 105-137
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Nishiyama, H.1
Shiomi, T.2
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12
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0034630894
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(d) Taylor, S. J.; Duffey, M. O.; Morken, J. P. J. Am. Chem. Soc. 2000, 122, 4528-4529.
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J. Am. Chem. Soc
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Taylor, S.J.1
Duffey, M.O.2
Morken, J.P.3
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13
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18744395482
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(e) Nishiyama, H.; Shiomi, T.; Tsuchiya, Y.; Matsuda, I. J. Am. Chem. Soc. 2005, 127, 6972-6973.
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(2005)
J. Am. Chem. Soc
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Nishiyama, H.1
Shiomi, T.2
Tsuchiya, Y.3
Matsuda, I.4
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14
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0037176242
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(f) Jang, H.-Y.; Huddleston, R. R.; Krische, M. J. J. Am. Chem. Soc. 2002, 124, 15156-15157.
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(2002)
J. Am. Chem. Soc
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Jang, H.-Y.1
Huddleston, R.R.2
Krische, M.J.3
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16
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40949114623
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Ir
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(h) Bee, C; Han, S. B.; Hassan, A.; Lida, H.; Krische, M. J. J. Am. Chem. Soc. 2008, 130, 2746-2747 [Ir]:
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(2008)
J. Am. Chem. Soc
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, pp. 2746-2747
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Bee, C.1
Han, S.B.2
Hassan, A.3
Lida, H.4
Krische, M.J.5
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17
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0001494417
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Co
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(i) Zhao, C. X.; Duffey, M. O.; Taylor, S. J.; Morken, J. P. Org. Lett. 2001, 3, 1829-1831 [Co]:
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(2001)
Org. Lett
, vol.3
, pp. 1829-1831
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Zhao, C.X.1
Duffey, M.O.2
Taylor, S.J.3
Morken, J.P.4
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18
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35549009016
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For intramolecular reductive-aldol reaction [Rh
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(j) Lumby, R. J. R.; Joensuu, P. M.; Lam, H. W. Org. Lett. 2007, 9, 4367-4370. For intramolecular reductive-aldol reaction [Rh]:
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(2007)
Org. Lett
, vol.9
, pp. 4367-4370
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Lumby, R.J.R.1
Joensuu, P.M.2
Lam, H.W.3
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21
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1842631430
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Co
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(m) Bocknack, B. M.; Wang, L.-C; Krische, M. J. Proc. Natl. Acad. Sci. U. S. A. 2004, 101, 5421-5424[Co]:
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(2004)
Proc. Natl. Acad. Sci. U. S. A
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, pp. 5421-5424
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Bocknack, B.M.1
Wang, L.-C.2
Krische, M.J.3
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22
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0034803441
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(n) Baik, T.-G.; Luis, A. L.; Wang, L.-C; Krische, M. J. J. Am. Chem. Soc. 2001, 123, 5112-5113.
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(2001)
J. Am. Chem. Soc
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, pp. 5112-5113
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Baik, T.-G.1
Luis, A.L.2
Wang, L.-C.3
Krische, M.J.4
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23
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0037077589
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(o) Wang, L.-C; Jang, H.-Y.; Roh, Y.; Lynch, V.; Schultz, A. J.; Wang, X.; Krische, M. J. J. Am. Chem. Soc. 2002, 124, 9448-9453.
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(2002)
J. Am. Chem. Soc
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Wang, L.-C.1
Jang, H.-Y.2
Roh, Y.3
Lynch, V.4
Schultz, A.J.5
Wang, X.6
Krische, M.J.7
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24
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33748616837
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Cu
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(p) Lam, H. W.; Joensuu, P. M.; Murray, G. J.; Fordyce, E. A. F.; Prieto, O.; Luebbers, T. Ore. Lett. 2006, 8, 3729-3732[Cu]:
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(2006)
Ore. Lett
, vol.8
, pp. 3729-3732
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Lam, H.W.1
Joensuu, P.M.2
Murray, G.J.3
Fordyce, E.A.F.4
Prieto, O.5
Luebbers, T.6
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25
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0032506682
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(q) Chiu, P.; Chen, B.; Cheng, K. F. Tetrahedron Lett. 1998, 39, 9229-9232.
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(1998)
Tetrahedron Lett
, vol.39
, pp. 9229-9232
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Chiu, P.1
Chen, B.2
Cheng, K.F.3
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26
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0000975755
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(r) Chiu, P.; Szeto, C P.; Geng, Z.; Cheng, K. F. Ore. Lett. 2001, 3, 1901-1903.
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(2001)
Ore. Lett
, vol.3
, pp. 1901-1903
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Chiu, P.1
Szeto, C.P.2
Geng, Z.3
Cheng, K.F.4
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27
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0035844674
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(s) Chiu, P.; Szeto, C. P.; Geng, Z.; Cheng, K. F. Tetrahedron Lett. 2001, 42, 4091-4093.
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(2001)
Tetrahedron Lett
, vol.42
, pp. 4091-4093
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Chiu, P.1
Szeto, C.P.2
Geng, Z.3
Cheng, K.F.4
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30
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1842637789
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(v) Agapiou, K.; Cauble, D. F.; Krische, M. J. J. Am. Chem. Soc. 2004, 126, 4528-4529.
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(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4528-4529
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Agapiou, K.1
Cauble, D.F.2
Krische, M.J.3
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32
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29444433067
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Lam, H. W.; Murray, G. J.; Firth, J. D. Ore. Lett. 2005, 7, 5743-5746. When the preparation of tins manuscript Lipshutz reported an enantioselective reductive-aldol reaction for the construction of cyclic compound:
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(x) Lam, H. W.; Murray, G. J.; Firth, J. D. Ore. Lett. 2005, 7, 5743-5746. When the preparation of tins manuscript Lipshutz reported an enantioselective reductive-aldol reaction for the construction of cyclic compound:
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33
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55549102693
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Chem. Soc, All references about reductive aldol reaction are summarized in the Supporting Information
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(y) Lipshutz, B. H.; Amorelli, B.; Unger, J. B. J. Am. Chem. Soc. 2008, 130, 14378-14379, All references about reductive aldol reaction are summarized in the Supporting Information.
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(2008)
J. Am
, vol.130
, pp. 14378-14379
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Lipshutz, B.H.1
Amorelli, B.2
Unger, J.B.3
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34
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33744913650
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In the same time, Shibasaki reported a similar catalytic system with low to moderate selectivities
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(a) Deschamp, J.; Chuzel, O.; Hannedouche, J.; Riant, O. Angew, Chem.. Int. Ed. 2006, 45, 1292-1297. In the same time, Shibasaki reported a similar catalytic system with low to moderate selectivities:
-
(2006)
Angew, Chem.. Int. Ed
, vol.45
, pp. 1292-1297
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Deschamp, J.1
Chuzel, O.2
Hannedouche, J.3
Riant, O.4
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35
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31444451603
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For studies on the influence of the TaniaPhos structure see
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(b) Zhao, D. B.; Oisaki, K.; Kanai, M.; Shibasaki, M. Tetrahedron Lett. 2006, 47, 1403-1407. For studies on the influence of the TaniaPhos structure see:
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 1403-1407
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Zhao, D.B.1
Oisaki, K.2
Kanai, M.3
Shibasaki, M.4
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36
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33750969372
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For catalytic asymmetric reductive-aldol of allenic esters to ketones see
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(c) Zhao, D.; Oisaki, K.; Kanai, M.; Shibasaki, M. J. Am. Chem. Soc. 2006, 128, 14440-14441. For catalytic asymmetric reductive-aldol of allenic esters to ketones see:
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 14440-14441
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Zhao, D.1
Oisaki, K.2
Kanai, M.3
Shibasaki, M.4
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37
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33744923178
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(d) Oisaki, K.; Zhao, D.; Kanai, M.; Shibasaki, M. J. Am. Chem. Soc. 2006, 128, 7164-7165.
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(2006)
J. Am. Chem. Soc
, vol.128
, pp. 7164-7165
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Oisaki, K.1
Zhao, D.2
Kanai, M.3
Shibasaki, M.4
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38
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33846137282
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Chuzel, O.; Deschamp, J.; Chausteur, C; Riant, O. Ore. Lett. 2006, 8, 5943-5946.
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(2006)
Ore. Lett
, vol.8
, pp. 5943-5946
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Chuzel, O.1
Deschamp, J.2
Chausteur, C.3
Riant, O.4
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39
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33847804804
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(a) Mukaiyama, T.; Banno, K.; Narasaka, K. J. Am. Chem. Soc. 1974, 96, 7503-7509.
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(1974)
J. Am. Chem. Soc
, vol.96
, pp. 7503-7509
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Mukaiyama, T.1
Banno, K.2
Narasaka, K.3
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40
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0037620632
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(b) Oisaki, K.; Suto, Y.; Kanai, M.; Shibasaki, M. J. Am. Chem. Soc. 2003, 125, 5644-5645.
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J. Am. Chem. Soc
, vol.125
, pp. 5644-5645
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Oisaki, K.1
Suto, Y.2
Kanai, M.3
Shibasaki, M.4
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41
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0000493922
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3.•2MeOH was prepared according to a literature procedure: Gulliver, D. J.; Levason, W.; Webster, M. Inore. Chim. Ada 1981, 52, 153-159.
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3.•2MeOH was prepared according to a literature procedure: Gulliver, D. J.; Levason, W.; Webster, M. Inore. Chim. Ada 1981, 52, 153-159.
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42
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0038537593
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The diketo-ester 2a is easily prepared in two-steps, starting from the commercially available 2-methyl-l, 3-cyclohexanedione. (a) Huddleston, R. R.; Krische, M. J. Ore. Lett. 2003, 5, 1143-1146.
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The diketo-ester 2a is easily prepared in two-steps, starting from the commercially available 2-methyl-l, 3-cyclohexanedione. (a) Huddleston, R. R.; Krische, M. J. Ore. Lett. 2003, 5, 1143-1146.
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43
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0036026242
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(b) Thiemann, T.; Umeno, K.; Wang, J.; Tabuchi, Y.; Arima, K.; Watanabe, M.; Tanaka, Y.; Gorohmaru, H.; Mataka, S. J. Chem. Soc. Perkin Trans. 1 2002, 2090-2110.
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J. Chem. Soc. Perkin Trans. 1
, pp. 2090-2110
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Thiemann, T.1
Umeno, K.2
Wang, J.3
Tabuchi, Y.4
Arima, K.5
Watanabe, M.6
Tanaka, Y.7
Gorohmaru, H.8
Mataka, S.9
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44
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64349094478
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Cis and trans nomenclature referred to the relation of the different substituents on the bicyclic junction
-
Cis and trans nomenclature referred to the relation of the different substituents on the bicyclic junction.
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45
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0037007673
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3) the configuration is S. Yamazaki, J.; Bedekar, A. V.; Watanabe, T.; Tanaka, K.; Watanabe, J.; Fuji, K. Tetrahedron Asymmetry 2002, 13, 729-734.
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3) the configuration is S. Yamazaki, J.; Bedekar, A. V.; Watanabe, T.; Tanaka, K.; Watanabe, J.; Fuji, K. Tetrahedron Asymmetry 2002, 13, 729-734.
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-
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46
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64349087741
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Ferrocenyl ligands like JosiPhos, WalPhos and MandyPhos were also tested but gave low selectivities
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Ferrocenyl ligands like JosiPhos, WalPhos and MandyPhos were also tested but gave low selectivities.
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47
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64349084312
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For the preparation of the Wieland-Miescher ketone, see
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For the preparation of the Wieland-Miescher ketone, see:
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-
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50
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0017386028
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(c) Welch, S. C; Hagan, C. P.; White, D. H.; Fleming, W. P.; Trotter, J. W. J. Am. Chem. Soc. 1977, 99, 549-556.
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Welch, S.C.1
Hagan, C.P.2
White, D.H.3
Fleming, W.P.4
Trotter, J.W.5
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52
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0034596452
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For some examples for the use of the Wieland-Miescher ketone in total synthesis, see
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(e) Bui, T.; Barbas, C. F., III Tetrahedron Lett. 2000, 41, 6951-6954. For some examples for the use of the Wieland-Miescher ketone in total synthesis, see:
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(2000)
Tetrahedron Lett
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Bui, T.1
Barbas III, C.F.2
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55
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0035966238
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(h) Ling, T.; Chowdhury, C; Kramer, B. A.; Vong, B. G.; Palladino, M. A.; Theodorakis, E. A. J. Ore. Chem. 2001, 66, 8843-8853.
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J. Ore. Chem
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Ling, T.1
Chowdhury, C.2
Kramer, B.A.3
Vong, B.G.4
Palladino, M.A.5
Theodorakis, E.A.6
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56
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1642569134
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(i) Ghosh, S.; Rivas, F.; Fischer, D.; Gonzalez, A.; Theodorakis, E. A. Ore. Lett. 2004, 6, 941-944.
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(2004)
Ore. Lett
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Ghosh, S.1
Rivas, F.2
Fischer, D.3
Gonzalez, A.4
Theodorakis, E.A.5
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57
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33746089158
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2 but the olefin was isolated with 30-40% yields. Katoh, T.; Mizumoto, S.; Fudesaka, M.; Takeo, M.; Kajimoto, T.; Node, M. Tetrahedron Asymmetry 2006, 17, 1655-1662.
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2 but the olefin was isolated with 30-40% yields. Katoh, T.; Mizumoto, S.; Fudesaka, M.; Takeo, M.; Kajimoto, T.; Node, M. Tetrahedron Asymmetry 2006, 17, 1655-1662.
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(a) Kingsbury, J. S.; Harrity, J. P. A.; Bonitatebus, P. J.; Hoveyda, A. H. J. Am. Chem. Soc. 1999, 121, 791-799.
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(b) Garber, S. B.; Kingsbury, J. S.; Gray, B. L.; Hoveyda, A. H. J. Am. Chem. Soc. 2000, 122, 8168-8179.
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(c) Cossy, J.; BouzBouz, S.; Hoveyda, A. H. J. Oreanomet. Chem. 2001, 634, 215-221.
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Cossy, J.1
BouzBouz, S.2
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61
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64349101745
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We observed a total conversion of 8 in presence of a large excess of phenylsilane.
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We observed a total conversion of 8 in presence of a large excess of phenylsilane.
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