-
4
-
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33847804804
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For aldol reactions, see: a
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Mukaiyama, T.1
Banno, K.2
Narasaka, K.3
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6
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0000858703
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(c) Kobayashi, S.; Uchiro, T.; Fujishita, Y.; Shiina, I.; Mukaiyama, T. J. Am. Chem. Soc. 1991, 113, 4247.
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Kobayashi, S.1
Uchiro, T.2
Fujishita, Y.3
Shiina, I.4
Mukaiyama, T.5
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7
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0020507552
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For Mannich-type reactions, see: d
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For Mannich-type reactions, see: (d) Ikeda, K.; Achiwa, K.; Sekiya, M. Tetrahedron Lett. 1983, 24, 4707.
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Ikeda, K.1
Achiwa, K.2
Sekiya, M.3
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9
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0030788354
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(f) Ishitani, H.; Ueno, M.; Kobayashi, S. J. Am. Chem. Soc. 1997, 119, 7153.
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Ishitani, H.1
Ueno, M.2
Kobayashi, S.3
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10
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0002573501
-
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For 1, 4-addition, see: g
-
For 1, 4-addition, see: (g) Narasaka, K.; Soai, K.; Mukaiyama, T. Chem. Lett. 1974, 1223.
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(1974)
Chem. Lett.
, pp. 1223
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Narasaka, K.1
Soai, K.2
Mukaiyama, T.3
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11
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0000776965
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(h) Narasaka, K.; Soai, K.; Aikawa, Y.; Mukaiyama, T. Bull. Chem. Soc. Jpn. 1976, 49, 779.
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Narasaka, K.1
Soai, K.2
Aikawa, Y.3
Mukaiyama, T.4
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13
-
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0005696762
-
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Also see the following review: j
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Also see the following review: (j) Kobayashi, S.; Manabe, K.; Ishitani, H.; Matsuo, J.-i. Sci. Synth. 2002, 4, 317-369.
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Kobayashi, S.1
Manabe, K.2
Ishitani, H.3
Matsuo, J.-I.4
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14
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33947300284
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House, H. O.; Czuba, L. J.; Gall, M.; Olmstead, H. D. J. Org. Chem. 1969, 34, 2324.
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House, H.O.1
Czuba, L.J.2
Gall, M.3
Olmstead, H.D.4
-
15
-
-
0035926083
-
-
For examples of catalytic direct-type addition of ester-equivalent donors, see: a
-
For examples of catalytic direct-type addition of ester-equivalent donors, see: (a) Bunlaksananusorn, T.; Rodriguez, A. L.; Knochel, P. Chem. Commun. 2001, 745.
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Bunlaksananusorn, T.1
Rodriguez, A.L.2
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16
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6444227416
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(b) Kumagai, N.; Matsunaga, S.; Shibasaki, M. J. Am. Chem. Soc. 2004, 126, 13632.
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Kumagai, N.1
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18
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34547803869
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(b) Morimoto, H.; Lu, G.; Aoyama, N.; Matsunaga, S.; Shibasaki, M. J. Am. Chem. Soc. 2007, 129, 9588.
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Morimoto, H.1
Lu, G.2
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Shibasaki, M.5
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19
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70349538846
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(c) Matsubara, R.; Berthiol, F.; Nguyen, H. V.; Kobayashi, S. Bull. Chem. Soc. Jpn. 2009, 82, 1083.
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Matsubara, R.1
Berthiol, F.2
Nguyen, H.V.3
Kobayashi, S.4
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21
-
-
79951472073
-
-
reaction of the Ts inline derived from 3-phenylpropanal with la was not successful
-
The reaction of the Ts inline derived from 3-phenylpropanal with la was not successful.
-
-
-
-
22
-
-
79951488808
-
-
3 gave lower yields 50-75%. The anti/syn ratio was ∼6/1 in all cases
-
3 gave lower yields (50-75%). The anti/syn ratio was ∼6/1 in all cases.
-
-
-
-
23
-
-
0347717646
-
-
Mancheno, O. G.; Arrayás, R. G.; Carretero, J. C. J. Am. Chem. Soc. 2004, 126, 456.
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Mancheno, O.G.1
Arrayás, R.G.2
Carretero, J.C.3
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24
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0001209391
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Ferraris, D.; Young, B.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 1998, 120, 4548.
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Ferraris, D.1
Young, B.2
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Lectka, T.4
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25
-
-
33746649077
-
-
(a) Nagao, Y.; Miyamoto, S.; Miyamoto, M.; Takeshige, H.; Hayashi, K.; Sano, S.; Shiro, M.; Yamaguchi, K.; Sei, Y. J. Am. Chem. Soc. 2006, 128, 9722.
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Nagao, Y.1
Miyamoto, S.2
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Takeshige, H.4
Hayashi, K.5
Sano, S.6
Shiro, M.7
Yamaguchi, K.8
Sei, Y.9
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26
-
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0007315038
-
-
Also see: b
-
Also see: (b) Djuri, S. W. J. Org. Chem. 1984, 49, 1311.
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-
-
Djuri, S.W.1
-
29
-
-
79951473299
-
-
The preparation of the corresponding TIPS enolate failed the C-enolate was formed predominantly LDA/TIPSC1
-
The preparation of the corresponding TIPS enolate failed [the C-enolate was formed predominantly (LDA/TIPSC1)].
-
-
-
-
30
-
-
0037120156
-
-
For example, see
-
For example, see: Kobayashi, S.; Kobayashi, J.; Ishitani, H.; Ueno, M. Chem.-Eur. J. 2002, 8, 4185.
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Kobayashi, S.1
Kobayashi, J.2
Ishitani, H.3
Ueno, M.4
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31
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0000699983
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Jacobsen, E. N., Pfaltz, A, Yamamoto, H., Eds.; Springer-Verlag: Berlin
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Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A, Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; p 997.
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Carreira, E.M.1
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