-
1
-
-
33845471613
-
-
(a) Evans, D. A.; Ennis, M. D.; Le, T.; Mandel, N.; Mandel, G. J. Am. Chem. Soc. 1984, 106, 1154.
-
(1984)
J. Am. Chem. Soc
, vol.106
, pp. 1154
-
-
Evans, D.A.1
Ennis, M.D.2
Le, T.3
Mandel, N.4
Mandel, G.5
-
2
-
-
0025364262
-
-
(b) Evans, D. A.; Clark, J. S.; Metternich, R.; Novack, V. J.; Sheppard, G. S. J. Am. Chem. Soc. 1990, 112, 866.
-
(1990)
J. Am. Chem. Soc
, vol.112
, pp. 866
-
-
Evans, D.A.1
Clark, J.S.2
Metternich, R.3
Novack, V.J.4
Sheppard, G.S.5
-
3
-
-
0026005895
-
-
For selected examples, see: a
-
For selected examples, see: (a) Evans, D. A.; Polniaszek, R. P.; DeVries, K. M.; Guinn, D. E.; Mathre, D. J. J. Am. Chem. Soc. 1991, 113, 7613.
-
(1991)
J. Am. Chem. Soc
, vol.113
, pp. 7613
-
-
Evans, D.A.1
Polniaszek, R.P.2
DeVries, K.M.3
Guinn, D.E.4
Mathre, D.J.5
-
4
-
-
0034679519
-
-
(b) Evans, D. A.; Cee, V. J.; Smith, T. E.; Fitch, D. M.; Cho, P. S. Angew. Chem., Int. Ed. 2000, 39, 2533.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 2533
-
-
Evans, D.A.1
Cee, V.J.2
Smith, T.E.3
Fitch, D.M.4
Cho, P.S.5
-
5
-
-
0034684178
-
-
(c) Evans, D. A.; Fitch, D. M.; Smith, T. E.; Cee, V. J. J. Am. Chem. Soc. 2000, 122, 10033.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 10033
-
-
Evans, D.A.1
Fitch, D.M.2
Smith, T.E.3
Cee, V.J.4
-
6
-
-
33846495712
-
-
(d) Evans, D. A.; Nagorny, P.; McRae, K. J.; Reynolds, D. J.; Sonntag, L.-S.; Vounatsos, F.; Xu, R. Angew. Chem., Int. Ed. 2007, 46, 537.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 537
-
-
Evans, D.A.1
Nagorny, P.2
McRae, K.J.3
Reynolds, D.J.4
Sonntag, L.-S.5
Vounatsos, F.6
Xu, R.7
-
7
-
-
0023891875
-
-
(e) Nakata, T.; Fukui, M.; Oishi, T. Tetrahedron Lett. 1988, 29, 2219.
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 2219
-
-
Nakata, T.1
Fukui, M.2
Oishi, T.3
-
8
-
-
0037165675
-
-
(f) Paquette, L. A.; Duan, M.; Konetzki, I.; Kempmann, C. J. Am. Chem. Soc. 2002, 124, 4257.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 4257
-
-
Paquette, L.A.1
Duan, M.2
Konetzki, I.3
Kempmann, C.4
-
9
-
-
33746285272
-
-
(g) Lister, T.; Perkins, M. V. Angew. Chem., Int. Ed. 2006, 45, 2560.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 2560
-
-
Lister, T.1
Perkins, M.V.2
-
11
-
-
0001469676
-
-
(b) Padwa, A.; Hornbuckle, S. F.; Zhang, Z.; Zhi, Li. J. Org. Chem. 1990, 55, 5297.
-
(1990)
J. Org. Chem
, vol.55
, pp. 5297
-
-
Padwa, A.1
Hornbuckle, S.F.2
Zhang, Z.3
Zhi, L.4
-
12
-
-
0010471544
-
-
(c) López-Herrera, F. J.; Valpuesta-Fernández, M.; Garía-Claros, S. Tetrahedron 1990, 46, 7165.
-
(1990)
Tetrahedron
, vol.46
, pp. 7165
-
-
López-Herrera, F.J.1
Valpuesta-Fernández, M.2
Garía-Claros, S.3
-
13
-
-
37049083721
-
-
For very limited examples, see: a
-
For very limited examples, see: (a) Jephcote, V. J.; Jowett, I. C.; John, D. I.; Edwards, P. D.; Luk, K.; Slawin, A. M.; Williams, D. J. J. Chem. Soc., Perkin Trans. 1 1986, 2187.
-
(1986)
J. Chem. Soc., Perkin Trans. 1
, pp. 2187
-
-
Jephcote, V.J.1
Jowett, I.C.2
John, D.I.3
Edwards, P.D.4
Luk, K.5
Slawin, A.M.6
Williams, D.J.7
-
14
-
-
45649084754
-
-
(b) Murata, H.; Ishitani, H.; Iwamoto, M. Tetrahedron Lett. 2008, 49, 4788.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 4788
-
-
Murata, H.1
Ishitani, H.2
Iwamoto, M.3
-
15
-
-
0000252759
-
-
Use of arylaldehydes tends to give the aryl transfer products dominantly; see: a
-
Use of arylaldehydes tends to give the aryl transfer products dominantly; see: (a) Mahmood, S. J.; Hossain, M. M. J. Org. Chem. 1998, 63, 3333.
-
(1998)
J. Org. Chem
, vol.63
, pp. 3333
-
-
Mahmood, S.J.1
Hossain, M.M.2
-
16
-
-
0033516531
-
-
(b) Kanemasa, S.; Kanai, T.; Araki, T.; Wada, E. Tetrahedron Lett. 1999, 40, 5055.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 5055
-
-
Kanemasa, S.1
Kanai, T.2
Araki, T.3
Wada, E.4
-
17
-
-
68849087264
-
-
Cufini, M.; Epigano, F.; Marcotullio, M. C.; Rosati, O. Eur. J. Org. Chem. 2002, 1562.
-
(2002)
Eur. J. Org. Chem
, pp. 1562
-
-
Cufini, M.1
Epigano, F.2
Marcotullio, M.C.3
Rosati, O.4
-
18
-
-
36849006510
-
-
(a) Hashimoto, T.; Naganawa, Y.; Kano, T.; Maruoka, K. Chem. Commun. 2007, 5143.
-
(2007)
Chem. Commun
, pp. 5143
-
-
Hashimoto, T.1
Naganawa, Y.2
Kano, T.3
Maruoka, K.4
-
19
-
-
39749121974
-
-
(b) Hashimoto, T.; Naganawa, Y.; Maruoka, K. J. Am. Chem. Soc. 2008, 130, 2434.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 2434
-
-
Hashimoto, T.1
Naganawa, Y.2
Maruoka, K.3
-
20
-
-
69949118503
-
-
(c) Hashimoto, T.; Naganawa, Y.; Maruoka, K. J. Am. Chem. Soc. 2009, 130, 6614.
-
(2009)
J. Am. Chem. Soc
, vol.130
, pp. 6614
-
-
Hashimoto, T.1
Naganawa, Y.2
Maruoka, K.3
-
21
-
-
27544467423
-
-
Ma, M.; Peng, L.; Li, C.; Zhang, X.; Wang, J. J. Am. Chem. Soc. 2005, 127, 15016.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 15016
-
-
Ma, M.1
Peng, L.2
Li, C.3
Zhang, X.4
Wang, J.5
-
23
-
-
0029029880
-
-
Moreno-Mañas, M.; Sebastián, R. M.; Vallribera, A.; Molins, E. Tetrahedron 1995, 51, 10795.
-
(1995)
Tetrahedron
, vol.51
, pp. 10795
-
-
Moreno-Mañas, M.1
Sebastián, R.M.2
Vallribera, A.3
Molins, E.4
-
24
-
-
68849091098
-
-
1H NMR, which could be separated by column chromatography on silica gel.
-
1H NMR, which could be separated by column chromatography on silica gel.
-
-
-
-
25
-
-
68849124503
-
-
For the determination of the relative configuration and the discussion on the stereochemical outcome, see Supporting Information
-
For the determination of the relative configuration and the discussion on the stereochemical outcome, see Supporting Information.
-
-
-
-
26
-
-
68849130714
-
-
2 for 3 days led to the predominant formation of the opposite diastereomer (dr = 1:3).
-
2 for 3 days led to the predominant formation of the opposite diastereomer (dr = 1:3).
-
-
-
-
27
-
-
38349184575
-
-
For recent examples of Roskamp reaction with α-chiral aldehydes, see: a
-
For recent examples of Roskamp reaction with α-chiral aldehydes, see: (a) Toueg, J.; Prunet, J. Org. Lett. 2008, 10, 45.
-
(2008)
Org. Lett
, vol.10
, pp. 45
-
-
Toueg, J.1
Prunet, J.2
-
28
-
-
37549068490
-
-
(b) Schweizer, E.; Gaich, T.; Brecker, L.; Mulzer, J. Synthesis 2007, 3807.
-
(2007)
Synthesis
, pp. 3807
-
-
Schweizer, E.1
Gaich, T.2
Brecker, L.3
Mulzer, J.4
-
30
-
-
0029018579
-
-
(a) Taniguchi, M.; Oshima, K.; Utimoto, K. Bull. Chem. Soc. Jpn. 1995, 68, 645.
-
(1995)
Bull. Chem. Soc. Jpn
, vol.68
, pp. 645
-
-
Taniguchi, M.1
Oshima, K.2
Utimoto, K.3
-
31
-
-
0035959473
-
-
(b) Bartoli, G.; Bosco, M.; Marcantoni, E.; Massaccesi, M.; Rinaldi, S.; Sambri, L. Tetrahedron Lett. 2001, 42, 6093.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 6093
-
-
Bartoli, G.1
Bosco, M.2
Marcantoni, E.3
Massaccesi, M.4
Rinaldi, S.5
Sambri, L.6
-
32
-
-
68849116078
-
-
Zinc borohydride reduction and nucleophilic addition of MeMgI also proceeded with high diasteroselectivity. See Supporting Information
-
Zinc borohydride reduction and nucleophilic addition of MeMgI also proceeded with high diasteroselectivity. See Supporting Information.
-
-
-
-
33
-
-
0001597804
-
-
(a) Evans, D. A.; Britton, T. C.; Ellman, J. A. Tetrahedron Lett. 1987, 28, 6141.
-
(1987)
Tetrahedron Lett
, vol.28
, pp. 6141
-
-
Evans, D.A.1
Britton, T.C.2
Ellman, J.A.3
-
34
-
-
0000133961
-
-
(b) Oppolzer, W.; Blagg, J.; Rodriguez, I.; Walther, E. J. Am. Chem. Soc. 1990, 112, 2767.
-
(1990)
J. Am. Chem. Soc
, vol.112
, pp. 2767
-
-
Oppolzer, W.1
Blagg, J.2
Rodriguez, I.3
Walther, E.4
-
36
-
-
33845554892
-
-
Evans, D. A.; Ennis, M. D.; Mathre, D. J. J. Am. Chem. Soc. 1982, 104, 1737.
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 1737
-
-
Evans, D.A.1
Ennis, M.D.2
Mathre, D.J.3
-
37
-
-
0033591141
-
-
For the synthetic applications of β-lactones, see
-
For the synthetic applications of β-lactones, see: Yang, H. W.; Romo, D. Tetrahedron 1999, 55, 6403.
-
(1999)
Tetrahedron
, vol.55
, pp. 6403
-
-
Yang, H.W.1
Romo, D.2
|