-
1
-
-
0001586671
-
Friedel-Crafts alkylations
-
Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
-
For a review of the Friedel-Crafts reactions see: Olah, G. A.; Krishnamurti, R.; Prakash, G. K. S. Friedel-Crafts Alkylations. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 3, pp 293-339.
-
(1991)
Comprehensive Organic Synthesis
, vol.3
, pp. 293-339
-
-
Olah, G.A.1
Krishnamurti, R.2
Prakash, G.K.S.3
-
2
-
-
0141892801
-
-
For examples of natural products which are relevant to the formed stereocenter, see cycloaplysinopsin: (a) Mancini, I.; Guella, G.; Zibrowius, H.; Pietra, F. Tetrahedron 2003, 59, 8757-8762.
-
(2003)
Tetrahedron
, vol.59
, pp. 8757-8762
-
-
Mancini, I.1
Guella, G.2
Zibrowius, H.3
Pietra, F.4
-
3
-
-
2042419021
-
-
10,11-Dimethoxynareline: (b) Kam, T.; Choo, Y. J. Nat. Prod. 2004, 67, 547-552.
-
(2004)
J. Nat. Prod.
, vol.67
, pp. 547-552
-
-
Kam, T.1
Choo, Y.2
-
5
-
-
0031733197
-
-
(d) Huber, U.; Moore, R. E.; Patterson, G. M. L. J. Nat. Prod. 1998, 61, 1304-1306.
-
(1998)
J. Nat. Prod.
, vol.61
, pp. 1304-1306
-
-
Huber, U.1
Moore, R.E.2
Patterson, G.M.L.3
-
6
-
-
0037147770
-
-
For examples of potential medicinal agents relevant to the formed stereocenter, see: (a) Rawson, D. J.; Dack, K. N.; Dickinson, R. P.; James, K. Biorg. Med. Chem. Lett. 2002, 12, 125-128.
-
(2002)
Biorg. Med. Chem. Lett.
, vol.12
, pp. 125-128
-
-
Rawson, D.J.1
Dack, K.N.2
Dickinson, R.P.3
James, K.4
-
8
-
-
1642619398
-
-
Chang-Fong, J.; Rangisetty, J. B.; Dukat, M.; Setola, V.; Raffay, T.; Roth, B.; Glennon, R. Biorg. Med. Chem. Lett. 2004, 14, 1961-1964.
-
(2004)
Biorg. Med. Chem. Lett.
, vol.14
, pp. 1961-1964
-
-
Chang-Fong, J.1
Rangisetty, J.B.2
Dukat, M.3
Setola, V.4
Raffay, T.5
Roth, B.6
Glennon, R.7
-
9
-
-
0035825178
-
-
For Cu(II)-catalyzed additions of aromatic systems to α,β-unsaturated α-keto esters, see: (a) Jensen, K. B.; Thorbauge, J.; Hazell, R. G.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2001, 40, 160-163.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 160-163
-
-
Jensen, K.B.1
Thorbauge, J.2
Hazell, R.G.3
Jørgensen, K.A.4
-
10
-
-
0034807741
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-
For additions of electron-rich aromatics and indoles to α,β-unsaturated aldehydes catalyzed by chiral secondary amines, see: (b) Paras, N. A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2001, 123, 4370-4371.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 4370-4371
-
-
Paras, N.A.1
MacMillan, D.W.C.2
-
12
-
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1242352444
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For Cu-(II)-catalyzed additions of indoles to alkylidene malonates, see: (d) Zhou, J.; Ye, M.-C.; Huang, Z.-Z.; Tang, Y. J. Org. Chem. 2004, 69, 1309-1320.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 1309-1320
-
-
Zhou, J.1
Ye, M.-C.2
Huang, Z.-Z.3
Tang, Y.4
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13
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16244408623
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For Cu(II)-catalyzed additions of indoles and pyrroles to α′-hydroxy enones, see: (e) Palomo, C.; Oiarbide, M.; Kardak, B. G.; Garcia, J. M.; Linden, A. J. Am. Chem. Soc. 2005, 127, 4154-4155.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 4154-4155
-
-
Palomo, C.1
Oiarbide, M.2
Kardak, B.G.3
Garcia, J.M.4
Linden, A.5
-
15
-
-
0042233997
-
-
Evans, D. A.; Scheidt, K. A. Fandrick, K. R.; Lam, H. W.; Wu, J. J. Am. Chem. Soc. 2003, 125, 10780-10781.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10780-10781
-
-
Evans, D.A.1
Scheidt, K.A.2
Fandrick, K.R.3
Lam, H.W.4
Wu, J.5
-
16
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0030803772
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For the transformation of 2-acyl benzimidazoles to esters, amides, β-diketones, and β-ketoesters, see: (a) Miyashita, A.; Suzuki, Y.; Nagasaki, I.; Ishiguro, C.; Iwamoto, K.-I.; Higashino, T. Chem. Pharm. Bull. 1997, 45, 1254-1258.
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 1254-1258
-
-
Miyashita, A.1
Suzuki, Y.2
Nagasaki, I.3
Ishiguro, C.4
Iwamoto, K.-I.5
Higashino, T.6
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17
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85011188491
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For the transformation of 2-acyl imidazoles to ketones, β-diketones, β-ketoesters, and aldehydes, see: (b) Ohta, S.; Hayakawa, S.; Nishimura, K.; Okamoto, M. Chem. Pharm. Bull. 1987, 35, 1058-1069.
-
(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 1058-1069
-
-
Ohta, S.1
Hayakawa, S.2
Nishimura, K.3
Okamoto, M.4
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18
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21244441108
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note
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All substrates explored showed increased product enantioselection with decreased catalyst loading.
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19
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0035814327
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Evans, D. A.; Sweeney, Z. K.; Rovis, T.; Tedrow, J. S. J. Am. Chem. Soc. 2001, 123, 12095-12096.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 12095-12096
-
-
Evans, D.A.1
Sweeney, Z.K.2
Rovis, T.3
Tedrow, J.S.4
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