-
1
-
-
33749838015
-
-
Product selectivity control is an important issue in organic synthesis, for recent reviews, see: a
-
Product selectivity control is an important issue in organic synthesis, for recent reviews, see: a) J.-J. Brunet, R. Poli, Chemtracts 2004, 17, 381;
-
(2004)
Chemtracts
, vol.17
, pp. 381
-
-
Brunet, J.-J.1
Poli, R.2
-
2
-
-
13244254111
-
-
b) M. Beller, J. Seayad, A. Tillack, H. Jiao, Angew. Chem. 2004, 116, 3448;
-
(2004)
Angew. Chem
, vol.116
, pp. 3448
-
-
Beller, M.1
Seayad, J.2
Tillack, A.3
Jiao, H.4
-
7
-
-
21244479265
-
-
for selected examples since 2005, see: e
-
for selected examples since 2005, see: e) S. Kamijo, C. Kanazawa, Y. Yamamoto, J. Am. Chem. Soc. 2005, 127, 9260;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 9260
-
-
Kamijo, S.1
Kanazawa, C.2
Yamamoto, Y.3
-
8
-
-
33645305026
-
-
f) N. P. Grimster, C. Gauntlett, C. R. A. Godfrey, M. J. Gaunt, Angew. Chem. 2005, 117, 3185;
-
(2005)
Angew. Chem
, vol.117
, pp. 3185
-
-
Grimster, N.P.1
Gauntlett, C.2
Godfrey, C.R.A.3
Gaunt, M.J.4
-
12
-
-
33644658464
-
-
i) E. M. Beck, N. P. Grimster, R. Hatley, M. J. Gaunt, J. Am. Chem. Soc. 2006, 128, 2528;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 2528
-
-
Beck, E.M.1
Grimster, N.P.2
Hatley, R.3
Gaunt, M.J.4
-
13
-
-
33646594410
-
-
j) R. Shintani, W.-L. Duan, T. Hayashi, J. Am. Chem. Soc. 2006, 128, 5268;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 5268
-
-
Shintani, R.1
Duan, W.-L.2
Hayashi, T.3
-
14
-
-
33845190114
-
-
k) S. Brandau, E. Maerten, K. A. Jørgensen, J. Am. Chem. Soc. 2006, 128, 14986;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 14986
-
-
Brandau, S.1
Maerten, E.2
Jørgensen, K.A.3
-
15
-
-
41449090176
-
-
l) L.-C. Campeau, M. Bertrand-Laperle, J. P. Leclerc, E. Villemure, S. Gorelsky, K. Fagnou, J. Am. Chem. Soc. 2008, 130, 3276.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 3276
-
-
Campeau, L.-C.1
Bertrand-Laperle, M.2
Leclerc, J.P.3
Villemure, E.4
Gorelsky, S.5
Fagnou, K.6
-
16
-
-
58549106270
-
-
Many chemists have contributed to this field, but only 1-2 typical examples were selected here from each group, see: a G. Dyker, D. Hildebrandt, J. Liu, K. Merz, Angew. Chem. 2003, 115, 4536;
-
Many chemists have contributed to this field, but only 1-2 typical examples were selected here from each group, see: a) G. Dyker, D. Hildebrandt, J. Liu, K. Merz, Angew. Chem. 2003, 115, 4536;
-
-
-
-
18
-
-
33748945708
-
-
S
-
b) N. Asao, K. Iso, S. Yudha S, Org. Lett. 2006, 8, 4149;
-
(2006)
Org. Lett
, vol.8
, pp. 4149
-
-
Asao, N.1
Iso, K.2
Yudha, S.3
-
20
-
-
33646259513
-
-
d) D. Yue, N. Della Ca, R. C. Larock, J. Org. Chem. 2006, 71, 3381;
-
(2006)
J. Org. Chem
, vol.71
, pp. 3381
-
-
Yue, D.1
Della Ca, N.2
Larock, R.C.3
-
22
-
-
36849062645
-
-
f) Q. Ding, B. Wang, J. Wu, Org. Lett. 2007, 9, 4959;
-
(2007)
Org. Lett
, vol.9
, pp. 4959
-
-
Ding, Q.1
Wang, B.2
Wu, J.3
-
24
-
-
34250169005
-
-
h) S. Obika, H. Kono, Y. Yasui, R. Yanada, Y. Takemoto, J. Org. Chem. 2007, 72, 4462;
-
(2007)
J. Org. Chem
, vol.72
, pp. 4462
-
-
Obika, S.1
Kono, H.2
Yasui, Y.3
Yanada, R.4
Takemoto, Y.5
-
25
-
-
58549104254
-
-
imine analogue, see: i N. Asao, S. Y. S. T. Nogami, Y. Yamamoto, Angew. Chem. 2005, 117, 5662;
-
imine analogue, see: i) N. Asao, S. Y. S. T. Nogami, Y. Yamamoto, Angew. Chem. 2005, 117, 5662;
-
-
-
-
27
-
-
0037028560
-
-
a) N. Asao, T. Nogami, K. Takahashi, Y. Yamamoto, J. Am. Chem. Soc. 2002, 124, 764;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 764
-
-
Asao, N.1
Nogami, T.2
Takahashi, K.3
Yamamoto, Y.4
-
28
-
-
0037202125
-
-
b) N. Asao, K. Takahashi, S. Lee, T. Kasahara, Y. Yamamoto, J. Am. Chem. Soc. 2002, 124, 12650;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 12650
-
-
Asao, N.1
Takahashi, K.2
Lee, S.3
Kasahara, T.4
Yamamoto, Y.5
-
29
-
-
0042734705
-
-
c) N. Asao, T. Nogami, S. Lee, Y. Yamamoto, J. Am. Chem. Soc. 2003, 125, 10921;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 10921
-
-
Asao, N.1
Nogami, T.2
Lee, S.3
Yamamoto, Y.4
-
30
-
-
0141654566
-
-
d) N. Asao, T. Kasahara, Y. Yamamoto, Angew. Chem. 2003, 115, 3628;
-
(2003)
Angew. Chem
, vol.115
, pp. 3628
-
-
Asao, N.1
Kasahara, T.2
Yamamoto, Y.3
-
32
-
-
2942682670
-
-
e) N. Asao, H. Aikawa, Y. Yamamoto, J. Am. Chem. Soc. 2004, 126, 7548.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 7548
-
-
Asao, N.1
Aikawa, H.2
Yamamoto, Y.3
-
33
-
-
0042367613
-
-
a) J. Barluenga, H. Vázquez-Villa, A. Ballesteros, J. M. González, J. Am. Chem. Soc. 2003, 125, 9028;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 9028
-
-
Barluenga, J.1
Vázquez-Villa, H.2
Ballesteros, A.3
González, J.M.4
-
34
-
-
0344082894
-
-
b) J. Barluenga, H. Vázquez-Villa, A. Ballesteros, J. M. González, Org. Lett. 2003, 5, 4121;
-
(2003)
Org. Lett
, vol.5
, pp. 4121
-
-
Barluenga, J.1
Vázquez-Villa, H.2
Ballesteros, A.3
González, J.M.4
-
35
-
-
33746806249
-
-
c) J. Barluenga, H. Vázquez-Villa, I. Merino, A. Ballesteros, J. M. González, Chem. Eur. J. 2006, 12, 5790.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 5790
-
-
Barluenga, J.1
Vázquez-Villa, H.2
Merino, I.3
Ballesteros, A.4
González, J.M.5
-
36
-
-
0035922318
-
-
a) Q. Huang, J. A. Hunter, R. C. Larock, Org. Lett. 2001, 3, 2973;
-
(2001)
Org. Lett
, vol.3
, pp. 2973
-
-
Huang, Q.1
Hunter, J.A.2
Larock, R.C.3
-
38
-
-
0037123652
-
-
c) Q. Huang, J. A. Hunter, R. C. Larock, J. Org. Chem. 2002, 67, 3437;
-
(2002)
J. Org. Chem
, vol.67
, pp. 3437
-
-
Huang, Q.1
Hunter, J.A.2
Larock, R.C.3
-
42
-
-
58549108909
-
-
1,2-Allenes, 1,3-dienes and 4H-pyrans could be produced selectively by reacting electron-deficient 1,3-conjugated enynes with different nucleophiles, see: X. Yu, H. Ren, Y. Xiao, J. Zhang, Chem. Eur. J. 2008, ASAP.
-
1,2-Allenes, 1,3-dienes and 4H-pyrans could be produced selectively by reacting electron-deficient 1,3-conjugated enynes with different nucleophiles, see: X. Yu, H. Ren, Y. Xiao, J. Zhang, Chem. Eur. J. 2008, ASAP.
-
-
-
-
43
-
-
58549093651
-
-
During our study of this PSCR, Ag(I)-catalyzed cyclization of ortho-alkynylaryl aldehyde oxime leading to isoquinoline N-oxides was published by Seunghoon Shin, see: H.-S. Yeom, S. Kim, S. Shin, Synlett 2008, 924;
-
During our study of this PSCR, Ag(I)-catalyzed cyclization of ortho-alkynylaryl aldehyde oxime leading to isoquinoline N-oxides was published by Seunghoon Shin, see: H.-S. Yeom, S. Kim, S. Shin, Synlett 2008, 924;
-
-
-
-
44
-
-
53849138392
-
-
for an electrophiles-mediated version of this cyclization to afford the corresponding 4-halide-isoquinoline N-oxides, see: Q. Ding, J. Wu, Adv. Synth. Catal. 2008, 350, 1850.
-
for an electrophiles-mediated version of this cyclization to afford the corresponding 4-halide-isoquinoline N-oxides, see: Q. Ding, J. Wu, Adv. Synth. Catal. 2008, 350, 1850.
-
-
-
-
45
-
-
58549099389
-
-
Functionalized isoquinolines are an important class of heterocylic compounds with many bioactive activities, see: a The Chemistry of Heterocyclic Compounds: Isoqinolines, Eds, G. M. Coppola, H. F. Schuster, John Wiley & Sons, New York, 1981, 38, Part 3;
-
Functionalized isoquinolines are an important class of heterocylic compounds with many bioactive activities, see: a) The Chemistry of Heterocyclic Compounds: Isoqinolines, (Eds.: G. M. Coppola, H. F. Schuster), John Wiley & Sons, New York, 1981, Vol. 38, Part 3;
-
-
-
-
46
-
-
0033798476
-
-
b) M. Croisy-Delcey, A. Croisy, D. Carrez, C. Huel, A. Chiaroni, P. Durot, E. Bisagni, L. Jin, G. Leclerq, Bioorg. Med. Chem. 2000, 8, 2629;
-
(2000)
Bioorg. Med. Chem
, vol.8
, pp. 2629
-
-
Croisy-Delcey, M.1
Croisy, A.2
Carrez, D.3
Huel, C.4
Chiaroni, A.5
Durot, P.6
Bisagni, E.7
Jin, L.8
Leclerq, G.9
-
47
-
-
58549093098
-
-
[5] ;
-
[5] ;
-
-
-
-
48
-
-
0141855014
-
-
d) S. G. Lim, J. H. Lee, C. W. Moon, J.-B. Hong, C. H. Jun, Org. Lett. 2003, 5 2759;
-
(2003)
Org. Lett
, vol.5
, pp. 2759
-
-
Lim, S.G.1
Lee, J.H.2
Moon, C.W.3
Hong, J.-B.4
Jun, C.H.5
-
49
-
-
28044446342
-
-
e) T. Konno, J. Chae, T. Miyabe, T. Ishihara, J. Org. Chem. 2005, 70, 10172;
-
(2005)
J. Org. Chem
, vol.70
, pp. 10172
-
-
Konno, T.1
Chae, J.2
Miyabe, T.3
Ishihara, T.4
-
51
-
-
33747210404
-
-
g) R. Alonso, P. J. Campos, B. García, M. A. Rodríguez, Org. Lett. 2006, 8, 3521;
-
(2006)
Org. Lett
, vol.8
, pp. 3521
-
-
Alonso, R.1
Campos, P.J.2
García, B.3
Rodríguez, M.A.4
-
52
-
-
36849026774
-
-
h) D. Fischer, H. Tomeba, N. K. Pahadi, N. T. Patil, Y. Yamamoto, Angew. Chem. 2007, 119, 4848;
-
(2007)
Angew. Chem
, vol.119
, pp. 4848
-
-
Fischer, D.1
Tomeba, H.2
Pahadi, N.K.3
Patil, N.T.4
Yamamoto, Y.5
-
54
-
-
34250895132
-
-
Methods for synthesis of isoquinolin-1(2H)-ones, see: a) V. R. Batchu, D. K. Barange, D. Kumar, B. R. Sreekanth, K. Vyas, E. A. Reddy, M. Pal, Chem. Commun. 2007, 1966;
-
Methods for synthesis of isoquinolin-1(2H)-ones, see: a) V. R. Batchu, D. K. Barange, D. Kumar, B. R. Sreekanth, K. Vyas, E. A. Reddy, M. Pal, Chem. Commun. 2007, 1966;
-
-
-
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