-
1
-
-
0003467672
-
-
6 th ed. (Eds.: M. B. Smith, J. March), Wiley, New York, pp
-
March's Advanced Organic Chemistry: Reactions Mechanisms and Structure, 6 th ed., (Eds.: M. B. Smith, J. March,), Wiley, New York, 2007, pp. 61-63
-
(2007)
March's Advanced Organic Chemistry: Reactions Mechanisms and Structure
, pp. 61-63
-
-
-
2
-
-
79953218908
-
-
7 th ed. (Eds.: S. Kiselica, E. Bitter), Thomson, Belmont, pp
-
J. McMurry, Organic Chemistry, 7 th ed., (Eds.: S. Kiselica, E. Bitter,), Thomson, Belmont, 2008, pp. 946-948
-
(2008)
Organic Chemistry
, pp. 946-948
-
-
McMurry, J.1
-
3
-
-
79953198083
-
-
5 th ed. (Eds.: J. A. Joule, K. Mills), Wiley, New York, pp
-
Heterocyclic Chemistry, 5 th ed., (Eds.: J. A. Joule, K. Mills,), Wiley, New York, 2010, pp. 9-10.
-
(2010)
Heterocyclic Chemistry
, pp. 9-10
-
-
-
4
-
-
77956392641
-
-
in (Eds.: G. Jones, C. A. Ramsden), Elsevier, Oxford, pp
-
B. A. Trofimov, N. A. Nedolya, in Comprehensive Heterocyclic Chemistry III, Vol. 3 (Eds.:, G. Jones, C. A. Ramsden,), Elsevier, Oxford, 2008, pp. 88-161.
-
(2008)
Comprehensive Heterocyclic Chemistry III, Vol. 3
, pp. 88-161
-
-
Trofimov, B.A.1
Nedolya, N.A.2
-
5
-
-
79953229372
-
-
Recent reviews
-
Recent reviews
-
-
-
-
7
-
-
17744417463
-
-
Angew. Chem. Int. Ed. 2003, 42, 3582-3603
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3582-3603
-
-
-
8
-
-
33746162485
-
-
See also the following recent reports
-
M. G. Banwell, T. E. Goodwin, S. Ng, J. A. Smith, D. J. Wong, Eur. J. Org. Chem. 2006, 3043-3060. See also the following recent reports
-
(2006)
Eur. J. Org. Chem.
, pp. 3043-3060
-
-
Banwell, M.G.1
Goodwin, T.E.2
Ng, S.3
Smith, J.A.4
Wong, D.J.5
-
9
-
-
3543120754
-
-
N. K. Garg, D. D. Caspi, B. M. Stoltz, J. Am. Chem. Soc. 2004, 126, 9552-9553
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9552-9553
-
-
Garg, N.K.1
Caspi, D.D.2
Stoltz, B.M.3
-
11
-
-
34250629941
-
-
A. Fürstner, K. Radkowski, H. Peters, G. Seidel, C. Wirtz, R. Mynott, C. W. Lehmann, Chem. Eur. J. 2007, 13, 1929-1945
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 1929-1945
-
-
Fürstner, A.1
Radkowski, K.2
Peters, H.3
Seidel, G.4
Wirtz, C.5
Mynott, R.6
Lehmann, C.W.7
-
12
-
-
49049085250
-
-
T. Kawasaki, F. Sakurai, Y. Hayakawa, J. Nat. Prod. 2008, 71, 1265-1267
-
(2008)
J. Nat. Prod.
, vol.71
, pp. 1265-1267
-
-
Kawasaki, T.1
Sakurai, F.2
Hayakawa, Y.3
-
13
-
-
57349119305
-
-
M. Oberhuber, J. Berghold, B. Kräutler, Angew. Chem. 2008, 120, 3100-3104
-
(2008)
Angew. Chem.
, vol.120
, pp. 3100-3104
-
-
Oberhuber, M.1
Berghold, J.2
Kräutler, B.3
-
14
-
-
44949110394
-
-
Angew. Chem. Int. Ed. 2008, 47, 3057-3061
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3057-3061
-
-
-
16
-
-
79953203022
-
-
For selected recent examples, see
-
For selected recent examples, see
-
-
-
-
17
-
-
2142777877
-
-
N. J. Meltola, R. Wahlroos, A. E. Soini, J. Fluoresc. 2004, 14, 635-647
-
(2004)
J. Fluoresc.
, vol.14
, pp. 635-647
-
-
Meltola, N.J.1
Wahlroos, R.2
Soini, A.E.3
-
18
-
-
8344271014
-
-
G. Zotti, S. Zecchin, G. Schiavon, B. Vercelli, A. Berlin, S. Grimoldi, Macromol. Chem. Phys. 2004, 205, 2026-2031
-
(2004)
Macromol. Chem. Phys.
, vol.205
, pp. 2026-2031
-
-
Zotti, G.1
Zecchin, S.2
Schiavon, G.3
Vercelli, B.4
Berlin, A.5
Grimoldi, S.6
-
19
-
-
20744442585
-
-
H. Xu, G. Yu, W. Xu, Y. Xu, G. Cui, D. Zhang, Y. Liu, D. Zhu, Langmuir 2005, 21, 5391-5395
-
(2005)
Langmuir
, vol.21
, pp. 5391-5395
-
-
Xu, H.1
Yu, G.2
Xu, W.3
Xu, Y.4
Cui, G.5
Zhang, D.6
Liu, Y.7
Zhu, D.8
-
20
-
-
27744529665
-
-
R. C. Foitzik, A. Kaynak, J. Beckmann, F. M. Pfeffer, Synth. Met. 2005, 155, 185-190
-
(2005)
Synth. Met.
, vol.155
, pp. 185-190
-
-
Foitzik, R.C.1
Kaynak, A.2
Beckmann, J.3
Pfeffer, F.M.4
-
22
-
-
33747615010
-
-
R. C. Foitzik, A. Kaynak, F. M. Pfeffer, Synth. Met. 2006, 156, 637-642
-
(2006)
Synth. Met.
, vol.156
, pp. 637-642
-
-
Foitzik, R.C.1
Kaynak, A.2
Pfeffer, F.M.3
-
23
-
-
33846575675
-
-
R. C. Foitzik, A. Kaynak, F. M. Pfeffer, J. Beckmann, Synth. Met. 2006, 156, 1333-1340
-
(2006)
Synth. Met.
, vol.156
, pp. 1333-1340
-
-
Foitzik, R.C.1
Kaynak, A.2
Pfeffer, F.M.3
Beckmann, J.4
-
24
-
-
35348907285
-
-
L. Jiao, E. Hao, G. H. Vicente, K. M. Smith, J. Org. Chem. 2007, 72, 8119-8122
-
(2007)
J. Org. Chem.
, vol.72
, pp. 8119-8122
-
-
Jiao, L.1
Hao, E.2
Vicente, G.H.3
Smith, K.M.4
-
25
-
-
34250643162
-
-
R. Chan Yu King, M. Boussoualem, F. Roussel, Polymer 2007, 48, 4047-4054
-
(2007)
Polymer
, vol.48
, pp. 4047-4054
-
-
Chan Yu King, R.1
Boussoualem, M.2
Roussel, F.3
-
26
-
-
38949161883
-
-
G. Zotti, B. Vercelli, A. Berlin, Chem. Mater. 2008, 20, 397-412.
-
(2008)
Chem. Mater.
, vol.20
, pp. 397-412
-
-
Zotti, G.1
Vercelli, B.2
Berlin, A.3
-
27
-
-
79953184113
-
-
For example, see
-
For example, see
-
-
-
-
28
-
-
0016390648
-
-
B. J. Whitlock, H. W. Whitlock, H. Alles, J. Am. Chem. Soc. 1974, 96, 3959-3965
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 3959-3965
-
-
Whitlock, B.J.1
Whitlock, H.W.2
Alles, H.3
-
29
-
-
7044222963
-
-
S. Neya, J. Quan, T. Hoshino, M. Hata, N. Funasaki, Tetrahedron Lett. 2004, 45, 8629-8630
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8629-8630
-
-
Neya, S.1
Quan, J.2
Hoshino, T.3
Hata, M.4
Funasaki, N.5
-
30
-
-
19844369992
-
-
See also the following recent review
-
C. Ryppa, M. O. Senge, S. S. Hatscher, E. Kleinpeter, P. Wacker, U. Schilde, A. Wiehe, Chem. Eur. J. 2005, 11, 3427-3442. See also the following recent review
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 3427-3442
-
-
Ryppa, C.1
Senge, M.O.2
Hatscher, S.S.3
Kleinpeter, E.4
Wacker, P.5
Schilde, U.6
Wiehe, A.7
-
31
-
-
43949131442
-
-
N. Ono, Heterocycles 2008, 75, 243-284.
-
(2008)
Heterocycles
, vol.75
, pp. 243-284
-
-
Ono, N.1
-
32
-
-
79953177154
-
-
For example, see
-
For example, see
-
-
-
-
33
-
-
0033521103
-
-
H. Shiraishi, T. Nishitani, T. Nishihara, S. Sakaguchi, Y. Ishii, Tetrahedron 1999, 55, 13957-13964
-
(1999)
Tetrahedron
, vol.55
, pp. 13957-13964
-
-
Shiraishi, H.1
Nishitani, T.2
Nishihara, T.3
Sakaguchi, S.4
Ishii, Y.5
-
34
-
-
0035796535
-
-
F. J. Fañanás, A. Granados, R. Sanz, J. M. Ignacio, J. Barluenga, Chem. Eur. J. 2001, 7, 2896-2907
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 2896-2907
-
-
Fañanás, F.J.1
Granados, A.2
Sanz, R.3
Ignacio, J.M.4
Barluenga, J.5
-
36
-
-
77954610431
-
-
S. Lamandé-Langle, M. Abarbri, J. Thibonnet, A. Duchene, J.-L. Parrain, Chem. Commun. 2010, 46, 5157-5159.
-
(2010)
Chem. Commun.
, vol.46
, pp. 5157-5159
-
-
Lamandé-Langle, S.1
Abarbri, M.2
Thibonnet, J.3
Duchene, A.4
Parrain, J.-L.5
-
37
-
-
79953190924
-
-
For selected recent reports, see
-
For selected recent reports, see
-
-
-
-
38
-
-
70349683306
-
-
M. P. Sibi, J. Coulomb, L. M. Stanley, Angew. Chem. 2008, 120, 10061-10063
-
(2008)
Angew. Chem.
, vol.120
, pp. 10061-10063
-
-
Sibi, M.P.1
Coulomb, J.2
Stanley, L.M.3
-
39
-
-
57549091031
-
-
Angew. Chem. Int. Ed. 2008, 47, 9913-9915
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 9913-9915
-
-
-
40
-
-
67649407393
-
-
S. Yamazaki, S. Kashima, T. Kuriyama, Y. Iwata, Y. Morimoto, K. Kakiuchi, Tetrahedron: Asymmetry 2009, 20, 1224-1234
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1224-1234
-
-
Yamazaki, S.1
Kashima, S.2
Kuriyama, T.3
Iwata, Y.4
Morimoto, Y.5
Kakiuchi, K.6
-
41
-
-
77749280072
-
-
Y. Huang, E. Tokunaga, S. Suzuki, M. Shiro, N. Shibata, Org. Lett. 2010, 12, 1136-1138
-
(2010)
Org. Lett.
, vol.12
, pp. 1136-1138
-
-
Huang, Y.1
Tokunaga, E.2
Suzuki, S.3
Shiro, M.4
Shibata, N.5
-
42
-
-
75749087217
-
-
W. Wang, X. Liu, W. Cao, J. Wang, L. Lin, X. Feng, Chem. Eur. J. 2010, 16, 1664-1669.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 1664-1669
-
-
Wang, W.1
Liu, X.2
Cao, W.3
Wang, J.4
Lin, L.5
Feng, X.6
-
43
-
-
79953198082
-
-
For example, see
-
For example, see
-
-
-
-
44
-
-
33645943696
-
-
J. Liu, E. Muth, U. Flörke, G. Henkel, K. Merz, J. Sauvageau, E. Schwake, G. Dyker, Adv. Synth. Catal. 2006, 348, 456-462
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 456-462
-
-
Liu, J.1
Muth, E.2
Flörke, U.3
Henkel, G.4
Merz, K.5
Sauvageau, J.6
Schwake, E.7
Dyker, G.8
-
46
-
-
33846534769
-
-
For example, see
-
For example, see:, J. S. Yadav, B. V. S. Reddy, K. V. Rao, P. P. Rao, K. S. Raj, A. R. Prasad, A. Prabhakar, B. Jagadeesh, Synlett 2006, 3447-3450.
-
(2006)
Synlett
, pp. 3447-3450
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Rao, K.V.3
Rao, P.P.4
Raj, K.S.5
Prasad, A.R.6
Prabhakar, A.7
Jagadeesh, B.8
-
47
-
-
61449178929
-
-
For example, see
-
For example, see:, G. Blay, I. Fernández, A. Monleõn, J. R. Pedro, C. Vila, Org. Lett. 2009, 11, 441-444.
-
(2009)
Org. Lett.
, vol.11
, pp. 441-444
-
-
Blay, G.1
Fernández, I.2
Monleõn, A.3
Pedro, J.R.4
Vila, C.5
-
48
-
-
35048845079
-
-
For example, see
-
For example, see:, G. Li, G. B. Rowland, E. B. Rowland, J. C. Antilla, Org. Lett. 2007, 9, 4065-4068.
-
(2007)
Org. Lett.
, vol.9
, pp. 4065-4068
-
-
Li, G.1
Rowland, G.B.2
Rowland, E.B.3
Antilla, J.C.4
-
49
-
-
79953209513
-
-
For example, see
-
For example, see
-
-
-
-
51
-
-
58149344918
-
-
Y.-H. Liu, Q.-S. Liu, Z.-H. Zhang, Tetrahedron Lett. 2009, 50, 916-921.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 916-921
-
-
Liu, Y.-H.1
Liu, Q.-S.2
Zhang, Z.-H.3
-
52
-
-
0141922936
-
-
For example, see
-
For example, see:, J. S. Yadav, B. V. S. Reddy, G. Satheesh, Tetrahedron Lett. 2003, 44, 8331-8334.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 8331-8334
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Satheesh, G.3
-
53
-
-
79953168238
-
-
Reviews including significant references on the subject have been reported
-
Reviews including significant references on the subject have been reported
-
-
-
-
55
-
-
0042869554
-
-
C. Rücker, Chem. Rev. 1995, 95, 1009-1064
-
(1995)
Chem. Rev.
, vol.95
, pp. 1009-1064
-
-
Rücker, C.1
-
57
-
-
27144453995
-
-
L. I. Belen′kill, T. G. Kim, I. A. Suslov, N. D. Chuvylkin, Russ. Chem. Bull. 2005, 54, 853-863
-
(2005)
Russ. Chem. Bull.
, vol.54
, pp. 853-863
-
-
Belenkill, L.I.1
Kim, T.G.2
Suslov, I.A.3
Chuvylkin, N.D.4
-
58
-
-
33751091528
-
-
B. Jolicoeur, E. E. Chapman, A. Thompson, W. D. Lubell, Tetrahedron 2006, 62, 11531-11563
-
(2006)
Tetrahedron
, vol.62
, pp. 11531-11563
-
-
Jolicoeur, B.1
Chapman, E.E.2
Thompson, A.3
Lubell, W.D.4
-
60
-
-
79953224626
-
-
6 th ed. (Eds.: M. B. Smith, J. March), Wiley, New York, pp
-
March's Advanced Organic Chemistry: Reactions Mechanism and Structure, 6 th ed., (Eds.: M. B. Smith, J. March,), Wiley, New York, 2007, pp. 665-670.
-
(2007)
March's Advanced Organic Chemistry: Reactions Mechanism and Structure
, pp. 665-670
-
-
-
61
-
-
79953221999
-
-
5 th ed. (Eds.: J. A. Joule, K. Mills), Wiley, New York, p
-
Heterocyclic Chemistry, 5 th ed., (Eds.: J. A. Joule, K. Mills,), Wiley, New York, 2010, p. 291.
-
(2010)
Heterocyclic Chemistry
, pp. 291
-
-
-
65
-
-
79953228319
-
-
2H and CN), the first stage to introduce the EWG to the parent pyrrole may be omitted
-
2H and CN), the first stage to introduce the EWG to the parent pyrrole may be omitted.
-
-
-
-
67
-
-
0004583006
-
-
J. K. Groves, H. J. Anderson, H. Nagy, Can. J. Chem. 1971, 49, 2427-2432.
-
(1971)
Can. J. Chem.
, vol.49
, pp. 2427-2432
-
-
Groves, J.K.1
Anderson, H.J.2
Nagy, H.3
-
68
-
-
79953230665
-
-
Removal of the EWG is well documented in reference [14a]
-
Removal of the EWG is well documented in reference [14a].
-
-
-
-
69
-
-
0038192981
-
-
For example, see
-
For example, see:, P. E. Sonnet, J. Org. Chem. 1972, 37, 925-929.
-
(1972)
J. Org. Chem.
, vol.37
, pp. 925-929
-
-
Sonnet, P.E.1
-
70
-
-
0013501115
-
-
See also the following report for the preparation of N-MgBr-pyrrole
-
C. E. Loader, H. J. Anderson, Tetrahedron 1969, 25, 3879-3885. See also the following report for the preparation of N-MgBr-pyrrole
-
(1969)
Tetrahedron
, vol.25
, pp. 3879-3885
-
-
Loader, C.E.1
Anderson, H.J.2
-
72
-
-
1942460740
-
-
R. X. Xu, H. J. Anderson, N. J. Gogan, C. E. Loader, R. McDonald, Tetrahedron Lett. 1981, 22, 4899-4900
-
(1981)
Tetrahedron Lett.
, vol.22
, pp. 4899-4900
-
-
Xu, R.X.1
Anderson, H.J.2
Gogan, N.J.3
Loader, C.E.4
McDonald, R.5
-
73
-
-
0001383512
-
-
J. Rokach, P. Hamel, M. Kakushima, Tetrahedron Lett. 1981, 22, 4901-4904.
-
(1981)
Tetrahedron Lett.
, vol.22
, pp. 4901-4904
-
-
Rokach, J.1
Hamel, P.2
Kakushima, M.3
-
74
-
-
0000624987
-
-
See also
-
H. J. Anderson, C. E. Loader, R. X. Xu, N. Lê, N. J. Gogan, R. McDonald, L. G. Edwards, Can. J. Chem. 1985, 63, 896-902. See also
-
(1985)
Can. J. Chem.
, vol.63
, pp. 896-902
-
-
Anderson, H.J.1
Loader, C.E.2
Xu, R.X.3
Lê, N.4
Gogan, N.J.5
McDonald, R.6
Edwards, L.G.7
-
76
-
-
73549086640
-
-
(Ed.: Z. Wang), Wiley, New York, pp
-
Comprehensive Organic Name Reactions and Reagents, Vol. 3 (Ed.:, Z. Wang,), Wiley, New York, 2009, pp. 3018-3025.
-
(2009)
Comprehensive Organic Name Reactions and Reagents, Vol. 3
, pp. 3018-3025
-
-
-
77
-
-
0001407873
-
-
M. Kakushima, P. Hamel, R. Frenette, J. Rokach, J. Org. Chem. 1983, 48, 3214-3219.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 3214-3219
-
-
Kakushima, M.1
Hamel, P.2
Frenette, R.3
Rokach, J.4
-
78
-
-
79953213850
-
-
For selected other examples of α-selective acylation of 12, see
-
For selected other examples of α-selective acylation of 12, see
-
-
-
-
80
-
-
9644266911
-
-
C. Song, D. W. Knight, M. A. Whatton, Tetrahedron Lett. 2004, 45, 9573-9576.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 9573-9576
-
-
Song, C.1
Knight, D.W.2
Whatton, M.A.3
-
81
-
-
79953199224
-
-
For example, see
-
For example, see
-
-
-
-
82
-
-
0043172453
-
-
B. P. J. de Lacy Costello, N. M. Ratcliffe, P. S. Sivanand, Synth. Met. 2003, 139, 43-55
-
(2003)
Synth. Met.
, vol.139
, pp. 43-55
-
-
De Lacy Costello, B.P.J.1
Ratcliffe, N.M.2
Sivanand, P.S.3
-
83
-
-
28544452723
-
-
N. J. L. Guernion, A. Blencowe, W. Hayes, P. Lozano-Sanchez, S. Skaarup, React. Funct. Polym. 2006, 66, 201-218.
-
(2006)
React. Funct. Polym.
, vol.66
, pp. 201-218
-
-
Guernion, N.J.L.1
Blencowe, A.2
Hayes, W.3
Lozano-Sanchez, P.4
Skaarup, S.5
-
84
-
-
0023416306
-
-
E. E. Havinga, L. W. van Horssen, W. ten Hoeve, H. Wynberg, E. W. Meijer, Polym. Bull. 1987, 18, 277-281.
-
(1987)
Polym. Bull.
, vol.18
, pp. 277-281
-
-
Havinga, E.E.1
Van Horssen, L.W.2
Ten Hoeve, W.3
Wynberg, H.4
Meijer, E.W.5
-
85
-
-
0001156279
-
-
J. Rühe, T. Ezquerra, G. Wegner, Makromol. Chem. Rapid Commun. 1989, 10, 103-108
-
(1989)
Makromol. Chem. Rapid Commun.
, vol.10
, pp. 103-108
-
-
Rühe, J.1
Ezquerra, T.2
Wegner, G.3
-
86
-
-
0024301382
-
-
CC 181
-
J. Rühe, T. A. Ezquerra, G. Wegner, Synth. Met. 1989, 28, C 177 -C 181.
-
(1989)
Synth. Met.
, vol.28
, pp. 177
-
-
Rühe, J.1
Ezquerra, T.A.2
Wegner, G.3
-
87
-
-
79953229738
-
-
For selected examples, see
-
For selected examples, see
-
-
-
-
89
-
-
0037197611
-
-
N. Guernion, B. P. J. de Lacy Costello, N. M. Ratcliffe, Synth. Met. 2002, 128, 139-147
-
(2002)
Synth. Met.
, vol.128
, pp. 139-147
-
-
Guernion, N.1
De Lacy Costello, B.P.J.2
Ratcliffe, N.M.3
-
90
-
-
24644470159
-
-
J. Travas-Sejdic, H. Peng, P. A. Kilmartin, M. B. Cannell, G. A. Bowmaker, R. P. Cooney, C. Soeller, Synth. Met. 2005, 152, 37-40.
-
(2005)
Synth. Met.
, vol.152
, pp. 37-40
-
-
Travas-Sejdic, J.1
Peng, H.2
Kilmartin, P.A.3
Cannell, M.B.4
Bowmaker, G.A.5
Cooney, R.P.6
Soeller, C.7
-
91
-
-
79953214236
-
-
For example, see
-
For example, see
-
-
-
-
92
-
-
0033617140
-
-
A. Zelikin, V. R. Shastri, R. Langer, J. Org. Chem. 1999, 64, 3379-3380
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3379-3380
-
-
Zelikin, A.1
Shastri, V.R.2
Langer, R.3
-
93
-
-
25844460698
-
-
J. M. Freitas, L. M. Abrantes, T. Darbre, Helv. Chim. Acta 2005, 88, 2470-2478.
-
(2005)
Helv. Chim. Acta
, vol.88
, pp. 2470-2478
-
-
Freitas, J.M.1
Abrantes, L.M.2
Darbre, T.3
-
94
-
-
38349168986
-
-
For other mechanistic considerations, see reference [27], and references therein
-
J. W. Huffman, V. J. Smith, L. W. Padgett, Tetrahedron 2008, 64, 2104-2112. For other mechanistic considerations, see reference [27], and references therein.
-
(2008)
Tetrahedron
, vol.64
, pp. 2104-2112
-
-
Huffman, J.W.1
Smith, V.J.2
Padgett, L.W.3
-
95
-
-
0000377405
-
-
For selective β-alkylation of N-tBu-pyrrole upon treatment with ethyl diazoacetate in the presence of a copper catalyst, see
-
For selective β-alkylation of N-tBu-pyrrole upon treatment with ethyl diazoacetate in the presence of a copper catalyst, see:, B. E. Maryanoff, J. Org. Chem. 1979, 44, 4410-4419.
-
(1979)
J. Org. Chem.
, vol.44
, pp. 4410-4419
-
-
Maryanoff, B.E.1
-
96
-
-
79953186263
-
-
EAr process and also other transformations, see
-
EAr process and also other transformations, see
-
-
-
-
97
-
-
33644658464
-
-
E. M. Beck, N. P. Grimster, R. Hatley, M. J. Ganut, J. Am. Chem. Soc. 2006, 128, 2528-2529
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2528-2529
-
-
Beck, E.M.1
Grimster, N.P.2
Hatley, R.3
Ganut, M.J.4
-
98
-
-
33845336457
-
-
K. L. Billingsley, K. W. Anderson, S. L. Buchwald, Angew. Chem. 2006, 118, 3564-3568
-
(2006)
Angew. Chem.
, vol.118
, pp. 3564-3568
-
-
Billingsley, K.L.1
Anderson, K.W.2
Buchwald, S.L.3
-
99
-
-
33746256441
-
-
Angew. Chem. Int. Ed. 2006, 45, 3484-3488
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3484-3488
-
-
-
100
-
-
64349115739
-
-
M. D. Morrison, J. J. Hanthorn, D. A. Pratt, Org. Lett. 2009, 11, 1051-1054
-
(2009)
Org. Lett.
, vol.11
, pp. 1051-1054
-
-
Morrison, M.D.1
Hanthorn, J.J.2
Pratt, D.A.3
-
101
-
-
60749134373
-
-
C. Ayats, R. Soley, F. Albericio, M. Úlvarez, Org. Biomol. Chem. 2009, 7, 860-862.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 860-862
-
-
Ayats, C.1
Soley, R.2
Albericio, F.3
Úlvarez, M.4
-
102
-
-
79953204125
-
-
Although the TIPS group is removed from pyrroles in general by treatment with tetrabutylammonium fluoride (TBAF) in THF, the following systems also are available. For NaOMe in MeOH
-
Although the TIPS group is removed from pyrroles in general by treatment with tetrabutylammonium fluoride (TBAF) in THF, the following systems also are available. For NaOMe in MeOH
-
-
-
-
105
-
-
0037193149
-
-
P. N. Collier, I. Patel, R. J. K. Taylor, Tetrahedron Lett. 2002, 43, 3401-3405.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3401-3405
-
-
Collier, P.N.1
Patel, I.2
Taylor, R.J.K.3
-
106
-
-
0000396935
-
-
Synthesis of 17 and its β-selective functionalization were first introduced by Muchowski and co-workers
-
Synthesis of 17 and its β-selective functionalization were first introduced by Muchowski and co-workers:, J. M. Muchowski, D. R. Solas, Tetrahedron Lett. 1983, 24, 3455-3456.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 3455-3456
-
-
Muchowski, J.M.1
Solas, D.R.2
-
107
-
-
0035995694
-
-
D. J. Armitt, M. G. Banwell, C. Freeman, C. R. Parish, J. Chem. Soc. Perkin Trans. 1 2002, 1743-1745
-
(2002)
J. Chem. Soc. Perkin Trans. 1
, pp. 1743-1745
-
-
Armitt, D.J.1
Banwell, M.G.2
Freeman, C.3
Parish, C.R.4
-
108
-
-
0038509986
-
-
B. Kempf, N. Hampel, A. R. Ofial, H. Mayr, Chem. Eur. J. 2003, 9, 2209-2218
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 2209-2218
-
-
Kempf, B.1
Hampel, N.2
Ofial, A.R.3
Mayr, H.4
-
109
-
-
46749114402
-
-
C. Berini, F. Minassian, N. Pelloux-Léon, J.-N. Denis, Y. Vallée, C. Philouze, Org. Biomol. Chem. 2008, 6, 2574-2586.
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 2574-2586
-
-
Berini, C.1
Minassian, F.2
Pelloux-Léon, N.3
Denis, J.-N.4
Vallée, Y.5
Philouze, C.6
-
111
-
-
33751554339
-
-
B. L. Bray, P. H. Mathies, R. Naef, D. R. Solas, T. T. Tidwell, D. R. Artis, J. M. Muchowski, J. Org. Chem. 1990, 55, 6317-6328.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 6317-6328
-
-
Bray, B.L.1
Mathies, P.H.2
Naef, R.3
Solas, D.R.4
Tidwell, T.T.5
Artis, D.R.6
Muchowski, J.M.7
-
112
-
-
79953183806
-
-
After the publication by Muchowski and co-workers, two research groups reported the same reaction sequences
-
After the publication by Muchowski and co-workers, two research groups reported the same reaction sequences
-
-
-
-
114
-
-
84985698675
-
-
See also a recent example
-
K.-P. Stefan, W. Schuhmann, H. Parlar, F. Korte, Chem. Ber. 1989, 122, 169-174. See also a recent example
-
(1989)
Chem. Ber.
, vol.122
, pp. 169-174
-
-
Stefan, K.-P.1
Schuhmann, W.2
Parlar, H.3
Korte, F.4
-
116
-
-
33746175848
-
-
N. A. Bumagin, A. F. Sokolova, I. P. Beletskaya, G. Wolz, Russ. J. Org. Chem. 1993, 29, 136-137
-
(1993)
Russ. J. Org. Chem.
, vol.29
, pp. 136-137
-
-
Bumagin, N.A.1
Sokolova, A.F.2
Beletskaya, I.P.3
Wolz, G.4
-
117
-
-
0000749774
-
-
N. A. Bumagin, A. F. Nikitina, I. P. Beletskaya, Russ. J. Org. Chem. 1994, 30, 1619-1629.
-
(1994)
Russ. J. Org. Chem.
, vol.30
, pp. 1619-1629
-
-
Bumagin, N.A.1
Nikitina, A.F.2
Beletskaya, I.P.3
-
118
-
-
0037041497
-
-
Y. Hari, S. Obika, M. Sakaki, K. Morio, Y. Yamagata, T. Imanishi, Tetrahedron 2002, 58, 3051-3063.
-
(2002)
Tetrahedron
, vol.58
, pp. 3051-3063
-
-
Hari, Y.1
Obika, S.2
Sakaki, M.3
Morio, K.4
Yamagata, Y.5
Imanishi, T.6
-
119
-
-
0036148678
-
-
F. J. Lopez, M.-F. Jett, J. M. Muchowski, D. Nitzan, C. O'Yang, Heterocycles 2002, 56, 91-95.
-
(2002)
Heterocycles
, vol.56
, pp. 91-95
-
-
Lopez, F.J.1
Jett, M.-F.2
Muchowski, J.M.3
Nitzan, D.4
O'Yang, C.5
-
121
-
-
0346555499
-
-
A. J. Castro, W. G. Duncan, A. K. Leong, J. Am. Chem. Soc. 1969, 91, 4304.
-
(1969)
J. Am. Chem. Soc.
, vol.91
, pp. 4304
-
-
Castro, A.J.1
Duncan, W.G.2
Leong, A.K.3
-
122
-
-
0037100115
-
-
J. S. Yadav, B. V. S. Reddy, P. M. Reddy, C. Srinivas, Tetrahedron Lett. 2002, 43, 5185-5187.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5185-5187
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Reddy, P.M.3
Srinivas, C.4
-
123
-
-
0001464372
-
-
M. R. DuBois, L. D. Vasquez, L. Peslherbe, B. C. Noll, Organometallics 1999, 18, 2230-2240.
-
(1999)
Organometallics
, vol.18
, pp. 2230-2240
-
-
Dubois, M.R.1
Vasquez, L.D.2
Peslherbe, L.3
Noll, B.C.4
-
124
-
-
0001206570
-
-
W. H. Myers, J. I. Koontz, W. D. Harman, J. Am. Chem. Soc. 1992, 114, 5684-5692
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 5684-5692
-
-
Myers, W.H.1
Koontz, J.I.2
Harman, W.D.3
-
125
-
-
33751385147
-
-
L. M. Hodges, J. Gonzalez, J. I. Koontz, W. H. Myers, W. D. Harman, J. Org. Chem. 1993, 58, 4788-4790
-
(1993)
J. Org. Chem.
, vol.58
, pp. 4788-4790
-
-
Hodges, L.M.1
Gonzalez, J.2
Koontz, J.I.3
Myers, W.H.4
Harman, W.D.5
-
126
-
-
0001175111
-
-
L. M. Hodges, M. W. Moody, W. D. Harman, J. Am. Chem. Soc. 1994, 116, 7931-7932
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 7931-7932
-
-
Hodges, L.M.1
Moody, M.W.2
Harman, W.D.3
-
127
-
-
0001046913
-
-
L. M. Hodges, J. Gonzalez, J. I. Koontz, W. H. Myers, W. D. Harman, J. Org. Chem. 1995, 60, 2125-2146
-
(1995)
J. Org. Chem.
, vol.60
, pp. 2125-2146
-
-
Hodges, L.M.1
Gonzalez, J.2
Koontz, J.I.3
Myers, W.H.4
Harman, W.D.5
-
128
-
-
0029780705
-
-
For reviews, see
-
L. M. Hodges, M. L. Spera, M. W. Moody, W. D. Harman, J. Am. Chem. Soc. 1996, 118, 7117-7127. For reviews, see
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7117-7127
-
-
Hodges, L.M.1
Spera, M.L.2
Moody, M.W.3
Harman, W.D.4
-
130
-
-
33747594619
-
-
in (Ed.: C. J. Moody), JAI Press, Connecticut, pp
-
L. M. Hodges, W. D. Harman, in Advances in Nitrogen Heterocycles, Vol. 3 (Ed.:, C. J. Moody,), JAI Press, Connecticut, 1998, pp. 1-44
-
(1998)
Advances in Nitrogen Heterocycles, Vol. 3
, pp. 1-44
-
-
Hodges, L.M.1
Harman, W.D.2
-
131
-
-
79953177307
-
-
B. C. Brooks, T. B. Gunnoe, W. D. Harman, Coord. Chem. Rev. 2000, 206-207, 2-61.
-
(2000)
Coord. Chem. Rev.
, vol.206-207
, pp. 2-61
-
-
Brooks, B.C.1
Gunnoe, T.B.2
Harman, W.D.3
-
132
-
-
0000466098
-
-
W. H. Myers, N. Sabat, W. D. Harman, J. Am. Chem. Soc. 1991, 113, 6682-6683.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6682-6683
-
-
Myers, W.H.1
Sabat, N.2
Harman, W.D.3
-
133
-
-
0037999876
-
-
M. T. Valahovic, W. H. Myers, W. D. Harman, Organometallics 2002, 21, 4581-4589.
-
(2002)
Organometallics
, vol.21
, pp. 4581-4589
-
-
Valahovic, M.T.1
Myers, W.H.2
Harman, W.D.3
-
134
-
-
66149110343
-
-
T. Tsuchimoto, T. Wagatsuma, K. Aoki, J. Shimotori, Org. Lett. 2009, 11, 2129-2132.
-
(2009)
Org. Lett.
, vol.11
, pp. 2129-2132
-
-
Tsuchimoto, T.1
Wagatsuma, T.2
Aoki, K.3
Shimotori, J.4
-
135
-
-
77955434940
-
-
T. Tsuchimoto, M. Igarashi, K. Aoki, Chem. Eur. J. 2010, 16, 8975-8979.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 8975-8979
-
-
Tsuchimoto, T.1
Igarashi, M.2
Aoki, K.3
-
136
-
-
0142074710
-
-
T. Tsuchimoto, K. Hatanaka, E. Shirakawa, Y. Kawakami, Chem. Commun. 2003, 2454-2455.
-
(2003)
Chem. Commun.
, pp. 2454-2455
-
-
Tsuchimoto, T.1
Hatanaka, K.2
Shirakawa, E.3
Kawakami, Y.4
-
137
-
-
79953173765
-
-
3 (10 mol %), a 85:15 mixture of the corresponding β,β′- and α,β′-adducts is produced. No α,α′-isomer is thus formed. Use of pyrroles with bulkier substituents on the nitrogen atom leads to higher selectivity of 41. For further details, see reference [54]
-
3 (10 mol %), a 85:15 mixture of the corresponding β,β′- and α,β′-adducts is produced. No α,α′-isomer is thus formed. Use of pyrroles with bulkier substituents on the nitrogen atom leads to higher selectivity of 41. For further details, see reference [54].
-
-
-
-
138
-
-
66149135249
-
-
T. Tsuchimoto, T. Ainoya, K. Aoki, T. Wagatsuma, E. Shirakawa, Eur. J. Org. Chem. 2009, 2437-2440.
-
(2009)
Eur. J. Org. Chem.
, pp. 2437-2440
-
-
Tsuchimoto, T.1
Ainoya, T.2
Aoki, K.3
Wagatsuma, T.4
Shirakawa, E.5
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