-
1
-
-
0003593740
-
-
Eds, G. M. Coppola, H. F. Schuster, Wiley, New York
-
a) The Chemistry of Hetrocyclic Compounds (Eds.: G. M. Coppola, H. F. Schuster), Wiley, New York, 1981.
-
(1981)
The Chemistry of Hetrocyclic Compounds
-
-
-
4
-
-
70349937261
-
-
Pharmaceutical Chemistry, Drug Synthesis, 1 (Eds. : H. J. Roth, A. Kleemann), Prentice Hall Europe, London, 1988, p. 407.
-
a) Pharmaceutical Chemistry, Drug Synthesis, Vol. 1 (Eds. : H. J. Roth, A. Kleemann), Prentice Hall Europe, London, 1988, p. 407.
-
-
-
-
5
-
-
0033602131
-
-
b) A. H. Li, S. Moro, N. Forsyth, N. Melman, X. D. Ji, K. A. Jacobsen, J. Med. Chem. 1999, 42, 706.
-
(1999)
J. Med. Chem
, vol.42
, pp. 706
-
-
Li, A.H.1
Moro, S.2
Forsyth, N.3
Melman, N.4
Ji, X.D.5
Jacobsen, K.A.6
-
6
-
-
2342633234
-
-
D. Kletsas, W. Li, Z. Han, V. Papadopoulos, Biochem. Pharmacol. 2004, 67, 1927.
-
(2004)
Biochem. Pharmacol
, vol.67
, pp. 1927
-
-
Kletsas, D.1
Li, W.2
Han, Z.3
Papadopoulos, V.4
-
7
-
-
20344363175
-
-
a) B. A. Sweetman, H. Müller-Bunz, P. J. Guiry, Tetrahedron Lett. 2005, 46, 4643.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 4643
-
-
Sweetman, B.A.1
Müller-Bunz, H.2
Guiry, P.J.3
-
9
-
-
0242500892
-
-
V. N. Kozhevnikov, D. N. Koz- hevnikov, T. V. Nikitina, V. L. Rusinov, O. L. Chupakhin, M. Zabel, B. Konig, J. Org. Chem. 2003, 68, 2882.
-
(2003)
J. Org. Chem
, vol.68
, pp. 2882
-
-
Kozhevnikov, V.N.1
Koz- hevnikov, D.N.2
Nikitina, T.V.3
Rusinov, V.L.4
Chupakhin, O.L.5
Zabel, M.6
Konig, B.7
-
10
-
-
0004169871
-
-
Ed, R. Adams, Wiley, New York
-
a) W. M. Whaley, T. R. Govindachari, W. J. Gensler in Organic Reactions, Vol. 6 (Ed.: R. Adams), Wiley, New York, 1951.
-
(1951)
Organic Reactions
, vol.6
-
-
Whaley, W.M.1
Govindachari, T.R.2
Gensler, W.J.3
-
11
-
-
0003607021
-
-
Eds, A. Katritzky, C. W. Rees, E. F. V. Scriven, Pergamon, Oxford
-
b)G. Jones in Comprehensive Heterocyclic Chemistry II, Vol. 5 (Eds.: A. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon, Oxford, 1996.
-
(1996)
Comprehensive Heterocyclic Chemistry II
, vol.5
-
-
Jones, G.1
-
12
-
-
70349962566
-
-
D. S. Coffey, S. P. Kolis, S. A. May in Progress in Heterocyclic Chemistry, 14 (Eds. : G. W. Gribble, T. L. Gilchrist), Pergamon, Amsterdam, 2002, Chapter 6.1.
-
a) D. S. Coffey, S. P. Kolis, S. A. May in Progress in Heterocyclic Chemistry, Vol. 14 (Eds. : G. W. Gribble, T. L. Gilchrist), Pergamon, Amsterdam, 2002, Chapter 6.1.
-
-
-
-
16
-
-
0042265625
-
-
e) J. Ichikawa, Y. Wada, H. Miyazaki, T. Mori, H. Kuroki, Org. Lett. 2003, 5, 1455.
-
(2003)
Org. Lett
, vol.5
, pp. 1455
-
-
Ichikawa, J.1
Wada, Y.2
Miyazaki, H.3
Mori, T.4
Kuroki, H.5
-
18
-
-
0000264238
-
-
Eds, B. M. Trost, I. Fleming, Pergamon, Oxford
-
b) S. V. Kessar in Comprehensive Organic Synthesis, Vol.4 (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, pp. 483-515.
-
(1991)
Comprehensive Organic Synthesis
, vol.4
, pp. 483-515
-
-
Kessar, S.V.1
-
19
-
-
70349946468
-
-
Ed, S. Patai, Wiley, Chichester, Chapter 18
-
H. Hart in The Chemistry of Triple-Bonded Functional Groups, Supplement C2 (Ed.: S. Patai), Wiley, Chichester, 1994, Chapter 18.
-
(1994)
The Chemistry of Triple-Bonded Functional Groups, Supplement C2
-
-
Hart, H.1
-
20
-
-
70349960888
-
-
H. H. Wenk, M. Winkler, W. Sander, Angew. Chem. 2003, 115, 518; Angew. Chem. Int. Ed. 2003, 42, 502.
-
H. H. Wenk, M. Winkler, W. Sander, Angew. Chem. 2003, 115, 518; Angew. Chem. Int. Ed. 2003, 42, 502.
-
-
-
-
21
-
-
0042211008
-
-
a) N. G. Rondan, L. N. Domelsmith, K. N. Houk, A. T. Bowne, R. H. Levin, Tetrahedron Lett. 1979, 20, 3237
-
(1979)
Tetrahedron Lett
, vol.20
, pp. 3237
-
-
Rondan, N.G.1
Domelsmith, L.N.2
Houk, K.N.3
Bowne, A.T.4
Levin, R.H.5
-
23
-
-
70349953368
-
-
H. Yoshida, E. Shirakawa, Y. Honda, T. Hiyama, Angew. Chem. 2002, 114, 3381; Angew. Chem. Int. Ed. 2002, 41, 3247.
-
H. Yoshida, E. Shirakawa, Y. Honda, T. Hiyama, Angew. Chem. 2002, 114, 3381; Angew. Chem. Int. Ed. 2002, 41, 3247.
-
-
-
-
24
-
-
33748053357
-
-
H. Yoshida, H. Fukushima, J. Ohshita, A. Kunai, J. Am. Chem. Soc. 2006, 128, 11040
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 11040
-
-
Yoshida, H.1
Fukushima, H.2
Ohshita, J.3
Kunai, A.4
-
25
-
-
37549003577
-
-
and references therein
-
e) Z. J. Liu, F. Shi, P. D. G. Martinez, C. Raminelli, R. C. Larock, J. Org. Chem. 2008, 73, 219, and references therein.
-
(2008)
J. Org. Chem
, vol.73
, pp. 219
-
-
Liu, Z.J.1
Shi, F.2
Martinez, P.D.G.3
Raminelli, C.4
Larock, R.C.5
-
26
-
-
38949175721
-
-
f) C. D. Gilmore, K. M. Allan, B. M. Stoltz, J. Am. Chem. Soc. 2008, 130, 1558.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 1558
-
-
Gilmore, C.D.1
Allan, K.M.2
Stoltz, B.M.3
-
27
-
-
33746797933
-
-
a) H. Yoshida, H. Fukushima, J. Ohshita, A. Kunai, Angew. Chem. 2004, 116, 4025;
-
(2004)
Angew. Chem
, vol.116
, pp. 4025
-
-
Yoshida, H.1
Fukushima, H.2
Ohshita, J.3
Kunai, A.4
-
29
-
-
7044231369
-
-
b) H. Yoshida, H. Fukushima, J. Ohshita, A. Kunai, Tetrahedron Lett. 2004, 45, 8659.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 8659
-
-
Yoshida, H.1
Fukushima, H.2
Ohshita, J.3
Kunai, A.4
-
30
-
-
34247272920
-
-
H. Yoshida, H. Fukushima, J. Ohshita, A. Kunai, Tetrahedron 2007, 63, 4793.
-
(2007)
Tetrahedron
, vol.63
, pp. 4793
-
-
Yoshida, H.1
Fukushima, H.2
Ohshita, J.3
Kunai, A.4
-
31
-
-
0000221711
-
-
a)R. Knorr, Chem. Ber. 1965, 98, 4038
-
(1965)
Chem. Ber
, vol.98
, pp. 4038
-
-
Knorr, R.1
-
33
-
-
33745105781
-
-
The resulting aryl anion is available to abstract a proton, thus leading to the formation of monosubstituted arenes. For examples, see: a
-
The resulting aryl anion is available to abstract a proton, thus leading to the formation of monosubstituted arenes. For examples, see: a) M. Jeganmohan, C. H. Cheng, Chem. Commun. 2006, 2454.
-
(2006)
Chem. Commun
, pp. 2454
-
-
Jeganmohan, M.1
Cheng, C.H.2
-
35
-
-
70349927972
-
-
For the reactions of azabutadienes to form azaheterocycles through [4+2] cycloaddition, see: a D. L. Boger, S. M. Weinreb in Hetero Diels-Alder Methodology in Organic Synthesis (Ed.: H. H. Wasserman), Academic Press, New York, 1987, pp. 239 - 299.
-
For the reactions of azabutadienes to form azaheterocycles through [4+2] cycloaddition, see: a) D. L. Boger, S. M. Weinreb in Hetero Diels-Alder Methodology in Organic Synthesis (Ed.: H. H. Wasserman), Academic Press, New York, 1987, pp. 239 - 299.
-
-
-
-
38
-
-
33748057815
-
-
M. D. Fletcher, T. E. Hurst, T. J. Miles, C. J. Moody, Tetrahedron 2006, 62, 5454.
-
(2006)
Tetrahedron
, vol.62
, pp. 5454
-
-
Fletcher, M.D.1
Hurst, T.E.2
Miles, T.J.3
Moody, C.J.4
-
40
-
-
70349962563
-
-
b) D. Pefia, A. Cobas, D. Perez, E. Guitian, Synthesis 2002, 1454.
-
(2002)
Synthesis
, pp. 1454
-
-
Pefia, D.1
Cobas, A.2
Perez, D.3
Guitian, E.4
-
41
-
-
70349975091
-
-
T. Jin, Y. Yamamoto, Angew. Chem. 2007, 119, 3387; Angew. Chem. Int. Ed. 2007, 46, 3323.
-
T. Jin, Y. Yamamoto, Angew. Chem. 2007, 119, 3387; Angew. Chem. Int. Ed. 2007, 46, 3323.
-
-
-
-
42
-
-
70349938891
-
-
By using toluene in MeCN (as the solvent), one can slow the generation of the benzyne and therefore improve the yield of product 5a. For the details, see: Z. J. Lui, R. C. Larock, J. Org. Chem. 2007, 72, 223.
-
By using toluene in MeCN (as the solvent), one can slow the generation of the benzyne and therefore improve the yield of product 5a. For the details, see: Z. J. Lui, R. C. Larock, J. Org. Chem. 2007, 72, 223.
-
-
-
-
43
-
-
70349949925
-
-
Preferential nucleophilic attack at the para position to a chlorine atom also occurred in nucleophilic reactions with p-chloroaryne:
-
Preferential nucleophilic attack at the para position to a chlorine atom also occurred in nucleophilic reactions with p-chloroaryne:
-
-
-
|