-
1
-
-
84861499417
-
-
J. L. Hou, X. F. Liu, J. Shen, G. L. Zhao, P. G. Wang, Expert Opin. Drug Discovery 2012, 7, 489
-
(2012)
Expert Opin. Drug Discovery
, vol.7
, pp. 489
-
-
Hou, J.L.1
Liu, X.F.2
Shen, J.3
Zhao, G.L.4
Wang, P.G.5
-
2
-
-
79960964022
-
-
M. Juricek, P. H. J. Kouwer, A. E. Rowan, Chem. Commun. 2011, 47, 8740
-
(2011)
Chem. Commun.
, vol.47
, pp. 8740
-
-
Juricek, M.1
Kouwer, P.H.J.2
Rowan, A.E.3
-
3
-
-
80053528741
-
-
S. G. Agalave, S. R. Maujan, V. S. Pore, Chem-Asian J 2011, 6, 2696
-
(2011)
Chem-Asian J
, vol.6
, pp. 2696
-
-
Agalave, S.G.1
Maujan, S.R.2
Pore, V.S.3
-
6
-
-
0004101860
-
-
(Ed.: A. Padwa), Wiley, New York
-
R. Huisgen in 1, 3-Dipolar Cycloaddition Chemistry (Ed.: A. Padwa), Wiley, New York, 1984, pp. 1-176
-
(1984)
1, 3-Dipolar Cycloaddition Chemistry
, pp. 1-176
-
-
Huisgen, R.1
-
7
-
-
0013064237
-
-
V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708
-
(2002)
Angew. Chem.
, vol.114
, pp. 2708
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
9
-
-
0037012920
-
-
C. W. Tornøe, C. Christensen, M. Meldal, J. Org. Chem. 2002, 67, 3057
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3057
-
-
Tornøe, C.W.1
Christensen, C.2
Meldal, M.3
-
10
-
-
28044465418
-
-
L. Zhang, X. Chen, P. Xue, H. H. Y. Sun, I. D. Williams, K. B. Sharpless, V. V. Fokin, G. Jia, J. Am. Chem. Soc. 2005, 127, 15998
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15998
-
-
Zhang, L.1
Chen, X.2
Xue, P.3
Sun, H.H.Y.4
Williams, I.D.5
Sharpless, K.B.6
Fokin, V.V.7
Jia, G.8
-
13
-
-
84875750598
-
-
refrence therein.
-
S. Chuprakov, S. W. Kwok, V. V. Fokin, J. Am. Chem. Soc. 2013, 135, 4652 and refrence therein.
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 4652
-
-
Chuprakov, S.1
Kwok, S.W.2
Fokin, V.V.3
-
14
-
-
84859375216
-
-
L. Zhang, Z. B. Li, X. J. Wang, N. Yee, C. H. Senanayake, Synlett 2012, 1052
-
(2012)
Synlett
, pp. 1052
-
-
Zhang, L.1
Li, Z.B.2
Wang, X.J.3
Yee, N.4
Senanayake, C.H.5
-
15
-
-
79952834243
-
-
C. A. Baxter, E. Cleator, K. M. J. Brands, J. S. Edwards, R. A. Reamer, F. J. Sheen, G. W. Stewart, N. A. Strotman, D. J. Wallace, Org. Process Res. Dev. 2011, 15, 367
-
(2011)
Org. Process Res. Dev.
, vol.15
, pp. 367
-
-
Baxter, C.A.1
Cleator, E.2
Brands, K.M.J.3
Edwards, J.S.4
Reamer, R.A.5
Sheen, F.J.6
Stewart, G.W.7
Strotman, N.A.8
Wallace, D.J.9
-
16
-
-
77954731181
-
-
C. D. Cox, M. J. Breslin, D. B. Whitman, J. D. Schreier, G. B. McGaughey, M. J. Bogusky, A. J. Roecker, S. P. Mercer, R. A. Bednar, W. Lemaire, J. G. Bruno, D. R. Reiss, C. Meacham Harrell, K. L. Murphy, S. L. Garson, S. M. Doran, T. Prueksaritanont, W. B. Anderson, C. Tang, S. Roller, T. D. Cabalu, D. Cui, G. D. Hartman, S. D. Young, K. S. Koblan, C. J. Winrow, J. J. Renger, P. J. Coleman, J. Med. Chem. 2010, 53, 5320
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5320
-
-
Cox, C.D.1
Breslin, M.J.2
Whitman, D.B.3
Schreier, J.D.4
McGaughey, G.B.5
Bogusky, M.J.6
Roecker, A.J.7
Mercer, S.P.8
Bednar, R.A.9
Lemaire, W.10
Bruno, J.G.11
Reiss, D.R.12
Meacham Harrell, C.13
Murphy, K.L.14
Garson, S.L.15
Doran, S.M.16
Prueksaritanont, T.17
Anderson, W.B.18
Tang, C.19
Roller, S.20
Cabalu, T.D.21
Cui, D.22
Hartman, G.D.23
Young, S.D.24
Koblan, K.S.25
Winrow, C.J.26
Renger, J.J.27
Coleman, P.J.28
more..
-
17
-
-
77957594054
-
-
T. Watanabe, Y. Umezawa, Y. Takahashi, Y. Akamatsu, Bioorg. Med. Chem. Lett. 2010, 20, 5807
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 5807
-
-
Watanabe, T.1
Umezawa, Y.2
Takahashi, Y.3
Akamatsu, Y.4
-
18
-
-
84892573015
-
-
(Portola Pharmaceuticals, Inc., San Francisco, CA), WO2009136995
-
Z. J. Jia, C. Venkataramani, W. Huang, M. Mehrotra, Y. Song, Q. Xu, S. M. Bauer, A. Pandey, (Portola Pharmaceuticals, Inc., San Francisco, CA), WO2009136995, 2009.
-
(2009)
-
-
Jia, Z.J.1
Venkataramani, C.2
Huang, W.3
Mehrotra, M.4
Song, Y.5
Xu, Q.6
Bauer, S.M.7
Pandey, A.8
-
19
-
-
79954618319
-
-
2-aryl-1,2, 3-triazoles, see.
-
2-aryl-1,2, 3-triazoles, see:, W. Yan, Q. Wang, Q. Lin, M. Li, J. L. Petersen, X.-D. Shi, Chem. Eur. J. 2011, 17, 5011.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 5011
-
-
Yan, W.1
Wang, Q.2
Lin, Q.3
Li, M.4
Petersen, J.L.5
Shi, X.-D.6
-
20
-
-
61349086057
-
-
Y. Liu, W. Yan, Y. Chen, J. L. Petersen, X.-D. Shi, Org. Lett. 2008, 10, 5389
-
(2008)
Org. Lett.
, vol.10
, pp. 5389
-
-
Liu, Y.1
Yan, W.2
Chen, Y.3
Petersen, J.L.4
Shi, X.-D.5
-
21
-
-
70350678977
-
-
X.-J. Wang, L. Zhang, H. Lee, N. Haddad, D. Krishnamurthy, C. H. Senanayake, Org. Lett. 2009, 11, 5026
-
(2009)
Org. Lett.
, vol.11
, pp. 5026
-
-
Wang, X.-J.1
Zhang, L.2
Lee, H.3
Haddad, N.4
Krishnamurthy, D.5
Senanayake, C.H.6
-
22
-
-
84867085662
-
-
S. Ueda, M. Su, S. L. Buchwald, Angew. Chem. 2011, 123, 9106
-
(2011)
Angew. Chem.
, vol.123
, pp. 9106
-
-
Ueda, S.1
Su, M.2
Buchwald, S.L.3
-
24
-
-
36049037299
-
-
M. Taillefer, N. Xia, A. Ouali, Angew. Chem. 2007, 119, 952
-
(2007)
Angew. Chem.
, vol.119
, pp. 952
-
-
Taillefer, M.1
Xia, N.2
Ouali, A.3
-
27
-
-
0038263919
-
-
K. S. Balachandran, I. Hiryakkanavar, M. V. George, Tetrahedron 1975, 31, 1171.
-
(1975)
Tetrahedron
, vol.31
, pp. 1171
-
-
Balachandran, K.S.1
Hiryakkanavar, I.2
George, M.V.3
-
28
-
-
47249148754
-
-
Y. Chen, Y. Liu, J. L. Petersen, X.-D. Shi, Chem. Commun. 2008, 3254
-
(2008)
Chem. Commun.
, pp. 3254
-
-
Chen, Y.1
Liu, Y.2
Petersen, J.L.3
Shi, X.-D.4
-
29
-
-
72449173361
-
-
X.-J. Wang, K. Sidhu, L. Zhang, S. Campbell, N. Haddad, D. C. Reeves, D. Krishnamurthy, C. H. Senanayake, Org. Lett. 2009, 11, 5490
-
(2009)
Org. Lett.
, vol.11
, pp. 5490
-
-
Wang, X.-J.1
Sidhu, K.2
Zhang, L.3
Campbell, S.4
Haddad, N.5
Reeves, D.C.6
Krishnamurthy, D.7
Senanayake, C.H.8
-
30
-
-
77957847870
-
-
For allylation/propargylation
-
X.-J. Wang, L. Zhang, D. Krishnamurthy, C. H. Senanayake, P. Wipf, Org. Lett. 2010, 12, 4632. For allylation/propargylation
-
(2010)
Org. Lett.
, vol.12
, pp. 4632
-
-
Wang, X.-J.1
Zhang, L.2
Krishnamurthy, D.3
Senanayake, C.H.4
Wipf, P.5
-
31
-
-
0038541849
-
-
S. Kamijo, T. Jin, Z. Huo, Y. Yamamoto, J. Am. Chem. Soc. 2003, 125, 7786
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 7786
-
-
Kamijo, S.1
Jin, T.2
Huo, Z.3
Yamamoto, Y.4
-
32
-
-
1842451887
-
-
S. Kamijo, T. Jin, Z. Huo, Y. Yamamoto, J. Org. Chem. 2004, 69, 2386
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2386
-
-
Kamijo, S.1
Jin, T.2
Huo, Z.3
Yamamoto, Y.4
-
33
-
-
77955128787
-
-
For hydroxymethylation, see
-
W. Yan, Q. Wang, Y. Chen, J. L. Petersen, X.-D. Shi, Org. Lett. 2010, 12, 3308. For hydroxymethylation, see
-
(2010)
Org. Lett.
, vol.12
, pp. 3308
-
-
Yan, W.1
Wang, Q.2
Chen, Y.3
Petersen, J.L.4
Shi, X.-D.5
-
34
-
-
49649125888
-
-
For vinylation/allenylation, see
-
J. Kalisiak, K. B. Sharpless, V. V. Fokin, Org. Lett. 2008, 10, 3171. For vinylation/allenylation, see
-
(2008)
Org. Lett.
, vol.10
, pp. 3171
-
-
Kalisiak, J.1
Sharpless, K.B.2
Fokin, V.V.3
-
35
-
-
84858391880
-
-
W. Yan, X. Ye, K. Weise, J. L. Petersen, X.-D. Shi, Chem. Commun. 2012, 48, 3521
-
(2012)
Chem. Commun.
, vol.48
, pp. 3521
-
-
Yan, W.1
Ye, X.2
Weise, K.3
Petersen, J.L.4
Shi, X.-D.5
-
36
-
-
67649641716
-
-
H. Duan, W. Yan, S. Sengupta, X.-D. Shi, Bioorg. Med. Chem. Lett. 2009, 19, 3899.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3899
-
-
Duan, H.1
Yan, W.2
Sengupta, S.3
Shi, X.-D.4
-
38
-
-
77956494330
-
-
(Ed.: E. J. Thomas), Thieme, Stuttgart, Chapter
-
"Indole and its Derivatives": J. A. Joule in Science of Synthesis (Houben-Weyl Methods of Molecular Transformations), Vol. 10 (Ed.:, E. J. Thomas,), Thieme, Stuttgart, 2000, Chapter 10.13
-
(2000)
"indole and Its Derivatives": J. A. Joule in Science of Synthesis (Houben-Weyl Methods of Molecular Transformations), Vol. 10
-
-
-
47
-
-
24644504824
-
-
S. Agarwal, S. Cämmerer, S. Filali, W. Froöhner, J. Knöll, M. P. Krahl, K. R. Reddy, H.-J. Knölker, Curr. Org. Chem. 2005, 9, 1601
-
(2005)
Curr. Org. Chem.
, vol.9
, pp. 1601
-
-
Agarwal, S.1
Cämmerer, S.2
Filali, S.3
Froöhner, W.4
Knöll, J.5
Krahl, M.P.6
Reddy, K.R.7
Knölker, H.-J.8
-
48
-
-
19944413632
-
-
M. Bandini, A. Melloni, S. Tommasi, A. Umani-Ronchi, Synlett 2005, 1199.
-
(2005)
Synlett
, pp. 1199
-
-
Bandini, M.1
Melloni, A.2
Tommasi, S.3
Umani-Ronchi, A.4
-
51
-
-
78651519029
-
-
For a recent example of iodine mediated indole functionalization, see.
-
For a recent example of iodine mediated indole functionalization, see:, Y.-X. Li, K.-G. Ji, H.-X. Wang, S. Ali and Y.-M. Liang, J. Org. Chem. 2011, 76, 744.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 744
-
-
Li, Y.-X.1
Ji, K.-G.2
Wang, H.-X.3
Liang, S.A.A.Y.-M.4
-
53
-
-
77952398665
-
-
M. Poirier, S. Goudreau, J. Poulin, J. Savoie, P. L. Beaulieu, Org. Lett. 2010, 12, 2334.
-
(2010)
Org. Lett.
, vol.12
, pp. 2334
-
-
Poirier, M.1
Goudreau, S.2
Poulin, J.3
Savoie, J.4
Beaulieu, P.L.5
-
54
-
-
84867761321
-
-
S. E. Denmark, W. E. Kuester, M. T. Burk, Angew. Chem. Int. Ed. 2012, 51, 10938.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 10938
-
-
Denmark, S.E.1
Kuester, W.E.2
Burk, M.T.3
-
56
-
-
33645952383
-
-
J. Wang, H. Li, L. S. Zu, W. Wang, Org. Lett. 2006, 8, 1391.
-
(2006)
Org. Lett.
, vol.8
, pp. 1391
-
-
Wang, J.1
Li, H.2
Zu, L.S.3
Wang, W.4
-
57
-
-
59849116051
-
-
For a review of nonnatural fluorescent amino acids, see:, A. R. Katritzky, T. Narindoshvili, Org. Biomol. Chem. 2009, 7, 627 and references therein.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 627
-
-
Katritzky, A.R.1
Narindoshvili, T.2
-
58
-
-
37049107918
-
-
Compound 10 can be obtained as an insoluble white solid through the reaction of 2 a with N-iodosuccinimide 3 a, see.
-
Compound 10 can be obtained as an insoluble white solid through the reaction of 2 a with N-iodosuccinimide 3 a, see:, M. J. Sasse, R. C. Storr, J. Chem. Soc. Perkin Trans. 1 1978, 909.
-
(1978)
J. Chem. Soc. Perkin Trans. 1
, pp. 909
-
-
Sasse, M.J.1
Storr, R.C.2
|