-
2
-
-
11144315535
-
-
N. Issaeva, P. Bozko, M. Enge, M. Protopopova, L. G. G. C. Verhoef, M. Masucci, A. Pramanik, G. Selivanova, Nat. Med. 2004, 10, 1321 - 1328.
-
(2004)
Nat. Med.
, vol.10
, pp. 1321-1328
-
-
Issaeva, N.1
Bozko, P.2
Enge, M.3
Protopopova, M.4
Verhoef, L.G.G.C.5
Masucci, M.6
Pramanik, A.7
Selivanova, G.8
-
3
-
-
78349250510
-
-
See, for example
-
See, for example
-
-
-
-
4
-
-
59649084045
-
-
X. Ming, W. Ju, H. Wu, R. R. Tidwell, J. E. Hall, D. R. Thakker, Drug Metab. Dispos. 2009, 37, 424 - 430
-
(2009)
Drug Metab. Dispos.
, vol.37
, pp. 424-430
-
-
Ming, X.1
Ju, W.2
Wu, H.3
Tidwell, R.R.4
Hall, J.E.5
Thakker, D.R.6
-
5
-
-
65349162100
-
-
J. Trop. Med. Hyg. 2009, 528- 535.
-
M. M. Nyunt, C. W. Hendrix, R. P. Bakshi, N. Kumar, T. A. Shapiro, Am. J. Trop. Med. Hyg. 2009, 80, 528- 535.
-
Am.
, pp. 80
-
-
Nyunt, M.M.1
Hendrix, C.W.2
Bakshi, R.P.3
Kumar, N.4
Shapiro, T.A.5
-
6
-
-
67649349011
-
-
(Ed.: I. Ojima), Wiley-Blackwell, Chichester,.
-
E. P. Cormier, M. Das, I. Ojima, Approved Active Pharmaceutical Ingredients Containing Fluorine, in: Fluorine in Medicinal Chemistry and Chemical Biology, (Ed.:, I. Ojima,), Wiley-Blackwell, Chichester, 2009, pp 525 - 603.
-
(2009)
Approved Active Pharmaceutical Ingredients Containing Fluorine, In: Fluorine in Medicinal Chemistry and Chemical Biology
, pp. 525-603
-
-
Cormier, E.P.1
Das, M.2
Ojima, I.3
-
7
-
-
84890169857
-
-
John Wiley & Sons, New York,.
-
J.-P. Bégué, D. Bonnet-Delpon, Bioorganic and Medicinal Chemistry of Fluorine, John Wiley & Sons, New York, 2008, pp 279 - 351.
-
(2008)
Bioorganic and Medicinal Chemistry of Fluorine
, pp. 279-351
-
-
Bégué, J.-P.1
Bonnet-Delpon, D.2
-
9
-
-
76549107901
-
-
Review:
-
Review:, O. Serdyuk, A. Butin, V. Abaev, J. Fluorine Chem. 2010, 131, 296 - 319.
-
(2010)
J. Fluorine Chem.
, vol.131
, pp. 296-319
-
-
Serdyuk, O.1
Butin, A.2
Abaev, V.3
-
10
-
-
10244222420
-
-
A. S. Cantrell, P. Engelhardt, M. Högberg, R. S. Jaskunas, N. G. Johansson, C. L. Jordan, J. Kangasmetsä, M. D. Kinnick, P. Lind, J. M. Morin Jr, M. A. Muesing, R. Noreén, B. Öberg, P. Pranc, C. Sahlberg, R. J. Ternansky, R. T. Vasileff, L. Vrang, S. J. West, H. Zhang, J. Med. Chem. 1996, 39, 4261 - 4274.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4261-4274
-
-
Cantrell, A.S.1
Engelhardt, P.2
Högberg, M.3
Jaskunas, R.S.4
Johansson, N.G.5
Jordan, C.L.6
Kangasmetsä, J.7
Kinnick, M.D.8
Lind, P.9
Morin, Jr.J.M.10
Muesing, M.A.11
Noreén, R.12
Öberg, B.13
Pranc, P.14
Sahlberg, C.15
Ternansky, R.J.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
more..
-
11
-
-
78649489122
-
-
See also:, (Eds.: A. A. Gakh, K. L. Kirk), ACS Symposium Series 1003; American Chemical Society, Washington, DC,.
-
See also:, S. Arimitsu, G. B. Hammond, Synthesis of gem-Difluorinated Heterocycles Using a Difluoropropargyl Molecular Scaffold, in: Fluorinated Heterocycles, (Eds.:, A. A. Gakh, K. L. Kirk,), ACS Symposium Series 1003; American Chemical Society, Washington, DC, 2009, pp 135 - 162.
-
(2009)
Synthesis of Gem-Difluorinated Heterocycles Using A Difluoropropargyl Molecular Scaffold, In: Fluorinated Heterocycles
, pp. 135-162
-
-
Arimitsu, S.1
Hammond, G.B.2
-
12
-
-
0242628417
-
-
E. Dvornikova, M. Bechcicka, K. Kamieńska-Trela, A. Krówczyński, J. Fluorine Chem. 2003, 124, 159 - 168.
-
(2003)
J. Fluorine Chem.
, vol.124
, pp. 159-168
-
-
Dvornikova, E.1
Bechcicka, M.2
Kamieńska-Trela, K.3
Kró wczyński, A.4
-
15
-
-
78349291115
-
-
note
-
Silyloxy-substituted β-fluorofurans are obtained via metallation-silylation of 3-fluorofuran-2(5H)-ones formed as a result of acid-catalyzed cyclization of 2-fluoroalk-2-enoates
-
-
-
-
16
-
-
33750324252
-
-
K. Pomeisl, J. Kvičala, O. Paleta, J. Fluorine Chem. 2006, 127, 1390 - 1397
-
(2006)
J. Fluorine Chem.
, vol.127
, pp. 1390-1397
-
-
Pomeisl, K.1
Kvičala, J.2
Paleta, O.3
-
17
-
-
37349012130
-
-
K. Pomeisl, J. Čejka, J. Kvičala, O. Paleta, Eur. J. Org. Chem. 2007, 5917 - 5925.
-
(2007)
Eur. J. Org. Chem.
, pp. 5917-5925
-
-
Pomeisl, K.1
Čejka, J.2
Kvičala, J.3
Paleta, O.4
-
19
-
-
41649118478
-
-
S. Arimitsu, J. M. Jacobsen, G. B. Hammond, J. Org. Chem. 2008, 73, 2886 - 2889.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 2886-2889
-
-
Arimitsu, S.1
Jacobsen, J.M.2
Hammond, G.B.3
-
21
-
-
54149099168
-
-
P. Li, Z. Chai, G. Zhao, S.-Z. Zhu, Synlett 2008, 2547 - 2551.
-
(2008)
Synlett
, pp. 2547-2551
-
-
Li, P.1
Chai, Z.2
Zhao, G.3
Zhu, S.-Z.4
-
23
-
-
48249087686
-
-
5889, and references cited therein.
-
A. Sniady, A. Durham, M. S. Morreale, A. Marcinek, S. Szafert, T. Lis, K. R. Brzezinska, T. Iwasaki, T. Ohshima, K. Mashima, R. Dembinski, J. Org. Chem. 2008, 73, 5881 - 5889, and references cited therein.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 5881
-
-
Sniady, A.1
Durham, A.2
Morreale, M.S.3
Marcinek, A.4
Szafert, S.5
Lis, T.6
Brzezinska, K.R.7
Iwasaki, T.8
Ohshima, T.9
Mashima, K.10
Dembinski, R.11
-
24
-
-
34147112783
-
-
A. Sniady, A. Durham, M. S. Morreale, K. A. Wheeler, R. Dembinski, Org. Lett. 2007, 9, 1175 - 1178
-
(2007)
Org. Lett.
, vol.9
, pp. 1175-1178
-
-
Sniady, A.1
Durham, A.2
Morreale, M.S.3
Wheeler, K.A.4
Dembinski, R.5
-
25
-
-
58149352253
-
-
For heterocylization reactions leading to pyrroles see:
-
For heterocylization reactions leading to pyrroles see:, P. Wyrbek, A. Sniady, N. Bewick, Y. Li, A. Mikus, K. A. Wheeler, R. Dembinski, Tetrahedron 2009, 65, 1268 - 1275.
-
(2009)
Tetrahedron
, vol.65
, pp. 1268-1275
-
-
Wyrbek, P.1
Sniady, A.2
Bewick, N.3
Li, Y.4
Mikus, A.5
Wheeler, K.A.6
Dembinski, R.7
-
26
-
-
48249148606
-
-
A. Sniady, M. S. Morreale, K. A. Wheeler, R. Dembinski, Eur. J. Org. Chem. 2008, 3449 - 3452
-
(2008)
Eur. J. Org. Chem.
, pp. 3449-3452
-
-
Sniady, A.1
Morreale, M.S.2
Wheeler, K.A.3
Dembinski, R.4
-
27
-
-
18844373078
-
-
A. Sniady, K. A. Wheeler, R. Dembinski, Org. Lett. 2005, 7, 1769 - 1772
-
(2005)
Org. Lett.
, vol.7
, pp. 1769-1772
-
-
Sniady, A.1
Wheeler, K.A.2
Dembinski, R.3
-
28
-
-
0042009107
-
-
M. S. Rao, N. Esho, C. Sergeant, R. Dembinski, J. Org. Chem. 2003, 68, 6788 - 6790.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 6788-6790
-
-
Rao, M.S.1
Esho, N.2
Sergeant, C.3
Dembinski, R.4
-
29
-
-
0000468774
-
-
G. S. Lal, G. P. Pez, R. G. Syvret, Chem. Rev. 1996, 96, 1737 - 1756.
-
(1996)
Chem. Rev.
, vol.96
, pp. 1737-1756
-
-
Lal, G.S.1
Pez, G.P.2
Syvret, R.G.3
-
30
-
-
0000601660
-
-
Studies of product distribution for reactions of NF-type reagents indicate a two-step mechanism via an electron transfer with subsequent fluorine radical transfer:
-
Studies of product distribution for reactions of NF-type reagents indicate a two-step mechanism via an electron transfer with subsequent fluorine radical transfer:, T. Umemoto, S. Fukami, G. Tomizawa, K. Harasawa, K. Kawada, K. Tomita, J. Am. Chem. Soc. 1990, 112, 8563 - 8575.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 8563-8575
-
-
Umemoto, T.1
Fukami, S.2
Tomizawa, G.3
Harasawa, K.4
Kawada, K.5
Tomita, K.6
-
31
-
-
77953417458
-
-
S. C. Wilkinson, R. Salmon, V. Gouverneur, Future Med. Chem. 2009, 1, 847 - 863.
-
(2009)
Future Med. Chem.
, vol.1
, pp. 847-863
-
-
Wilkinson, S.C.1
Salmon, R.2
Gouverneur, V.3
-
32
-
-
68349129686
-
-
M. Schuler, F. Silva, C. Bobbio, A. Tessier, V. Gouverneur, Angew. Chem. 2008, 120, 8045 - 8048
-
(2008)
Angew. Chem.
, vol.120
, pp. 8045-8048
-
-
Schuler, M.1
Silva, F.2
Bobbio, C.3
Tessier, A.4
Gouverneur, V.5
-
33
-
-
54749120024
-
-
Angew. Chem. Int. Ed. 2008, 47, 7927 - 7930.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7927-7930
-
-
-
35
-
-
1642499514
-
-
2 in the presence of propylene oxide in 50% yield:, M. S. F. Lie Ken Jie, M. M. L. Lau, C. N. W. Lam, Lipids 2003, 38, 1293 - 1297.
-
(2003)
Lipids
, vol.38
, pp. 1293-1297
-
-
Jie, M.S.F.L.K.1
Lau, M.M.L.2
Lam, C.N.W.3
-
36
-
-
78349237357
-
-
2 complex for furan synthesis, see
-
2 complex for furan synthesis, see
-
-
-
-
39
-
-
0000706688
-
-
A. S. K. Hashmi, T. L. Ruppert, T. Knöfel, J. W. Bats, J. Org. Chem. 1997, 62, 7295 - 7304.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7295-7304
-
-
Hashmi, A.S.K.1
Ruppert, T.L.2
Knöfel, T.3
Bats, J.W.4
-
40
-
-
0141518524
-
-
M. S. F. Lie Ken Jie, M. M. L. Lau, C. N. W. Lam, M. S. Alam, J. O. Metzger, U. Biermann, Chem. Phys. Lipids 2003, 125, 93 - 101.
-
(2003)
Chem. Phys. Lipids
, vol.125
, pp. 93-101
-
-
Jie, M.S.F.L.K.1
Lau, M.M.L.2
Lam, C.N.W.3
Alam, M.S.4
Metzger, J.O.5
Biermann, U.6
-
45
-
-
77954243448
-
-
70 (in Chinese).
-
Y. Lu, F. Song, X. Jia, Y. Liu, Prog. Chem. 2010, 22, 58 - 70 (in Chinese).
-
(2010)
Prog. Chem.
, vol.22
, pp. 58
-
-
Lu, Y.1
Song, F.2
Jia, X.3
Liu, Y.4
-
46
-
-
78349236520
-
-
note
-
[14]
-
-
-
-
50
-
-
78349239984
-
-
Selected reviews
-
Selected reviews
-
-
-
-
51
-
-
77149130505
-
-
A. Das, S. M. Abu Sohel, R.-S. Liu, Org. Biomol. Chem. 2010, 8, 960 - 979
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 960-979
-
-
Das, A.1
Sohel, S.M.A.2
Liu, R.-S.3
-
52
-
-
51249100498
-
-
A. Arcadi, Chem. Rev. 2008, 108, 3266 - 3325
-
(2008)
Chem. Rev.
, vol.108
, pp. 3266-3325
-
-
Arcadi, A.1
-
54
-
-
51049121927
-
-
Z. G. Li, C. Brouwer, C. He, Chem. Rev. 2008, 108, 3239 - 3265
-
(2008)
Chem. Rev.
, vol.108
, pp. 3239-3265
-
-
Li, Z.G.1
Brouwer, C.2
He, C.3
-
56
-
-
69249116093
-
-
Review:
-
Review:, Y. Yamamoto, I. D. Gridnev, N. T. Patil, T. Jin, Chem. Commun. 2009, 5075 - 5087.
-
(2009)
Chem. Commun.
, pp. 5075-5087
-
-
Yamamoto, Y.1
Gridnev, I.D.2
Patil, N.T.3
Jin, T.4
-
57
-
-
0000396789
-
-
For the gold-catalysed cycloisomerisation of propargyl ketones, see:, - 2385
-
For the gold-catalysed cycloisomerisation of propargyl ketones, see:, A. S. K. Hashmi, L. Schwarz, J.-H. Choi, T. M. Frost, Angew. Chem. 2000, 112, 2382 - 2385
-
(2000)
Angew. Chem.
, vol.112
, pp. 2382
-
-
Hashmi, A.S.K.1
Schwarz, L.2
Choi, J.-H.3
Frost, T.M.4
-
58
-
-
0034600902
-
-
Angew. Chem. Int. Ed. 2000, 39, 2285 - 2288.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 2285-2288
-
-
-
59
-
-
77951153861
-
-
A. S. K. Hashmi, T. D. Ramamurthi, F. Rominger, Adv. Synth. Catal. 2010, 352, 971 - 975
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 971-975
-
-
Hashmi, A.S.K.1
Ramamurthi, T.D.2
Rominger, F.3
-
61
-
-
75249090690
-
-
A. S. K. Hashmi, A. Schuster, F. Rominger, Angew. Chem. 2009, 121, 8396 - 8398
-
(2009)
Angew. Chem.
, vol.121
, pp. 8396-8398
-
-
Hashmi, A.S.K.1
Schuster, A.2
Rominger, F.3
-
62
-
-
70350022778
-
-
Angew. Chem. Int. Ed. 2009, 48, 8247 - 8249
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 8247-8249
-
-
-
63
-
-
70350004081
-
-
D. Weber, M. A. Tarselli, M. R. Gagné, Angew. Chem. 2009, 121, 5843 - 5846
-
(2009)
Angew. Chem.
, vol.121
, pp. 5843-5846
-
-
Weber, D.1
Tarselli, M.A.2
Gagné, M.R.3
-
64
-
-
70349904871
-
-
Angew. Chem. Int. Ed. 2009, 48, 5733 - 5736
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 5733-5736
-
-
-
65
-
-
67749110130
-
-
L.-P. Liu, B. Xu, M. S. Mashuta, G. B. Hammond, J. Am. Chem. Soc. 2008, 130, 17642 - 17643.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 17642-17643
-
-
Liu, L.-P.1
Xu, B.2
Mashuta, M.S.3
Hammond, G.B.4
-
66
-
-
84890711200
-
-
John Wiley & Sons, Hoboken, New Jersey,.
-
W. R. Dolbier Jr, Guide to Fluorine NMR for Organic Chemists, John Wiley & Sons, Hoboken, New Jersey, 2009, pp 89 - 91.
-
(2009)
Guide to Fluorine NMR for Organic Chemists
, pp. 89-91
-
-
Dolbier, W.R.Jr.1
-
67
-
-
78349273577
-
-
note
-
Crystals of 5c (transparent plate, colorless) were grown from the ether by slow evaporation. CCDC 775673 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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