-
5
-
-
0033799849
-
-
Higashibayashi, S.; Shinko, K.; Ishizu, T.; Hashimoto, K.; Shirahama, H.; Nakata, M. Synlett 2000, 9, 1306-1308
-
(2000)
Synlett
, vol.9
, pp. 1306-1308
-
-
Higashibayashi, S.1
Shinko, K.2
Ishizu, T.3
Hashimoto, K.4
Shirahama, H.5
Nakata, M.6
-
7
-
-
77956521269
-
-
Wang, J. T.; Wu, W. T.; Xu, Y. F.; Wu, L. M. Chin. Sci. Bull. 2010, 55, 2803-2806).
-
(2010)
Chin. Sci. Bull.
, vol.55
, pp. 2803-2806
-
-
Wang, J.T.1
Wu, W.T.2
Xu, Y.F.3
Wu, L.M.4
-
9
-
-
0027446641
-
-
Hogrefe, R. I.; McCaffrey, A. P.; Borozdina, L. U.; McCampbell, E. S.; Vaghefi, M. M. Nucleic Acids Res. 1993, 21, 4739-4741
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 4739-4741
-
-
Hogrefe, R.I.1
McCaffrey, A.P.2
Borozdina, L.U.3
McCampbell, E.S.4
Vaghefi, M.M.5
-
10
-
-
33845470265
-
-
Cox, D. P.; Terpinski, J.; Lawrynowicz, W. J. Org. Chem. 1984, 49, 3216-3219
-
(1984)
J. Org. Chem.
, vol.49
, pp. 3216-3219
-
-
Cox, D.P.1
Terpinski, J.2
Lawrynowicz, W.3
-
11
-
-
33746892455
-
-
Pilcher, A. S.; Ammon, P.; DeShong, P. J. Am. Chem. Soc. 1995, 117, 5166-5167
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5166-5167
-
-
Pilcher, A.S.1
Ammon, P.2
Deshong, P.3
-
12
-
-
60149092468
-
-
Wu, X.; Zhou, J.; Snider, B. B. Angew Chem., Int. Ed. 2009, 48, 1283-1286
-
(2009)
Angew Chem., Int. Ed.
, vol.48
, pp. 1283-1286
-
-
Wu, X.1
Zhou, J.2
Snider, B.B.3
-
13
-
-
73149104665
-
-
Siegel, D. S.; Piizi, G.; Piersanti, G.; Movassaghi, M. J. Org. Chem. 2009, 74, 9292-9304
-
(2009)
J. Org. Chem.
, vol.74
, pp. 9292-9304
-
-
Siegel, D.S.1
Piizi, G.2
Piersanti, G.3
Movassaghi, M.4
-
15
-
-
0001409192
-
-
Scheidt, K. A.; Chen, H.; Follows, B. C.; Chemler, S. R.; Coffey, D. S.; Roush, W. R. J. Org. Chem. 1998, 63, 6436-6437
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6436-6437
-
-
Scheidt, K.A.1
Chen, H.2
Follows, B.C.3
Chemler, S.R.4
Coffey, D.S.5
Roush, W.R.6
-
16
-
-
78449265566
-
-
Burke, C. P.; Swingle, M. R.; Honkanen, R. E.; Boger, D. L. J. Org. Chem. 2010, 75, 7505-7513
-
(2010)
J. Org. Chem.
, vol.75
, pp. 7505-7513
-
-
Burke, C.P.1
Swingle, M.R.2
Honkanen, R.E.3
Boger, D.L.4
-
17
-
-
79955899426
-
-
Herzon, S. B.; Lu, L.; Woo, C. M.; Gholap, S. L. J. Am. Chem. Soc. 2011, 133, 7260-7263
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 7260-7263
-
-
Herzon, S.B.1
Lu, L.2
Woo, C.M.3
Gholap, S.L.4
-
18
-
-
80052710487
-
-
Kim, D. W.; Jeong, H-J.; Lim, S. T.; Sohn, M.-H. Angew. Chem. 2008, 120, 8352-8354
-
(2008)
Angew. Chem.
, vol.120
, pp. 8352-8354
-
-
Kim, D.W.1
Jeong, H.-J.2
Lim, S.T.3
Sohn, M.-H.4
-
19
-
-
78149313480
-
-
Coombs, T. C.; Huang, W.; Garnier-Amblard, E. C.; Liebeskind, L. S. Organometallics. 2010, 29, 5083-5097
-
(2010)
Organometallics.
, vol.29
, pp. 5083-5097
-
-
Coombs, T.C.1
Huang, W.2
Garnier-Amblard, E.C.3
Liebeskind, L.S.4
-
22
-
-
0026567054
-
-
4F (14 equiv) in MeOH (60 °C) (;). The deprotection conditions described herein differ from the method of Zhang and Robins in several ways: the conditions reported herein (i) use catalytic quantities of fluoride, (ii) operate at room temperature, and (iii) provide control over the pH of the reaction mixture.
-
4F (14 equiv) in MeOH (60 °C) (Zhang, W.; Robins, M. J. Tetrahedron Lett. 1992, 33, 1177-1180). The deprotection conditions described herein differ from the method of Zhang and Robins in several ways: the conditions reported herein (i) use catalytic quantities of fluoride, (ii) operate at room temperature, and (iii) provide control over the pH of the reaction mixture.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 1177-1180
-
-
Zhang, W.1
Robins, M.J.2
-
23
-
-
84985155009
-
-
Oppolzer, W.; Snowden, R. L.; Simmons, D. P. Helv. Chem. Acta 1981, 64, 2002-2021
-
(1981)
Helv. Chem. Acta
, vol.64
, pp. 2002-2021
-
-
Oppolzer, W.1
Snowden, R.L.2
Simmons, D.P.3
-
26
-
-
0000877512
-
-
Denmark, S E.; Hammer, R. P.; Weber, E. J.; Habermas, K. L. J. Org. Chem. 1987, 52, 165-168
-
(1987)
J. Org. Chem.
, vol.52
, pp. 165-168
-
-
Denmark, S.E.1
Hammer, R.P.2
Weber, E.J.3
Habermas, K.L.4
-
27
-
-
0001117875
-
-
The stability of the FMOC protecting group under the reaction conditions is especially interesting, as unbuffered TBAF has been used by Ueki and Amemiya to rapidly deprotect FMOC protected amines
-
The stability of the FMOC protecting group under the reaction conditions is especially interesting, as unbuffered TBAF has been used by Ueki and Amemiya to rapidly deprotect FMOC protected amines: Ueki, M.; Amemiya, M. Tetrahedron Lett. 1987, 28, 6617-6620
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 6617-6620
-
-
Ueki, M.1
Amemiya, M.2
-
28
-
-
0000081048
-
-
3SiOH byproducts that must be removed by chromatography.
-
3SiOH byproducts that must be removed by chromatography.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 6071-6073
-
-
Cirillo, P.F.1
Panek, J.S.2
-
30
-
-
0000852004
-
-
Corriu, R. J. P.; Moreau, J. J.; Pataud-Sat, M. J. Org. Chem. 1990, 55, 2878-2884
-
(1990)
J. Org. Chem.
, vol.55
, pp. 2878-2884
-
-
Corriu, R.J.P.1
Moreau, J.J.2
Pataud-Sat, M.3
-
31
-
-
0002714675
-
-
Still, W. C.; Kahn, M.; Mitra, A. J. Org. Chem. 1978, 43, 2923-2925
-
(1978)
J. Org. Chem.
, vol.43
, pp. 2923-2925
-
-
Still, W.C.1
Kahn, M.2
Mitra, A.3
-
32
-
-
66149142790
-
-
Campo, V. L.; Martins, M. B.; da Silva, C. H. T. P.; Carvalho, I. Tetrahedron 2009, 65, 5343-5349
-
(2009)
Tetrahedron
, vol.65
, pp. 5343-5349
-
-
Campo, V.L.1
Martins, M.B.2
Da Silva, C.H.T.P.3
Carvalho, I.4
-
33
-
-
0033150474
-
-
Feldman, K. S.; Mingo, P. A.; Hawkins, P. C. D. Heterocycles 1999, 51, 1283-1294
-
(1999)
Heterocycles
, vol.51
, pp. 1283-1294
-
-
Feldman, K.S.1
Mingo, P.A.2
Hawkins, P.C.D.3
-
34
-
-
0001574187
-
-
Tanner, D. D.; Diaz, G. E.; Potter, A. J. Org. Chem. 1985, 50, 2149-2154
-
(1985)
J. Org. Chem.
, vol.50
, pp. 2149-2154
-
-
Tanner, D.D.1
Diaz, G.E.2
Potter, A.3
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