-
2
-
-
0344862912
-
-
Pandit, U.K.; Grose, W.F.A.; Eggelte, T.A. Synth. Commun. 1972, 2, 345-351.
-
(1972)
Synth. Commun.
, vol.2
, pp. 345-351
-
-
Pandit, U.K.1
Grose, W.F.A.2
Eggelte, T.A.3
-
4
-
-
0023259332
-
-
(b) Harnden, M.R.; Jarvest, R.L.; Bacon, T.H.; Boyd, M.R. J. Med. Chem. 1987, 30, 1636-1642;
-
(1987)
J. Med. Chem.
, vol.30
, pp. 1636-1642
-
-
Harnden, M.R.1
Jarvest, R.L.2
Bacon, T.H.3
Boyd, M.R.4
-
5
-
-
0021672102
-
-
(c) Tippie, M.A.; Martin, J.C.; Smee, D.F.; Matthews, T.R.; Verheyden, J.P.H. Nucleosides Nucleotides 1984, 3, 525-535;
-
(1984)
Nucleosides Nucleotides
, vol.3
, pp. 525-535
-
-
Tippie, M.A.1
Martin, J.C.2
Smee, D.F.3
Matthews, T.R.4
Verheyden, J.P.H.5
-
6
-
-
0024463519
-
-
(d) Hannah, J.; Tolman, R.L.; Karkas, J.D.; Liou, R.; Perry, H.C.; Field, A.K. J. Heterocyclic Chem. 1989, 26, 1261-1271;
-
(1989)
Heterocyclic Chem.
, vol.26
, pp. 1261-1271
-
-
Hannah, J.1
Tolman, R.L.2
Karkas, J.D.3
Liou, R.4
Perry, H.C.5
Field, A.K.J.6
-
7
-
-
0028231795
-
-
(e) Choudary, B.M.; Geen, G.R.; Grinter, T.J.; MacBeath, F.S.; Parratt, M.J. Nucleosides Nucleotides 1994, 13, 979-996;
-
(1994)
Nucleosides Nucleotides
, vol.13
, pp. 979-996
-
-
Choudary, B.M.1
Geen, G.R.2
Grinter, T.J.3
MacBeath, F.S.4
Parratt, M.J.5
-
8
-
-
0029985688
-
-
(f) Choudary, B.M.; Geen, G.R.; Kincey, P.M.; Parratt, M.J.; Dales, J.R.M.; Johnson, G.P.; O'Donnell, S.; Tudor, D.W.; Woods, N. Nucleosides Nucleotides 1996, 15, 981-994;
-
(1996)
Nucleosides Nucleotides
, vol.15
, pp. 981-994
-
-
Choudary, B.M.1
Geen, G.R.2
Kincey, P.M.3
Parratt, M.J.4
Dales, J.R.M.5
Johnson, G.P.6
O'Donnell, S.7
Tudor, D.W.8
Woods, N.9
-
9
-
-
0033574677
-
-
(g) Brand, B.; Reese, C.B.; Song, Q.; Visintin, C. Tetrahedron 1999, 55, 5239-5252;
-
(1999)
Tetrahedron
, vol.55
, pp. 5239-5252
-
-
Brand, B.1
Reese, C.B.2
Song, Q.3
Visintin, C.4
-
10
-
-
0035951956
-
-
(h) Geen, G.R.; Kincey, P.M.; Spoors, P.G. Tetrahedron Lett. 2001, 42, 1781-1784.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 1781-1784
-
-
Geen, G.R.1
Kincey, P.M.2
Spoors, P.G.3
-
11
-
-
0034048929
-
-
For example see: (a) Gambhir, S.S.; Herschman, H.R.; Cherry, S.R.; Barrio, J.R.; Satyamurthy, N.; Toyokuni, T.; Phelps, M.E.; Larson, S.M.; Balatoni, J.; Finn, R.; Sadelain, M.; Tjuvajev, J.; Blasberg, R. Neoplasia 2000, 2, 118-138;
-
(2000)
Neoplasia
, vol.2
, pp. 118-138
-
-
Gambhir, S.S.1
Herschman, H.R.2
Cherry, S.R.3
Barrio, J.R.4
Satyamurthy, N.5
Toyokuni, T.6
Phelps, M.E.7
Larson, S.M.8
Balatoni, J.9
Finn, R.10
Sadelain, M.11
Tjuvajev, J.12
Blasberg, R.13
-
12
-
-
0033625192
-
-
(b) Namavari, M.; Barrio, J.R.; Toyokuni, T.; Gambhir, S.S.; Cherry, S.R.; Herschman, H.R.; Phelps, M.E.; Satyamurthy. N. Nucl. Med. Biol. 2000, 27, 157-162;
-
(2000)
Satyamurthy. N. Nucl. Med. Biol.
, vol.27
, pp. 157-162
-
-
Namavari, M.1
Barrio, J.R.2
Toyokuni, T.3
Gambhir, S.S.4
Cherry, S.R.5
Herschman, H.R.6
Phelps, M.E.7
-
13
-
-
0034898675
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-
(c) Yaghoubi, S.; Barrio, J.R.; Dahlbom, M.; Iyer, M.; Namavari, M.; Satyamurthy, N.; Goldman, R.; Herschman, H.R.; Phelps, M.E.; Gambhir, S.S. J. Nucl. Med. 2001, 42, 1225-1234.
-
(2001)
Nucl. Med.
, vol.42
, pp. 1225-1234
-
-
Yaghoubi, S.1
Barrio, J.R.2
Dahlbom, M.3
Iyer, M.4
Namavari, M.5
Satyamurthy, N.6
Goldman, R.7
Herschman, H.R.8
Phelps, M.E.9
Gambhir, S.S.J.10
-
14
-
-
0001480434
-
-
Soai, K.; Oyamada, H.; Ookawa, A. Synth. Commun. 1982, 12, 463-467.
-
(1982)
Synth. Commun.
, vol.12
, pp. 463-467
-
-
Soai, K.1
Oyamada, H.2
Ookawa, A.3
-
15
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0345492504
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-
WO Patent 9,944,976, Sep. 10, 1999
-
Removal of borate by an anion-exchange resin has been reported. See: Ikai, K.; Mikami, M.; Furukawa, Y.; Ho, S. WO Patent 9,944,976, Sep. 10, 1999.
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-
-
Ikai, K.1
Mikami, M.2
Furukawa, Y.3
Ho, S.4
-
16
-
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0003463148
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-
John Wiley & Sons, Inc.: New York
-
For example see: (a) Greene, T.W.; Wuts, P.G.M. Protective Groups in Organic Synthesis, 3rd Ed.; John Wiley & Sons, Inc.: New York, 1999; 217-224;
-
(1999)
Protective Groups in Organic Synthesis, 3rd Ed.
, pp. 217-224
-
-
Greene, T.W.1
Wuts, P.G.M.2
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18
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0344630367
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JP Patent 11,158,174, June 15, 1999
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The compound 12 was previously prepared by the reaction of 3 with benzaldehyde in the presence of TsOH via constant removal of water by azeotropic distillation with toluene at 80°C. See: Hamazaki, T.; Agehara, K.; Onishi, T.; Iwasaki, H. JP Patent 11,158,174, June 15, 1999.
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Hamazaki, T.1
Agehara, K.2
Onishi, T.3
Iwasaki, H.4
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19
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0345060952
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note
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A similar isomerization was reported during the transformation of 7 to 8 through the corresponding mesylate (see Ref. 3e).
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20
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0344630368
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note
-
We have been carrying out this coupling reaction during a weekend. Harnden et al. reported that 6 and 9 were reacted at 4°C overnight, while Geen et al. left the mixture of 8 and 9 at room temperature for 18 h (see Ref. 3b and Ref. 3e, respectively).
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