-
1
-
-
34248211045
-
-
J. F. Briat, C. Curie, F. Gaymard, Curr. Opin. Plant Biol. 2007, 10, 276-282.
-
(2007)
Curr. Opin. Plant Biol.
, vol.10
, pp. 276-282
-
-
Briat, J.F.1
Curie, C.2
Gaymard, F.3
-
2
-
-
78650270004
-
-
http://library.thinkquest.org/C005921/Earth/eartSurf.htm.
-
-
-
-
4
-
-
84959955755
-
-
H. Marschner, V. Römheld, M. Kissel, J. Plant Nutr. 1986, 9, 695-713.
-
(1986)
J. Plant Nutr.
, vol.9
, pp. 695-713
-
-
Marschner, H.1
Römheld, V.2
Kissel, M.3
-
6
-
-
84969194850
-
-
T. Takemoto, K. Nomoto, S. Fushiya, R. Ouchi, H. Kusano, H. Hikino, S. Takagi, Y. Matsuura, M. Kakudo, Proc. Jpn. Acad. 1978, 54, 469-473.
-
(1978)
Proc. Jpn. Acad.
, vol.54
, pp. 469-473
-
-
Takemoto, T.1
Nomoto, K.2
Fushiya, S.3
Ouchi, R.4
Kusano, H.5
Hikino, H.6
Takagi, S.7
Matsuura, Y.8
Kakudo, M.9
-
8
-
-
33646240063
-
-
Y. Murata, J. F. Ma, N. Yamaji, D. Ueno, K. Nomoto, T. Iwashita, Plant J. 2006, 46, 563-572.
-
(2006)
Plant J.
, vol.46
, pp. 563-572
-
-
Murata, Y.1
Ma, J.F.2
Yamaji, N.3
Ueno, D.4
Nomoto, K.5
Iwashita, T.6
-
9
-
-
57749169737
-
-
C. Curie, G. Cassin, D. Couch, F. Divol, K. Higuchi, M. Lea Jean, J. Misson, A. Schikora, P. Czernic, S. Mari, Ann. Bot. 2009, 103, 1-11.
-
(2009)
Ann. Bot.
, vol.103
, pp. 1-11
-
-
Curie, C.1
Cassin, G.2
Couch, D.3
Divol, F.4
Higuchi, K.5
Lea Jean, M.6
Misson, J.7
Schikora, A.8
Czernic, P.9
Mari, S.10
-
10
-
-
34548124822
-
-
E. Harada, K. Sugase, K. Namba, T. Iwashita, Y. Murata, FEBS Lett. 2007, 581, 4298-4302.
-
(2007)
FEBS Lett.
, vol.581
, pp. 4298-4302
-
-
Harada, E.1
Sugase, K.2
Namba, K.3
Iwashita, T.4
Murata, Y.5
-
11
-
-
78650287447
-
-
K. Namba, Y. Murata, M. Horikawa, T. Iwashita, S. Kusumoto, Angew. Chem. 2007, 119, 7190-7193
-
(2007)
Angew. Chem.
, vol.119
, pp. 7190-7193
-
-
Namba, K.1
Murata, Y.2
Horikawa, M.3
Iwashita, T.4
Kusumoto, S.5
-
12
-
-
34848928102
-
-
Angew. Chem. Int. Ed. 2007, 46, 7060-7063.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 7060-7063
-
-
-
13
-
-
0035905794
-
-
C. Curie, Z. Panaviene, C. Loulergue, S. L. Dellaporta, J. F. Briat, E. L. Walker, Nature 2001, 409, 346-349.
-
(2001)
Nature
, vol.409
, pp. 346-349
-
-
Curie, C.1
Panaviene, Z.2
Loulergue, C.3
Dellaporta, S.L.4
Briat, J.F.5
Walker, E.L.6
-
14
-
-
78650266451
-
-
For previous syntheses of DMA and MA, see references cited in Ref.[11].
-
For previous syntheses of DMA and MA, see references cited in Ref.[11].
-
-
-
-
15
-
-
0027267822
-
-
Nucleophilic substitution was not attempted because of concern that the activation of the 2′-hydroxy group would induce βa elimination (see:).
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Nucleophilic substitution was not attempted because of concern that the activation of the 2′-hydroxy group would induce βa elimination (see:, F. Matsuura, Y. Hamada, T. Shioiri, Tetrahedron 1993, 49, 8211-8222).
-
(1993)
Tetrahedron
, vol.49
, pp. 8211-8222
-
-
Matsuura, F.1
Hamada, Y.2
Shioiri, T.3
-
16
-
-
78650261822
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note
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The click reaction of benzyl azide and 1-hexyne in the presence of CuI (1a mol%) and 14a (1a mol%) afforded the desired 1,2,3-triazole in 95% yield. In contrast, treatment with only CuI (1a mol%) in the absence of 14a gave the 1,2,3-triazole in less than 20% yield, and the starting materials were recovered.
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17
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1542305429
-
-
G. Schaaf, U. Ludewig, B. E. Erenoglu, S. Mori, T. Kitahara, N. vona Wierén, J. Biol. Chem. 2004, 279, 9091-9096.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 9091-9096
-
-
Schaaf, G.1
Ludewig, U.2
Erenoglu, B.E.3
Mori, S.4
Kitahara, T.5
Vona Wierén, N.6
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18
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9144248315
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A suitably substituted 1,2,4-triazole derivative was reported to behave as an effective metal chelator
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A suitably substituted 1,2,4-triazole derivative was reported to behave as an effective metal chelator:, U. Heinz, K. Hegetschweiler, P. Acklin, B. Faller, R. Lattman, H. P. Schnebli, Angew. Chem. 1999, 111, 2733-2736
-
(1999)
Angew. Chem.
, vol.111
, pp. 2733-2736
-
-
Heinz, U.1
Hegetschweiler, K.2
Acklin, P.3
Faller, B.4
Lattman, R.5
Schnebli, H.P.6
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19
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0033520468
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the case of our MA derivatives 15, by contrast, the simple 1,2,3-triazole ring is not expected to disturb the strong effect of the multivalent coordination of the MA part of these compounds.
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Angew. Chem. Int. Ed. 1999, 38, 2568-2570. In the case of our MA derivatives 15, by contrast, the simple 1,2,3-triazole ring is not expected to disturb the strong effect of the multivalent coordination of the MA part of these compounds.
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 2568-2570
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