-
1
-
-
0642383074
-
-
Ed.: H. Scheer, CRC, Boca Raton
-
G.A.F. Hendry, J. D. Houghton, S. B. Brown in Chlorophylls (Ed.: H. Scheer), CRC, Boca Raton, 1991, p. 465.
-
(1991)
Chlorophylls
, pp. 465
-
-
Hendry, G.A.F.1
Houghton, J.D.2
Brown, S.B.3
-
3
-
-
85024610803
-
-
K. H. Bortlik, C. Peisker, P. Matile, J. Plant Physiol. 1990, 136, 161-165.
-
(1990)
J. Plant Physiol.
, vol.136
, pp. 161-165
-
-
Bortlik, K.H.1
Peisker, C.2
Matile, P.3
-
4
-
-
0001307755
-
-
a) B. Kräutler, B. Jaun, K. Bortlik, M. Schellenberg, P. Matile, Angew. Chem. 1991, 103, 1354-1357; Angew. Chem. Int. Ed. Engl. 1991, 30, 1315-1318;
-
(1991)
Angew. Chem.
, vol.103
, pp. 1354-1357
-
-
Kräutler, B.1
Jaun, B.2
Bortlik, K.3
Schellenberg, M.4
Matile, P.5
-
5
-
-
33748598147
-
-
a) B. Kräutler, B. Jaun, K. Bortlik, M. Schellenberg, P. Matile, Angew. Chem. 1991, 103, 1354-1357; Angew. Chem. Int. Ed. Engl. 1991, 30, 1315-1318;
-
(1991)
Angew. Chem. Int. Ed. Engl.
, vol.30
, pp. 1315-1318
-
-
-
6
-
-
0001128670
-
-
b) B. Kräutler, B. Jaun, W. Amrein, K. Bortlik, M. Schellenberg, P. Matile, Plant Physiol. Biochem. 1992, 30, 333-346.
-
(1992)
Plant Physiol. Biochem.
, vol.30
, pp. 333-346
-
-
Kräutler, B.1
Jaun, B.2
Amrein, W.3
Bortlik, K.4
Schellenberg, M.5
Matile, P.6
-
7
-
-
0027724750
-
-
a) W. Mühlecker, B. Kräutler, S. Ginsburg, P. Matile, Helv. Chim. Acta, 1993, 76, 2976-2980;
-
(1993)
Helv. Chim. Acta
, vol.76
, pp. 2976-2980
-
-
Mühlecker, W.1
Kräutler, B.2
Ginsburg, S.3
Matile, P.4
-
9
-
-
0000627098
-
-
J. Iturraspe, N. Moyano, B. Frydman, J. Org. Chem. 1995, 60, 6664-6665.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 6664-6665
-
-
Iturraspe, J.1
Moyano, N.2
Frydman, B.3
-
11
-
-
0029107117
-
-
S. Hörtensteiner, F. Vicentini, P. Matile, New Phytol. 1995, 129, 237-246
-
(1995)
New Phytol.
, vol.129
, pp. 237-246
-
-
Hörtensteiner, S.1
Vicentini, F.2
Matile, P.3
-
12
-
-
0028042227
-
-
a) S. Ginsburg, M. Schellenberg, P. Matile, Plant Physiol. 1994, 105, 545-554;
-
(1994)
Plant Physiol.
, vol.105
, pp. 545-554
-
-
Ginsburg, S.1
Schellenberg, M.2
Matile, P.3
-
13
-
-
0027995730
-
-
b) A. Bachmann, S. Fernández-López, S. Ginsburg, H. Thomas, J. C. Bouwkamp, T. Solomos, P. Matile, New Phytol. 1994, 126, 593-600.
-
(1994)
New Phytol.
, vol.126
, pp. 593-600
-
-
Bachmann, A.1
Fernández-López, S.2
Ginsburg, S.3
Thomas, H.4
Bouwkamp, J.C.5
Solomos, T.6
Matile, P.7
-
14
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0642352545
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note
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max/min (rel. Δε) = 360 (sh, 0.60), 328 (1.00), 282 (-0.50), 238 (-0.67), 205 nm(-1.65).
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16
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0001202977
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-
a) H. Kessler, M. Gehrke, C. Griesinger, Angew. Chem. 1988, 100, 507-554; Angew. Chem. Int. Ed. Engl. 1988, 27, 490-537;
-
(1988)
Angew. Chem.
, vol.100
, pp. 507-554
-
-
Kessler, H.1
Gehrke, M.2
Griesinger, C.3
-
17
-
-
84990113699
-
-
a) H. Kessler, M. Gehrke, C. Griesinger, Angew. Chem. 1988, 100, 507-554; Angew. Chem. Int. Ed. Engl. 1988, 27, 490-537;
-
(1988)
Angew. Chem. Int. Ed. Engl.
, vol.27
, pp. 490-537
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-
20
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0642352544
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note
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2O (9/1, v/v). Bn-FCC-2 from rape cotyledons was compared to 3 by means of analytical HPLC (see ref. [9a]), UV/Vis-spectroscopy, and luminescence properties.
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21
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0002532549
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Experiments by Eschenmoser and co-workers provided evidence of favorable thermodynamics for the formation of pyrrole units in tautomerization reactions of (metal-free) hydroporphyrins: A. Eschenmoser, Angew. Chem. 1988, 100, 5-40; Angew. Chem. Int. Ed. Engl. 1988, 27, 5-40. The feasibility of the tautomerization of a mixture of 4,5-seco-4,5-dioxooctahydrophytoporphyrinates related to 3 to linear tetrapyrroles structurally similar to 1 has recently been reported: N. Engel, C. Curty, A. Gossauer, Plant Physiol. Biochem. 1996, 34, 77-83.
-
(1988)
Angew. Chem.
, vol.100
, pp. 5-40
-
-
Eschenmoser, A.1
-
22
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0011026647
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Experiments by Eschenmoser and co-workers provided evidence of favorable thermodynamics for the formation of pyrrole units in tautomerization reactions of (metal-free) hydroporphyrins: A. Eschenmoser, Angew. Chem. 1988, 100, 5-40; Angew. Chem. Int. Ed. Engl. 1988, 27, 5-40. The feasibility of the tautomerization of a mixture of 4,5-seco-4,5-dioxooctahydrophytoporphyrinates related to 3 to linear tetrapyrroles structurally similar to 1 has recently been reported: N. Engel, C. Curty, A. Gossauer, Plant Physiol. Biochem. 1996, 34, 77-83.
-
(1988)
Angew. Chem. Int. Ed. Engl.
, vol.27
, pp. 5-40
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-
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23
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0002371956
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Experiments by Eschenmoser and co-workers provided evidence of favorable thermodynamics for the formation of pyrrole units in tautomerization reactions of (metal-free) hydroporphyrins: A. Eschenmoser, Angew. Chem. 1988, 100, 5-40; Angew. Chem. Int. Ed. Engl. 1988, 27, 5-40. The feasibility of the tautomerization of a mixture of 4,5-seco-4,5-dioxooctahydrophytoporphyrinates related to 3 to linear tetrapyrroles structurally similar to 1 has recently been reported: N. Engel, C. Curty, A. Gossauer, Plant Physiol. Biochem. 1996, 34, 77-83.
-
(1996)
Plant Physiol. Biochem.
, vol.34
, pp. 77-83
-
-
Engel, N.1
Curty, C.2
Gossauer, A.3
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24
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0642321691
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note
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2 position (as in Bn-FCC-2, 3). Accordingly, in contrast to a recent proposal by Gossauer & Engel [17 b], there is no indication of an "early" hydrolysis of this ester function occurring during the chlorphyll breakdown in plants.
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25
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0028041797
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a) J. Iturraspe, N. Engel, A. Gossauer, Photochemistry 1994, 35, 1387-1390;
-
(1994)
Photochemistry
, vol.35
, pp. 1387-1390
-
-
Iturraspe, J.1
Engel, N.2
Gossauer, A.3
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27
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0028937273
-
-
C. Curty, N. Engel, A. Gossauer, FEBS Lett. 1995, 364, 41-44.
-
(1995)
FEBS Lett.
, vol.364
, pp. 41-44
-
-
Curty, C.1
Engel, N.2
Gossauer, A.3
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