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7
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0343007531
-
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note
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Other important 2,3,6-trideoxysugars present in angucycline antibiotics are L-aculose, L-cinerulose, D-kerriose, D-amicetose and D-rhodinose.
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12
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0343443204
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Section 2
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An excellent review, describing the factors which are important for cooperative effects in biological systems, was published by:
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An excellent review, describing the factors which are important for cooperative effects in biological systems, was published by: Mammen, M.; Choi, S. K.; Whitesides, G. M. Angew. Chem. 1998, 110, 2908; Angew. Chem., Int. Ed. Engl. 1998, 37, 2754.
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Mammen, M.1
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An excellent review, describing the factors which are important for cooperative effects in biological systems, was published by: Mammen, M.; Choi, S. K.; Whitesides, G. M. Angew. Chem. 1998, 110, 2908; Angew. Chem., Int. Ed. Engl. 1998, 37, 2754.
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(d) Rodriguez, M. J.; Snyder, N. J.; Zweifel, M. J.; Wilkie, S. C.; Stack, D. R.; Cooper, R. D.; Nicas, T. I.; Mullen, D. L.; Butler, T. F.; Thompson, R. C. J. Antibiotics 1998, 51, 560.
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Mullen, D.L.8
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22
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0030056863
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Elegant total syntheses of angucycline antibiotics: (a)
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Elegant total syntheses of angucycline antibiotics: (a) Matsuo, G.; Miki, Y.; Nakata, M.; Matsumura, S.; Toshima, K. J. Chem. Soc., Chem. Commun. 1996, 225.
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(b) Matsumoto, T.; Sohma, T.; Yamaguchi, H.; Kurata, S.; Suzuki, K. Synlett 1995, 263.
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Matsumoto, T.1
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24
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0001203902
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(c) Kim, K.; Sulikowski, G. A. Angew. Chem. 1995, 107, 2587; Angew. Chem., Int. Ed. Engl. 1995, 34, 2396.
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(c) Kim, K.; Sulikowski, G. A. Angew. Chem. 1995, 107, 2587; Angew. Chem., Int. Ed. Engl. 1995, 34, 2396.
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0028091240
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Couplings of glycals with anthracyclinones have been studied by: (a)
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Couplings of glycals with anthracyclinones have been studied by: (a) Roche, C. J.; Berkowitz, D.; Sulikowski, G. A.; Danishefsky, S. J.; Crothers, D. M. Biochemistry 1994, 33, 936.
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(a) Danishefsky, S. J.; Bilodeau, M. T. Angew. Chem. 1996, 108, 1482; Angew. Chem., Int. Ed. Engl. 1996, 35, 1380.
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(a) Danishefsky, S. J.; Bilodeau, M. T. Angew. Chem. 1996, 108, 1482; Angew. Chem., Int. Ed. Engl. 1996, 35, 1380.
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(a) Drautz, H.; Zähner, H.; Rohr, J.; Zeeck, A. J. Antibiot. 1986, 39, 1657.
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39
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0343007527
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PhD dissertation, University of Göttingen
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Rohr, J., PhD dissertation, University of Göttingen 1984.
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(1984)
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Rohr, J.1
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40
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0343443201
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note
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2:MeOH 9:1 then Sephadex: MeOH, pH 7).
-
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42
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25344459573
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PhD dissertation, TU Clausthal
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Dräger, G., PhD dissertation, TU Clausthal 1997.
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(1997)
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Dräger, G.1
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43
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0029120877
-
-
The preparation of both enantiomers of 10 has been reported in refs 8a and e and in:
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The preparation of both enantiomers of 10 has been reported in refs 8a and e and in: Boyd, V. A.; Sulikowski, G. A. J. Am. Chem. Soc. 1995, 117, 8472.
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Boyd, V.A.1
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Toshima, K.1
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48
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33751141247
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Tietze, L. F.; Hannemann, R.; Buhr, W.; Lögers, M.; Menningen, P.; Lieb, M.; Starck, D.; Grote, T.; Döring, A.; Schuberth, I. Angew. Chem. 1996, 108, 2840; Angew. Chem., Int. Ed. Engl. 1996, 35, 2674.
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Tietze, L.F.1
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Schuberth, I.10
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49
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33751141247
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Tietze, L. F.; Hannemann, R.; Buhr, W.; Lögers, M.; Menningen, P.; Lieb, M.; Starck, D.; Grote, T.; Döring, A.; Schuberth, I. Angew. Chem. 1996, 108, 2840; Angew. Chem., Int. Ed. Engl. 1996, 35, 2674.
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-
-
50
-
-
0343443199
-
-
50 is determined as the effective dose giving 50% growth inhibition
-
50 is determined as the effective dose giving 50% growth inhibition.
-
-
-
-
51
-
-
0343007523
-
-
The tests have been conducted at the Hans-Knöll-Institut in Jena, Germany
-
The tests have been conducted at the Hans-Knöll-Institut in Jena, Germany.
-
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52
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85046499153
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Härtl A., Stelzner A., Ritzau M., Heinze S., Gräfe U. J. Antibiotics. 51:1998;528.
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Härtl, A.1
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Heinze, S.4
Gräfe, U.5
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53
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25344460974
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(Hans-Knöll-Institut in Jena, Germany), private communication
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Härtl, A.; Sattler, I. (Hans-Knöll-Institut in Jena, Germany), private communication.
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-
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Härtl, A.1
Sattler, I.2
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