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1
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85030918137
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Boston, MA, American Chemical Society: Washington, DC, 18-22 August; MED 209
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Naidu, B. N.; Sorenson, M. E.; Connolly, T. P.; Wichtowski, J. A.; Ueda, Y.; Bronson, J. J.; Zhang, Y.; Kim, O.; Li, W.; Lam, K. S.; Pucci, M. J.; Clark, J. M.; Warr, G. A.; DenBleyker, K. L.; Stickle, T. M.; Taylor, D.; Lamb, L. M. ; Medina, I. A.; Macci, R.; Venkatesh, S.; Fung, L.; Alberts, J. Abstracts of Papers, 224th National Meeting of American Chemical Society, Boston, MA, American Chemical Society: Washington, DC, 18-22 August 2002; MED 209.
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(2002)
Abstracts of Papers, 224th National Meeting of American Chemical Society
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Naidu, B.N.1
Sorenson, M.E.2
Connolly, T.P.3
Wichtowski, J.A.4
Ueda, Y.5
Bronson, J.J.6
Zhang, Y.7
Kim, O.8
Li, W.9
Lam, K.S.10
Pucci, M.J.11
Clark, J.M.12
Warr, G.A.13
DenBleyker, K.L.14
Stickle, T.M.15
Taylor, D.16
Lamb, L.M.17
Medina, I.A.18
Macci, R.19
Venkatesh, S.20
Fung, L.21
Alberts, J.22
more..
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2
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0037361644
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Li W., Leet J.E., Ax H.A., Gustavson D.R., Brown D.M., Turner L., Brown K., Clark J., Yang H., Fung-Tomc J., Lam K.S. J. Antibiot. 56:2003;226-231.
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J. Antibiot.
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Li, W.1
Leet, J.E.2
Ax, H.A.3
Gustavson, D.R.4
Brown, D.M.5
Turner, L.6
Brown, K.7
Clark, J.8
Yang, H.9
Fung-Tomc, J.10
Lam, K.S.11
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3
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0037363218
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Leet J.E., Li W., Ax H.A., Matson J.A., Huang S., Huang R., Cantone J.L., Drexler D., Dalterio R.A., Lam K.S. J. Antibiot. 56:2003;232-242.
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(2003)
J. Antibiot.
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Leet, J.E.1
Li, W.2
Ax, H.A.3
Matson, J.A.4
Huang, S.5
Huang, R.6
Cantone, J.L.7
Drexler, D.8
Dalterio, R.A.9
Lam, K.S.10
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4
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0031664946
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Sasaki T., Otani T., Matsumoto H., Unemi N., Hamada M., Takeuchi T., Hori M. J. Antibiot. 8:1998;715-721.
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(1998)
J. Antibiot.
, vol.8
, pp. 715-721
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Sasaki, T.1
Otani, T.2
Matsumoto, H.3
Unemi, N.4
Hamada, M.5
Takeuchi, T.6
Hori, M.7
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5
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0037178105
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Constantine K.L., Mueller L., Huang S., Abid S., Lam K.S., Li W., Leet J.E. J. Am. Chem. Soc. 124:2002;7284-7285.
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(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 7284-7285
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Constantine, K.L.1
Mueller, L.2
Huang, S.3
Abid, S.4
Lam, K.S.5
Li, W.6
Leet, J.E.7
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6
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0037073954
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For another example, see
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For another example, see Hrnciar P., Ueda Y., Huang S., Leet J.E., Bronson J.J. J. Org. Chem. 67:2002;8789-8793.
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(2002)
J. Org. Chem.
, vol.67
, pp. 8789-8793
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Hrnciar, P.1
Ueda, Y.2
Huang, S.3
Leet, J.E.4
Bronson, J.J.5
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11
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0035544082
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and references cited therein
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Ferreira P.M.T., Maia H.L.S., Monteiro L.S., Sacramento J. J. Chem. Soc., Perkin Trans. 1. 2001;3167-3173. and references cited therein.
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(2001)
J. Chem. Soc., Perkin Trans. 1
, pp. 3167-3173
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Ferreira, P.M.T.1
Maia, H.L.S.2
Monteiro, L.S.3
Sacramento, J.4
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12
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0006143391
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and references cited therein
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Sanui K., Ogata N. Bull. Chem. Soc. Jpn. 41:1968;1968-1970. and references cited therein.
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(1968)
Bull. Chem. Soc. Jpn.
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Sanui, K.1
Ogata, N.2
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14
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0346618112
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Chem. Abstr. 64:1966;3589.
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(1966)
Chem. Abstr.
, vol.64
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15
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85030924887
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note
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2b and that of morpholine and triethylamine are 8.3 and 11.0, respectively. The homogeneous aqueous solution obtained from nocathiacin I and 10 equiv morpholine has pH of ~9. We speculate that under the reaction conditions nocathiacin I predominantly exists in a deprotonated form.
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16
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0004252595
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P.A. Grieco. London: Blackie Academic and Professional
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Grieco P.A. Organic Synthesis in Water. 1998;Blackie Academic and Professional, London.
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(1998)
Organic Synthesis in Water
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21
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0030597022
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Jenner G. Tetrahedron. 52:1996;13557-13568.
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(1996)
Tetrahedron
, vol.52
, pp. 13557-13568
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Jenner, G.1
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26
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85030918135
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in press. (Web release date 27 November 2003)
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For Michael addition of amines and thiols to simple dehydroalanine amides, see Naidu, B. N.; Sorenson, M. E.; Connolly, T. P.; Ueda, Y. J. Org. Chem., in press. (Web release date 27 November 2003).
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J. Org. Chem.
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Naidu, B.N.1
Sorenson, M.E.2
Connolly, T.P.3
Ueda, Y.4
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28
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85030932502
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note
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2O: C, 45.38; H, 4.87; N, 12.21; S, 9.32; Cl, 5.15; found: C, 45.11; H, 4.71; N, 12.15; S, 9.25; Cl, 5.19.
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29
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85030934687
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Reactions were run using 0.1 mmol of 1 in 1 mL of de-ionized water
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Reactions were run using 0.1 mmol of 1 in 1 mL of de-ionized water.
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30
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85030930423
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The reaction was run using 5 mmol of 3 in 10 mL of de-ionozed water
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The reaction was run using 5 mmol of 3 in 10 mL of de-ionozed water.
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