-
1
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-
0037326264
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-
For reviews of our previous synthetic and biosynthetic work concerning this class of alkaloids, see: a
-
For reviews of our previous synthetic and biosynthetic work concerning this class of alkaloids, see: a) R. M. Williams, R. J. Cox, Acc. Chem. Res. 2003, 36, 127-139;
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(2003)
Acc. Chem. Res
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Williams, R.M.1
Cox, R.J.2
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3
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0035908153
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For representative studies on the biosynthesis of these types of alkaloids, see: a
-
For representative studies on the biosynthesis of these types of alkaloids, see: a) E. M. Stocking, J. F. Sanz-Cervera, C. J. Unkefer, R. M. Williams, Tetrahedron 2001, 57, 5303-5320;
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(2001)
Tetrahedron
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Stocking, E.M.1
Sanz-Cervera, J.F.2
Unkefer, C.J.3
Williams, R.M.4
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4
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b) E. M. Stocking, J. F. Sanz-Cevera, R. M. Williams, Angew. Chem. 2001, 113, 1336-1338;
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(2001)
Angew. Chem
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Stocking, E.M.1
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Williams, R.M.3
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5
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0035794943
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Angew. Chem. Int. Ed. 2001, 40, 1296-1298;
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Chem. Int. Ed
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c) E. M. Stocking, R. M. Williams, J. F. Sanz-Cevera, J. Am. Chem. Soc. 2000, 122, 4489-4493.
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J. Am. Chem. Soc
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Stocking, E.M.1
Williams, R.M.2
Sanz-Cevera, J.F.3
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7
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0041651211
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For a review on the biosynthesis of prenylated tryptophan alkaloids, see
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For a review on the biosynthesis of prenylated tryptophan alkaloids, see: R. M. Williams, E. M. Stocking, J. F. Sanz-Cevera, Top. Curr. Chem. 2000, 209, 98-173.
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Williams, R.M.1
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Sanz-Cevera, J.F.3
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8
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34250894711
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See the preceding Communication: H. Kato, T. Yoshida, T. Tokue, Y. Nojiri, H. Hirota, T. Ohta, R. M. Williams, S. Tsukamoto, Angew. Chem. 2007, 119, 2304-2306;
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See the preceding Communication: H. Kato, T. Yoshida, T. Tokue, Y. Nojiri, H. Hirota, T. Ohta, R. M. Williams, S. Tsukamoto, Angew. Chem. 2007, 119, 2304-2306;
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9
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Angew. Chem. Int. Ed. 2007, 46, 2254-2256.
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a) J. Qian-Cutrone, S. Haung, Y-Z. Shu, D. Vyas, C. Fairchild, Z. Menendez, K. Krampitz, R. Dalterio, S. E. Klohr, Q. Gao, J. Am. Chem. Soc. 2002, 124, 14 556-14 557;
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J. Am. Chem. Soc
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Qian-Cutrone, J.1
Haung, S.2
Shu, Y.-Z.3
Vyas, D.4
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Dalterio, R.8
Klohr, S.E.9
Gao, Q.10
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11
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34250797698
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US Patent 6,291,461
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b) J. Qian-Cutrone, K. D. Krampitz, Y.-Z. Shu, L. P. Chang, US Patent 6,291,461, 2001.
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Qian-Cutrone, J.1
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12
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17644361896
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For total syntheses of the stephacidins, see: a
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For total syntheses of the stephacidins, see: a) S. B. Herzon, A. G. Myers, J. Am. Chem. Soc. 2005, 127, 5342-5344;
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Baran, P.S.1
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Angew. Chem. Int. Ed. 2005, 44, 606-609;
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Chem. Int. Ed
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c) P. S. Baran, C. A. Guerrero, N. B. Ambhaikar, B. J. Hafensteiner, Angew. Chem. 2005, 117, 3960-3963;
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Angew. Chem
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Angew. Chem. Int. Ed. 2005, 44, 3892-3895;
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Chem. Int. Ed
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d) P. S. Baran, B. D. Hafensteiner, N. B. Ambhaikar, C. A. Guerrero, J. D. Gallagher, J. Am. Chem. Soc. 2006, 128, 8678-8693;
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see also the following Communication: T. J. Greshock, A. W. Grubbs, S. Tsukamoto, R. M. Williams, Angew. Chem. 2007, 119, 2312-2315;
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e) see also the following Communication: T. J. Greshock, A. W. Grubbs, S. Tsukamoto, R. M. Williams, Angew. Chem. 2007, 119, 2312-2315;
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0028566539
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For syntheses of other indole alkaloids containing a pyrrolo-indole ring system, see: a
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For syntheses of other indole alkaloids containing a pyrrolo-indole ring system, see: a) S. P. Marsden, K. M. Depew, S. J. Danishefsky, J. Am. Chem. Soc. 1994, 116, 11 143-11 144;
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34250832428
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The structures of the norgeamides were published on the internet detailing some aspects of the research performed at the Hans-Knöll Institute. See: The pdf file describing the norgeamides has been removed from the website of the Hans-Knöll Institute, but is still accessible through internet searches with the key word norgeamide
-
The structures of the norgeamides were published on the internet detailing some aspects of the research performed at the Hans-Knöll Institute. See: http://www.hki-jena.de/ The pdf file describing the norgeamides has been removed from the website of the Hans-Knöll Institute, but is still accessible through internet searches with the key word "norgeamide".
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For previous successful oxidations of the C2=C3 indole bond using meta-chloroperoxybenzoic acid or tBuOCl, see: a R. M. Williams, T. Glinka, E. Kwast, H. Coffman, J. Am. Chem. Soc. 1990, 112, 808-821;
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For previous successful oxidations of the C2=C3 indole bond using meta-chloroperoxybenzoic acid or tBuOCl, see: a) R. M. Williams, T. Glinka, E. Kwast, H. Coffman, J. Am. Chem. Soc. 1990, 112, 808-821;
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For previous reports of one-pot procedures generating oxindoles from indoles, see: a
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For previous reports of one-pot procedures generating oxindoles from indoles, see: a) N. Finch, W. I. Taylor, J. Am. Chem. Soc. 1962, 84, 1318-1320;
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