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Volumn 46, Issue 13, 2007, Pages 2257-2261

A concise total synthesis of the notoamides C and D

Author keywords

Biomimetic synthesis; Indoles; Natural products; Oxidation; Pinacols

Indexed keywords

BIOMIMETICS; OXIDATION; SYNTHESIS (CHEMICAL);

EID: 34249106749     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604377     Document Type: Article
Times cited : (84)

References (45)
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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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    • For a review on the biosynthesis of prenylated tryptophan alkaloids, see
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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;
    • 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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    • 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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    • see also the following Communication: T. J. Greshock, A. W. Grubbs, S. Tsukamoto, R. M. Williams, Angew. Chem. 2007, 119, 2312-2315;
    • 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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    • For syntheses of other indole alkaloids containing a pyrrolo-indole ring system, see: a
    • 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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    • 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;
    • 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
    • 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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    • Finch, N.1    Taylor, W.I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.