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Volumn 74, Issue 21, 2009, Pages 8359-8368

Total synthesis of the bridged indole alkaloid apparicine

Author keywords

[No Author keywords available]

Indexed keywords

2-INDOLYLACYL RADICALS; ALKYLIDENES; ALTERNATIVE APPROACH; CHEMICAL EQUATIONS; HECK REACTIONS; INDOLE ALKALOIDS; RING CLOSING METATHESIS; TEMPLATED; TOTAL SYNTHESIS; VINYL HALIDES;

EID: 70350728451     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901986v     Document Type: Article
Times cited : (63)

References (64)
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    • The E configuration of the ethylidene group was established some years later
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  • 9
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    • For a review, see: Cordell, G. A., Ed.; Academic Press: New York, Chapter 4
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    • Phillipson, J. D., Zenk, M. H., Eds; Academic Press: London, Chapter 8
    • Potier, P. In Indole and Biogenetically Related Alkaloids; Phillipson, J. D., Zenk, M. H., Eds; Academic Press: London, 1980; Chapter 8.
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    • Potier, P.1
  • 17
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    • General reviews: (a) de Meijere, A.; Diederich, F., Eds; Wiley-WCH: New York
    • General reviews: (a) Bráse, S.; de Meijere, A. In Metal-Catalyzed Cross-Coupling Reactions; de Meijere, A.; Diederich, F., Eds; Wiley-WCH: New York, 2004; pp 217-316.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions , pp. 217-316
    • Bráse, S.1    De Meijere, A.2
  • 30
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    • For related Heck processes involving more robust aryl halides, see: (a)
    • For related Heck processes involving more robust aryl halides, see: (a) Grigg, R.; Sridharan, V.; York, M. Tetrahedron Lett. 1998, 39, 4139-4142.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4139-4142
    • Grigg, R.1    Sridharan, V.2    York, M.3
  • 33
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    • General reviews: (a) Grubbs, R. H. Ed.; Wiley-VCH: Weinheim
    • General reviews: (a) Grubbs, R. H. Ed.; Handbook of Metathesis; Wiley-VCH: Weinheim, 2003; Vol.2.
    • (2003) Handbook of Metathesis , vol.2
  • 35
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    • For reviews, see: (a)
    • For reviews, see: (a) Maier, M. E. Angew. Chem., Int. Ed. 2000, 39, 2073-2077.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 2073-2077
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    • (b) Yet, L. Chem. Rev. 2000, 100, 2963-3007.
    • (2000) Chem. Rev. , vol.100 , pp. 2963-3007
    • Yet, L.1
  • 41
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    • Gribble, G. W., Joule, J. A., Eds; Elsevier: Amsterdam, Chapter 1
    • Bennasar, M.-L.; Roca, T. In Progress in Heterocyclic Chemistry; Gribble, G. W., Joule, J. A., Eds; Elsevier: Amsterdam, 2009; Chapter 1, pp 1-19.
    • (2009) Progress in Heterocyclic Chemistry , pp. 1-19
    • Bennasar, M.-L.1    Roca, T.2
  • 43
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    • See also ref 13b
    • (b) See also ref 13b.
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    • (b) Jeffery, T. Tetrahedron 1996, 52, 10113-10130.
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    • Jeffery, T.1
  • 49
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    • The configuration of the ethylidene substituent was established by NOESY experiments
    • The configuration of the ethylidene substituent was established by NOESY experiments.
  • 55
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    • For a recent example, see: (c)
    • For a recent example, see: (c) Schmidt, B.; Biernat, A. Chem.;Eur. J. 2008, 14, 6135-6141.
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    • Schmidt, B.1    Biernat, A.2
  • 56
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    • For reviews on the nonmetathetic behavior of Grubbs ruthenium catalysts, see: (a)
    • For reviews on the nonmetathetic behavior of Grubbs ruthenium catalysts, see: (a) Schmidt, B. Eur. J. Org. Chem. 2004, 1865-1880.
    • (2004) Eur. J. Org. Chem. , pp. 1865-1880
    • Schmidt, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.