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Volumn 71, Issue 17, 2006, Pages 6547-6561

General strategy for the syntheses of corynanthe, tacaman, and oxindole alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; NUCLEOPHILE; ORGANOCUPRATE; RING-CLOSING METATHESIS (RCM);

EID: 33747446952     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061032t     Document Type: Article
Times cited : (114)

References (105)
  • 10
    • 0032580376 scopus 로고    scopus 로고
    • For selected reviews of olefin metathesis, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413.
    • (1998) Tetrahedron , vol.54 , pp. 4413
    • Grubbs, R.H.1    Chang, S.2
  • 16
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, Germany
    • (g) Handbook of Metathesis; Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, Germany, 2003; Vol. 2.
    • (2003) Handbook of Metathesis , vol.2
  • 26
    • 0004784591 scopus 로고
    • Phillipson, J. D., Zenk, M. H., Eds.; Academic Press: London; Chapter 6
    • Stöckigt, J. In Indole and Biogenetically Related Alkaloids; Phillipson, J. D., Zenk, M. H., Eds.; Academic Press: London, 1980; Chapter 6, p 113.
    • (1980) Indole and Biogenetically Related Alkaloids , pp. 113
    • Stöckigt, J.1
  • 27
    • 0013848559 scopus 로고
    • The atoms are numbered according to the "biogenetic numbering" of Le Men and Taylor: Le Men, J.; Taylor, W. I. Experientia 1965, 21, 508.
    • (1965) Experientia , vol.21 , pp. 508
    • Le Men, J.1    Taylor, W.I.2
  • 28
    • 0037136473 scopus 로고    scopus 로고
    • For a preliminary account of some of these results, see: Deiters, A.; Martin, S. F. Org. Lett. 2002, 4, 3243.
    • (2002) Org. Lett. , vol.4 , pp. 3243
    • Deiters, A.1    Martin, S.F.2
  • 29
    • 0035951571 scopus 로고    scopus 로고
    • and references therein
    • For approaches to homoallylic amines, see: (a) Neipp, C. E.; Humphrey, J. M.; Martin, S. F. J. Org. Chem. 2001, 66, 531 and references therein.
    • (2001) J. Org. Chem. , vol.66 , pp. 531
    • Neipp, C.E.1    Humphrey, J.M.2    Martin, S.F.3
  • 34
    • 0035743565 scopus 로고    scopus 로고
    • Reviews on Zr- and Ti-catalyzed carbomagnesations: (a) Negishi, E.-I. Pure Appl. Chem. 2001, 73, 239.
    • (2001) Pure Appl. Chem. , vol.73 , pp. 239
    • Negishi, E.-I.1
  • 51
    • 0003540638 scopus 로고
    • Saxton, J. E., Ed.; Wiley-Interscience: New York; Supplement , Chapter 3
    • Lounasmaa, M.; Tolvanen, A. In Monoterpenoid Indole Alkaloids; Saxton, J. E., Ed.; Wiley-Interscience: New York, 1994; Supplement to Vol. 25, Part 4, Chapter 3.
    • (1994) Monoterpenoid Indole Alkaloids , vol.25 , Issue.PART 4
    • Lounasmaa, M.1    Tolvanen, A.2
  • 69
    • 33747420994 scopus 로고    scopus 로고
    • note
    • 2O with or without TMSC1 as an additive.
  • 80
    • 33747401297 scopus 로고    scopus 로고
    • note
    • For related 1,4-additions, see ref 21g and references therein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.