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Volumn , Issue 11, 2011, Pages 2101-2110

A general, diastereoselective synthesis of highly functionalized bicyclo[n.3.1]alkane systems based on an anionic domino reaction of α-nitrocycloalkanones

Author keywords

Aldol reactions; Bicyclic compounds; Diastereoselectivity; Domino reactions; Michael addition

Indexed keywords


EID: 79953234822     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001672     Document Type: Article
Times cited : (16)

References (79)
  • 1
    • 33749844000 scopus 로고    scopus 로고
    • For a review of the chemistry of polycyclic polyprenylated acylphloroglucinols, including hyperforin, see.
    • For a review of the chemistry of polycyclic polyprenylated acylphloroglucinols, including hyperforin, see:, R. Ciochina, R. B. Grossman, Chem. Rev. 2006, 106, 3963-3986.
    • (2006) Chem. Rev. , vol.106 , pp. 3963-3986
    • Ciochina, R.1    Grossman, R.B.2
  • 2
    • 76249122299 scopus 로고    scopus 로고
    • The total synthesis of hyperforin has not been achieved. For the synthesis of its enantiomer, see.
    • The total synthesis of hyperforin has not been achieved. For the synthesis of its enantiomer, see:, Y. Shimizu, S.-L. Shi, H. Usuda, M. Kanai, M. Shibasaki, Angew. Chem. Int. Ed. 2010, 49, 1103-1106.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1103-1106
    • Shimizu, Y.1    Shi, S.-L.2    Usuda, H.3    Kanai, M.4    Shibasaki, M.5
  • 5
    • 79953239711 scopus 로고    scopus 로고
    • For the isolation of the welwitindolinones, see
    • For the isolation of the welwitindolinones, see
  • 8
    • 79953241094 scopus 로고    scopus 로고
    • For reviews of the chemistry of the welwitindolinones, see
    • For reviews of the chemistry of the welwitindolinones, see
  • 12
    • 79953236400 scopus 로고    scopus 로고
    • For overviews of taxol and taxanes as anticancer agents, see
    • For overviews of taxol and taxanes as anticancer agents, see
  • 16
    • 79953234333 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 18
    • 0035207263 scopus 로고    scopus 로고
    • for selected more recent work, see
    • E. Butkus, Synlett 2001, 1827-1834, for selected more recent work, see
    • (2001) Synlett , pp. 1827-1834
    • Butkus, E.1
  • 25
    • 79953245206 scopus 로고    scopus 로고
    • [12]
    • [12]
  • 26
    • 11844260494 scopus 로고    scopus 로고
    • For a review, see:, for selected more recent work, see
    • For a review, see:, C. Avendaño, J. C. Menéndez, Curr. Org. Synth. 2004, 1, 65-82, for selected more recent work, see
    • (2004) Curr. Org. Synth. , vol.1 , pp. 65-82
    • Avendaño, C.1    Menéndez, J.C.2
  • 29
    • 79953241762 scopus 로고    scopus 로고
    • [6]
    • [6]
  • 30
    • 0036048410 scopus 로고    scopus 로고
    • For a review, in the context of taxol synthesis, see: D. G. I. Kingston, for selected more recent work, see
    • For a review, in the context of taxol synthesis, see: D. G. I. Kingston, P. G. Jagtap, H. Yuan, L. Samala, Prog. Chem. Org. Nat. Prod. 2002, 84, 53-225, for selected more recent work, see
    • (2002) Prog. Chem. Org. Nat. Prod. , vol.84 , pp. 53-225
    • Jagtap, P.G.1    Yuan, H.2    Samala, L.3
  • 34
    • 79953254597 scopus 로고    scopus 로고
    • For representative examples, see
    • For representative examples, see
  • 36
    • 79953233577 scopus 로고    scopus 로고
    • [18]
    • [18]
  • 38
    • 79953240301 scopus 로고    scopus 로고
    • For reviews of diversity-oriented synthesis, see
    • For reviews of diversity-oriented synthesis, see
  • 39
  • 46
    • 79953237981 scopus 로고    scopus 로고
    • For selected reviews, see
    • For selected reviews, see
  • 55
    • 34250021382 scopus 로고    scopus 로고
    • for a monograph, see
    • A. Padwa, S. K. Bur, Tetrahedron 2007, 63, 5341-5378, for a monograph, see
    • (2007) Tetrahedron , vol.63 , pp. 5341-5378
    • Padwa, A.1    Bur, S.K.2
  • 57
    • 79953249695 scopus 로고    scopus 로고
    • For reviews of the synthetic applications of α-nitro ketones, see
    • For reviews of the synthetic applications of α-nitro ketones, see
  • 61
    • 0003527998 scopus 로고    scopus 로고
    • for a monograph on the synthetic applications of nitro compounds, see:, Wiley-VCH, Weinheim.
    • for a monograph on the synthetic applications of nitro compounds, see:, N. Ono, The Nitro Group in Organic Synthesis, Wiley-VCH, Weinheim, 2001.
    • (2001) The Nitro Group in Organic Synthesis
    • Ono, N.1
  • 64
    • 53849093470 scopus 로고    scopus 로고
    • For recent synthetic transformations subsequent to the generation of these bicyclic compounds, see.
    • For recent synthetic transformations subsequent to the generation of these bicyclic compounds, see:, Y. Coquerel, M.-H. Filippini, D. Bensa, J. Rodriguez, Chem. Eur. J. 2008, 14, 3078-3092.
    • (2008) Chem. Eur. J. , vol.14 , pp. 3078-3092
    • Coquerel, Y.1    Filippini, M.-H.2    Bensa, D.3    Rodriguez, J.4
  • 77
    • 79953235588 scopus 로고    scopus 로고
    • 3-promoted reaction, thereby displacing the equilibria in a normally unobserved direction.
    • 3-promoted reaction, thereby displacing the equilibria in a normally unobserved direction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.