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Volumn 46, Issue 6, 2010, Pages 937-939

Selective generation of quaternary all-carbon-centres through Heck-cyclisations: Synthesis of mesembrane

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; CARBON;

EID: 75649105729     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b923175g     Document Type: Article
Times cited : (19)

References (42)
  • 2
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    • K. Fuji Chem. Rev. 1993 93 2037 2066
    • (1993) Chem. Rev. , vol.93 , pp. 2037-2066
    • Fuji, K.1
  • 9
    • 0001656364 scopus 로고    scopus 로고
    • For reviews concerning the intramolecular Heck reaction see
    • For reviews concerning the intramolecular Heck reaction see: S. E. Gibson R. Middleton Contemp. Org. Synth. 1996 3 447 471
    • (1996) Contemp. Org. Synth. , vol.3 , pp. 447-471
    • Gibson, S.E.1    Middleton, R.2
  • 25
    • 0001609968 scopus 로고
    • For an example of similar regioselectivity following the carbopalladation of a trisubstituted alkene see
    • For an example of similar regioselectivity following the carbopalladation of a trisubstituted alkene see: S. A. Godleski K. B. Gundlach R. S. Valpey Organometallics 1985 4 296 302
    • (1985) Organometallics , vol.4 , pp. 296-302
    • Godleski, S.A.1    Gundlach, K.B.2    Valpey, R.S.3
  • 26
    • 77957033352 scopus 로고
    • S. F. Martin, The Alkaloids, ed., A. Brossi, Academic Press, New York, 1987, vol. 30, pp. 251-376
    • (1987) The Alkaloids, Ed. , pp. 251-376
    • Martin, S.F.1
  • 27
    • 53449092522 scopus 로고    scopus 로고
    • A. Brossi, Academic Press, New York, for a review on mesembrine-type/ Sceletium alkaloids see
    • A. Brossi, Academic Press, New York, for a review on mesembrine-type/ Sceletium alkaloids see: N. Gericke A. M. Viljoen J. Ethnopharmacol. 2008 119 653 663
    • (2008) J. Ethnopharmacol. , vol.119 , pp. 653-663
    • Gericke, N.1    Viljoen, A.M.2
  • 28
    • 61449118878 scopus 로고    scopus 로고
    • for comprehensive coverage of Amaryllidiceae and Sceletium alkaloids see
    • for comprehensive coverage of Amaryllidiceae and Sceletium alkaloids see: Z. Yin Nat. Prod. Rep. 2009 26 363 381
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 363-381
    • Yin, Z.1
  • 39
    • 75649108292 scopus 로고    scopus 로고
    • note
    • 3 at 130 °C resulted in full conversion. However, the formation of the hydrodehalogenation product was also observed
  • 40
    • 75649116539 scopus 로고    scopus 로고
    • note
    • 2 was 0.1109 (all data). CCDC 742478
  • 41
    • 56649116045 scopus 로고    scopus 로고
    • This type of process has some precedent and has been termed a multi-task catalytic method. For a recent example see: and literature cited within
    • This type of process has some precedent and has been termed a multi-task catalytic method. For a recent example see: M. L. Kantam R. Chakravarti V. R. Chintareddy B. Sreedhar S. Bhargava Adv. Synth. Catal. 2008 350 2544 2550
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2544-2550
    • Kantam, M.L.1    Chakravarti, R.2    Chintareddy, V.R.3    Sreedhar, B.4    Bhargava, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.