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Volumn 75, Issue 21, 2010, Pages 7461-7464

Stereoselective α,α′-annelation reactions of 1,3-dioxan-5-ones

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANE RING; CYCLOHEXANONES; DIOXANE RINGS; ENAMINES; EPIMERIZATION; ESTER GROUPS; PYRROLIDINES; RING SYSTEMS; STEREO-SELECTIVE; STEREOCONTROL; STEREOELECTRONIC INTERACTIONS;

EID: 78049495224     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101531b     Document Type: Article
Times cited : (13)

References (43)
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    • Smith, A.B.1    Empfield, J.R.2
  • 5
    • 29744451180 scopus 로고    scopus 로고
    • For reviews on diastereotopic group selective reactions see
    • For reviews on diastereotopic group selective reactions see: Studer, A.; Schleth, F. Synlett 2005, 3033
    • (2005) Synlett , pp. 3033
    • Studer, A.1    Schleth, F.2
  • 36
    • 33750064473 scopus 로고    scopus 로고
    • For a review on the synthetic utility of dihydroxyacetone derivatives see
    • For a review on the synthetic utility of dihydroxyacetone derivatives see: Enders, D.; Voith, M.; Lenzen, A. Angew. Chem., Int. Ed. 2005, 44, 2
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 2
    • Enders, D.1    Voith, M.2    Lenzen, A.3
  • 38
    • 78049519433 scopus 로고    scopus 로고
    • A file in CIF format is available in the Supporting Information. CCDC 779722 - 779726 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • A file in CIF format is available in the Supporting Information. CCDC 779722-779726 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/datarequest/cif.
  • 39
    • 84990465786 scopus 로고
    • For a review on conformational analysis of bicyclo[3.3.1]nonanes and their heteroanalogues see
    • For a review on conformational analysis of bicyclo[3.3.1]nonanes and their heteroanalogues see: Zefirov, N. S.; Palyulin, V. A. Top. Stereochem. 1991, 20, 171
    • (1991) Top. Stereochem. , vol.20 , pp. 171
    • Zefirov, N.S.1    Palyulin, V.A.2
  • 41
    • 78049522292 scopus 로고    scopus 로고
    • Peters has proposed that α,α′-annelation reactions can proceed through an alternative half-chair transition state (ref 8d). Application of this model to 9b, c and 10b, c fails to predict the observed isomer
    • Peters has proposed that α,α′-annelation reactions can proceed through an alternative half-chair transition state (ref 8d). Application of this model to 9b, c and 10b, c fails to predict the observed isomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.