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Volumn 12, Issue 17, 2010, Pages 3752-3755

Total synthesis of fostriecin: Via a regio-and stereoselective polyene hydration, oxidation, and hydroboration sequence

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; FOSTRIECIN; POLYENE; PYRONE DERIVATIVE;

EID: 77956196503     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101340n     Document Type: Article
Times cited : (49)

References (63)
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    • For a synthesis/structural correction of sultriecin, see: Burke, C. P.; Haq, N.; Boger, D. L. J. Am. Chem. Soc. 2010, 132, 2157
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    • Burke, C.P.1    Haq, N.2    Boger, D.L.3
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    • For other oxidation/reduction asymmetric hydration approaches, see
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    • For an example of a stable vinyl boronate in natural product synthesis, see: Penner, M.; Rauniyar, V.; Kaspar, L. T.; Hall, D. G. J. Am. Chem. Soc. 2009, 131, 14216
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 14216
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  • 57
    • 43449127524 scopus 로고    scopus 로고
    • We found that these vinyl-boronates rival the vinyl-trifluoroborates in terms of reaction compatibility, see
    • We found that these vinyl-boronates rival the vinyl-trifluoroborates in terms of reaction compatibility, see: Molander, G. A.; Cooper, D. J. J. Org. Chem. 2008, 73, 3885
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    • note
    • The optical rotation data for our synthetic fostriecin did not match that of the natural material. This could be a result of both the different concentration and solvent. However, our optical rotation data for 5 did match that reported by Imanishi; see Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.