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Volumn 132, Issue 28, 2010, Pages 9567-9569

Erratum: Total synthesis of (±)-aplykurodinone-1: Traceless stereochemical guidance (Journal of the American Chemical Society (2010) DOI: 10.1021/ja1035495);Total synthesis of (±)-Aplykurodinone-1: Traceless stereochemical guidance

Author keywords

[No Author keywords available]

Indexed keywords

STEREOSELECTIVITY;

EID: 77954632546     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja105280j     Document Type: Erratum
Times cited : (72)

References (53)
  • 16
    • 77954634977 scopus 로고    scopus 로고
    • For a discussion of the value of pattern analysis as a supplement to strategic bond disconnection in retrosynthetic analysis, see
    • For a discussion of the value of pattern analysis as a supplement to strategic bond disconnection in retrosynthetic analysis, see
  • 28
    • 77954636901 scopus 로고    scopus 로고
    • An alternative approach to compound 12, involving a high-yielding cyclopropanation of an electron-rich olefin was also investigated. See Supporting Information for details.
    • An alternative approach to compound 12, involving a high-yielding cyclopropanation of an electron-rich olefin was also investigated. See Supporting Information for details.
  • 30
    • 0344902741 scopus 로고
    • The stereochemistry of the 5-β-epimer was confirmed by X-ray analysis of its thiocarbonyl imidazole derivative. See Supporting Information.
    • The stereochemistry of the 5-β-epimer was confirmed by X-ray analysis of its thiocarbonyl imidazole derivative. See Supporting Information. Barton, D. H. and McCombie, S. W. J. Chem. Soc., Perkin Trans. 1 1975, 1574-1585
    • (1975) J. Chem. Soc., Perkin Trans. 1 , pp. 1574-1585
    • Barton, D.H.1    McCombie, S.W.2
  • 44
    • 77954648444 scopus 로고    scopus 로고
    • 4NF was used, extensive decomposition of the starting material was observed.
    • 4NF was used, extensive decomposition of the starting material was observed.
  • 51
    • 77954634041 scopus 로고    scopus 로고
    • note
    • Proposed transition states of the homogeneous hydrogenation with Crabtree and Wilkinson catalyst are shown below. In each case, the bulky catalyst is believed to approach the double bond from its less hindered face. However, as described above, different stereochemical outcomes were observed in these two systems. For mechanistic study of these two types of hydrogenation reaction, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.