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Volumn 80, Issue 5, 2008, Pages 1141-1148

Toward the total synthesis of ritterazine N

Author keywords

Chromatographic resolution; Computational organometallic chemistry; Ketone alkylation; Natural product synthesis; Spiroketal construction

Indexed keywords


EID: 44649201046     PISSN: 00334545     EISSN: None     Source Type: Journal    
DOI: 10.1351/pac200880051141     Document Type: Conference Paper
Times cited : (1)

References (23)
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    • 25444498936 scopus 로고    scopus 로고
    • For leading references, see: a
    • For leading references, see: (a) J. S. Lee, P. L. Fuchs J. Am. Chem. Soc. 127, 13122 (2005);
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 13122
    • Lee, J.S.1    Fuchs, P.L.2
  • 4
    • 33645524524 scopus 로고    scopus 로고
    • For our published work toward the ritterazines, see: a
    • For our published work toward the ritterazines, see: (a) D. F. Taber, K. V. Taluskie. J. Org. Chem. 71, 2797 (2006);
    • (2006) J. Org. Chem , vol.71 , pp. 2797
    • Taber, D.F.1    Taluskie, K.V.2
  • 6
    • 0001089453 scopus 로고    scopus 로고
    • For leading references to PM3, see: J. I. Seeman, J. B. Paine III, H. V. Secor, H. S. Im, E. R. Bernstein. J. Am. Chem. Soc. 114, 5269 (1992).
    • For leading references to PM3, see: J. I. Seeman, J. B. Paine III, H. V. Secor, H. S. Im, E. R. Bernstein. J. Am. Chem. Soc. 114, 5269 (1992).
  • 12
    • 34249094574 scopus 로고    scopus 로고
    • In parallel with our work, Shair reached the same conclusion about the relative configuration of the spiro center of the ritterazines: S. T. Phillips, M. D. Shair. J. Am. Chem. Soc. 129, 6589 (2007).
    • In parallel with our work, Shair reached the same conclusion about the relative configuration of the spiro center of the ritterazines: S. T. Phillips, M. D. Shair. J. Am. Chem. Soc. 129, 6589 (2007).
  • 13
    • 33845184216 scopus 로고    scopus 로고
    • For the development of intramolecular diene cyclozirconation, including computational analysis, see: (a) W. A Nugent, D. F Taber. J. Am. Chem. Soc. 111, 6435 (1989);
    • For the development of intramolecular diene cyclozirconation, including computational analysis, see: (a) W. A Nugent, D. F Taber. J. Am. Chem. Soc. 111, 6435 (1989);
  • 15
    • 0000284194 scopus 로고
    • For the development of Zr-based intramolecular diene cyclocarbonylation, see: a
    • For the development of Zr-based intramolecular diene cyclocarbonylation, see: (a) E. Negishi, S. R. Miller. J. Org. Chem. 54, 6014 (1989);
    • (1989) J. Org. Chem , vol.54 , pp. 6014
    • Negishi, E.1    Miller, S.R.2
  • 18
    • 33751500572 scopus 로고
    • Both ZINDO and MOPAC were used as implemented on a Tektronix CAChe workstation. For a leading reference to the use of ZINDO for transition-metal calculations, see
    • For a leading reference to the use of ZINDO for transition-metal calculations, see: D. R. Kanis, M. A. Ratner, T. J. Marks, M. C. Zerner. Chem. Mater. 3, 19 (1991). Both ZINDO and MOPAC were used as implemented on a Tektronix CAChe workstation.
    • (1991) Chem. Mater , vol.3 , pp. 19
    • Kanis, D.R.1    Ratner, M.A.2    Marks, T.J.3    Zerner, M.C.4
  • 22
  • 23
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    • For the advantages of KH in paraffin, see
    • For the advantages of KH in paraffin, see: D. F. Taber, C. G. Nelson. J. Org. Chem. 71, 8973 (2006).
    • (2006) J. Org. Chem , vol.71 , pp. 8973
    • Taber, D.F.1    Nelson, C.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.