메뉴 건너뛰기




Volumn 62, Issue 19, 1997, Pages 6638-6657

Total Synthesis of Halicholactone and Neohalicholactone

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000163873     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo962312j     Document Type: Article
Times cited : (61)

References (115)
  • 2
    • 0029073797 scopus 로고
    • Preliminary communications: (a) Critcher, D. J.; Connolly, S.; Wills, M. J. Chem. Soc., Chem. Commun., 1995, 139. (b) Critcher, D. J.; Connolly, S.; Wills, M. Tetrahedron Lett., 1995, 36, 3763.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 3763
    • Critcher, D.J.1    Connolly, S.2    Wills, M.3
  • 11
    • 0030459935 scopus 로고    scopus 로고
    • (c) For a recent review see Gerwick, W. H. Lipids, 1996, 31, 1215.
    • (1996) Lipids , vol.31 , pp. 1215
    • Gerwick, W.H.1
  • 78
    • 33845552981 scopus 로고
    • A methylidene carbene to acetylene rearrangement barrier of only 0.9 kcal/mol has been calculated; see (a) Stang, P. J. Acc. Chem. Res., 1982, 15, 348. (b) Stang, P. J. Chem. Rev., 1987, 78, 383. (c) Likhotvorik, I. R.; Brown, D. W.; Jones, Jr., M. J. Am. Chem. Soc., 1994, 116, 6175. (d) Ochiai, M.; Ito, T.; Takaoka, Y.; Masaki, Y.; Kunishima, M.; Tani, S.; Nagao, Y. J. Chem, Soc., Chem. Commun., 1990, 118.
    • (1982) Acc. Chem. Res. , vol.15 , pp. 348
    • Stang, P.J.1
  • 79
    • 33947094631 scopus 로고
    • A methylidene carbene to acetylene rearrangement barrier of only 0.9 kcal/mol has been calculated; see (a) Stang, P. J. Acc. Chem. Res., 1982, 15, 348. (b) Stang, P. J. Chem. Rev., 1987, 78, 383. (c) Likhotvorik, I. R.; Brown, D. W.; Jones, Jr., M. J. Am. Chem. Soc., 1994, 116, 6175. (d) Ochiai, M.; Ito, T.; Takaoka, Y.; Masaki, Y.; Kunishima, M.; Tani, S.; Nagao, Y. J. Chem, Soc., Chem. Commun., 1990, 118.
    • (1987) Chem. Rev. , vol.78 , pp. 383
    • Stang, P.J.1
  • 80
    • 0001553497 scopus 로고
    • A methylidene carbene to acetylene rearrangement barrier of only 0.9 kcal/mol has been calculated; see (a) Stang, P. J. Acc. Chem. Res., 1982, 15, 348. (b) Stang, P. J. Chem. Rev., 1987, 78, 383. (c) Likhotvorik, I. R.; Brown, D. W.; Jones, Jr., M. J. Am. Chem. Soc., 1994, 116, 6175. (d) Ochiai, M.; Ito, T.; Takaoka, Y.; Masaki, Y.; Kunishima, M.; Tani, S.; Nagao, Y. J. Chem, Soc., Chem. Commun., 1990, 118.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 6175
    • Likhotvorik, I.R.1    Brown, D.W.2    Jones Jr., M.3
  • 81
    • 37049082435 scopus 로고
    • A methylidene carbene to acetylene rearrangement barrier of only 0.9 kcal/mol has been calculated; see (a) Stang, P. J. Acc. Chem. Res., 1982, 15, 348. (b) Stang, P. J. Chem. Rev., 1987, 78, 383. (c) Likhotvorik, I. R.; Brown, D. W.; Jones, Jr., M. J. Am. Chem. Soc., 1994, 116, 6175. (d) Ochiai, M.; Ito, T.; Takaoka, Y.; Masaki, Y.; Kunishima, M.; Tani, S.; Nagao, Y. J. Chem, Soc., Chem. Commun., 1990, 118.
    • (1990) J. Chem, Soc., Chem. Commun. , pp. 118
    • Ochiai, M.1    Ito, T.2    Takaoka, Y.3    Masaki, Y.4    Kunishima, M.5    Tani, S.6    Nagao, Y.7
  • 90
    • 0001493570 scopus 로고
    • For intramolecular trapping of an alkylidenecarbene-iodonium ylide with triethylsilane, see; (a) Kitamura, T.; Stang, P. J. Tetrahedron Lett., 1988, 29, 1887. For the formation of enol ethers and enamines via the intramolecular reaction of a free alkylidene carbene with an alcohol or amine, see (b) Gilbert, J. C.; Weerasooriya, U. J. Org. Chem., 1983, 48, 448.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 1887
    • Kitamura, T.1    Stang, P.J.2
  • 91
    • 0008166853 scopus 로고
    • For intramolecular trapping of an alkylidenecarbene-iodonium ylide with triethylsilane, see; (a) Kitamura, T.; Stang, P. J. Tetrahedron Lett., 1988, 29, 1887. For the formation of enol ethers and enamines via the intramolecular reaction of a free alkylidene carbene with an alcohol or amine, see (b) Gilbert, J. C.; Weerasooriya, U. J. Org. Chem., 1983, 48, 448.
    • (1983) J. Org. Chem. , vol.48 , pp. 448
    • Gilbert, J.C.1    Weerasooriya, U.2
  • 102
    • 0000610844 scopus 로고
    • (c) Kishi, Y. Pure Appl. Chem., 1992, 64, 343. During the course of our work Kishi published in detail on his attempts to design an efficient chiral ligand for the Ni(II)/Cr(II) coupling reaction. To date the best ligand is based on a 2,2′-dipyridyl ring system, which has only produced modest levels of diastereoselection in chosen coupling reactions,
    • (1992) Pure Appl. Chem. , vol.64 , pp. 343
    • Kishi, Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.