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Volumn 111, Issue 17, 1989, Pages 6648-6656

Total Synthesis of (+)-Hydroxyjatrophone a and (+)-Hydroxyjatrophone B

Author keywords

[No Author keywords available]

Indexed keywords

2ALPHA HYDROXYJATROPHONE; 2BETA HYDROXYJATROPHONE; UNCLASSIFIED DRUG;

EID: 0024390379     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00199a026     Document Type: Article
Times cited : (52)

References (13)
  • 1
    • 0021041609 scopus 로고
    • For previous studies of Jatropha gossypiifolia see: (a) Kupchan, S. M.; Sigel, C. W.; Matz, M. J.; Saenz Renauld, J. A.; Haltiwanger, R. C.; Bryan, R. F. J. Am. Chem. Soc. 1970, 92, 4476. (b) Kupchan, S. M.; Sigel, C. W.; Matz, M. J.; Gilmore, C. J.; Bryan, R. F. J. Am. Chem. Soc. 1976, 98, 2295.
    • Taylor, M. D.; Smith, III, A. B.; Furst, G. T.; Gunasekara, S. R.; Bevelle, C. A.; Cordell, G. A.; Kupchan, S. M.; Uchida, H.; Branfman, A. R.; Dailey, Jr., R. G.; Sneden, A. T. J. Am. Chem. Soc. 1983, 105, 3177. For previous studies of Jatropha gossypiifolia see: (a) Kupchan, S. M.; Sigel, C. W.; Matz, M. J.; Saenz Renauld, J. A.; Haltiwanger, R. C.; Bryan, R. F. J. Am. Chem. Soc. 1970, 92, 4476. (b) Kupchan, S. M.; Sigel, C. W.; Matz, M. J.; Gilmore, C. J.; Bryan, R. F. J. Am. Chem. Soc. 1976, 98, 2295.
    • (1983) J. Am. Chem. Soc. , vol.105 , Issue.3177
    • Taylor, M.D.1    Smith, A.B.2    Furst, G.T.3    Gunasekara, S.R.4    Bevelle, C.A.5    Cordell, G.A.6    Kupchan, S.M.7    Uchida, H.8    Branfman, A.R.9    Dailey, R.G.10    Sneden, A.T.11
  • 3
    • 85012713120 scopus 로고
    • Lindberg, T., Ed.; Academic: Orlando, FL (b) Smith, III, A. B.; Guaciaro, M. A.; Schow, S. R.; Wovkulich, P. M.; Toder, B. H.; Hall, T. W. J. Am. Chem. Soc. 1981, 103, 219. See also: Smith, III, A. B.; Guaciaro, M. A.; Schow, S. R.; Wovkulich, P. M.; Toder, B. H.; Hall, T. W. J. Am. Chem. Soc. 1981, 103, 4652. Taylor, M. D.; Smith, III, A. B.; Malamas, M. S. J. Org. Chem. 1983, 48, 4257
    • (a) Smith, II I.A.B. Strategies and Tactics in Organic Synthesis; Lindberg, T., Ed.; Academic: Orlando, FL, 1984; Vol. 1, p 223, (b) Smith, III, A. B.; Guaciaro, M. A.; Schow, S. R.; Wovkulich, P. M.; Toder, B. H.; Hall, T. W. J. Am. Chem. Soc. 1981, 103, 219. See also: Smith, III, A. B.; Guaciaro, M. A.; Schow, S. R.; Wovkulich, P. M.; Toder, B. H.; Hall, T. W. J. Am. Chem. Soc. 1981, 103, 4652. Taylor, M. D.; Smith, III, A. B.; Malamas, M. S. J. Org. Chem. 1983, 48, 4257.
    • (1984) Strategies and Tactics in Organic Synthesis , vol.1 , pp. 223
    • Smith, I.A.B.1
  • 4
    • 0000011222 scopus 로고
    • (b) Smith, III, A. B.; Liverton, N. J.; Hrib, N. J.; Sivaramakrishnan, H.; Winzenberg, K. J. Am. Chem. Soc. 1986, 108, 3040.
    • (a) Smith, II I.A.B.; Liverton, N. J.; Hrib, N. J.; Sivaramakrishnan, H.; Winzenberg, K. J. Org. Chem. 1985, 50, 3239. (b) Smith, III, A. B.; Liverton, N. J.; Hrib, N. J.; Sivaramakrishnan, H.; Winzenberg, K. J. Am. Chem. Soc. 1986, 108, 3040.
    • (1985) J. Org. Chem. , vol.50 , pp. 3239
    • Smith, I.A.1    Liverton, N.J.2    Hrib, N.J.3    Sivaramakrishnan, H.4    Winzenberg, K.5
  • 5
    • 0002084085 scopus 로고
    • (b) Banno, K.; Mukaiyama, T. Chem. Lett. 1975, 741. (c) Mukaiyama, T.; Ishida, A. Chem. Lett. 1975, 305.
    • (a) Mukaiyama, T.; Yayashi, M. Chem. Lett. 1974, 15. (b) Banno, K.; Mukaiyama, T. Chem. Lett. 1975, 741. (c) Mukaiyama, T.; Ishida, A. Chem. Lett. 1975, 305.
    • (1974) Chem. Lett. , pp. 15
    • Mukaiyama, T.1    Yayashi, M.2
  • 7
    • 2142755753 scopus 로고
    • For the preparation of 12 from the corresponding acid see For (S)-(+)-O-methylmandelic acid see: Bonner, W. A. J. Am. Chem. Soc. 1951, 73, 3126.
    • For the preparation of 12 from the corresponding acid see: Jennison, C. P. R.; Mackay, D. Tetrahedron 1973, 29, 1255. For (S)-(+)-O-methylmandelic acid see: Bonner, W. A. J. Am. Chem. Soc. 1951, 73, 3126.
    • (1973) Tetrahedron , vol.29 , pp. 1255
    • Jennison, C.P.R.1    Mackay, D.2
  • 8
    • 0042366946 scopus 로고
    • For the preparation of aluminum hydride from lithium aluminum hydride and 100% sulfuric acid see: (a) (b) Brown, H. C.; Yoon, N. M. J. Am. Chem. Soc. 1966, 88, 1464.
    • For the preparation of aluminum hydride from lithium aluminum hydride and 100% sulfuric acid see: (a) Ashby, E. C.; Sanders, J. R.; Claudy, P.; Schwartz, R. J. Am. Chem. Soc. 1973, 95, 6485. (b) Brown, H. C.; Yoon, N. M. J. Am. Chem. Soc. 1966, 88, 1464.
    • (1973) J. Am. Chem. Soc. , vol.95 , Issue.6485
    • Ashby, E.C.1    Sanders, J.R.2    Claudy, P.3    Schwartz, R.4
  • 11
    • 0003514816 scopus 로고
    • Reagents for Organic Synthesis
    • Wiley: New York See also: Hutchins, R. O.; Hutchins, M. G. K. The Chemistry of Triple-bonded Functional Groups, Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, 1983; Suppl. C, Part 1; p 571, and references therein.
    • Fieser, L.; Fieser, M. Reagents for Organic Synthesis, Wiley: New York, 1967; Vol. 1, p 566. See also: Hutchins, R. O.; Hutchins, M. G. K. The Chemistry of Triple-bonded Functional Groups, Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, 1983; Suppl. C, Part 1; p 571, and references therein.
    • (1967) , vol.1 , pp. 566
    • Fieser, L.1    Fieser, M.2


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