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Volumn 39, Issue 28, 1998, Pages 4979-4982

Synthesis of the C19 through C27 segment of okadaic acid using vinylogous urethane aldol chemistry: Part III

Author keywords

[No Author keywords available]

Indexed keywords

OKADAIC ACID;

EID: 0032500142     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00973-3     Document Type: Article
Times cited : (27)

References (27)
  • 3
    • 0010516299 scopus 로고
    • Ph.D. Thesis, University of Rochester
    • 3 Dankwardt, J. W. Ph.D. Thesis, University of Rochester, 1991.
    • (1991)
    • Dankwardt, J.W.1
  • 5
    • 0030567345 scopus 로고    scopus 로고
    • For references regarding the alkylation chemistry of the vinylogous urethane lactone enolates, see: (b) Schlessinger, R. H.; Li, Y-J. J. Am. Chem. Soc. 1996, 118, 3301-3302.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3301-3302
    • Schlessinger, R.H.1    Li, Y.-J.2
  • 10
    • 0021046824 scopus 로고
    • 8 For a review on the reduction chemistry using sodium cyanoborohydride, see: Wanner, M. J.; Koomen, G. J.; Pandit, U. K. Tetrahedron 1983, 39, 3673-3681.
    • (1983) Tetrahedron , vol.39 , pp. 3673-3681
    • Wanner, M.J.1    Koomen, G.J.2    Pandit, U.K.3
  • 15
    • 0010447345 scopus 로고    scopus 로고
    • Two inseparable minor diastereomers were also produced in the coupling reaction in a combined isolated yield of 9%. The stereochemistry of these minor products was not determined
    • 12 Two inseparable minor diastereomers were also produced in the coupling reaction in a combined isolated yield of 9%. The stereochemistry of these minor products was not determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.