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Volumn 39, Issue 51, 1998, Pages 9361-9364

A divergent approach to the myriaporones and tedanolide: Enantioselective preparation of the common intermediate

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; ALLYL COMPOUND; MACROLIDE; MYRIAPORONE; NATURAL PRODUCT; PROPIONIC ACID DERIVATIVE; TEDANOLIDE; UNCLASSIFIED DRUG; ZIRCONIUM;

EID: 0032542158     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02110-8     Document Type: Article
Times cited : (54)

References (20)
  • 1
    • 85038544400 scopus 로고    scopus 로고
    • June 22-26, Trinity University San Antonio, TX; abstract No. M71
    • 1. Presented at the 35th National Organic Chemistry Symposium, June 22-26, 1997, Trinity University San Antonio, TX; abstract No. M71.
    • (1997) 35th National Organic Chemistry Symposium
  • 11
    • 0010324359 scopus 로고
    • 7. Caserio, F. F.; Dennis, G. E.; DeWolfe, R. H.; Young, W.G J. Am . Chem. Soc. 1955, 77, 4182-4183. From a mechanistic perspective, this reaction has been restudied on numerous occasions. However, to the best of our knowledge only Johnson has exploited the stereoselectivity of this interesting reaction from a synthetic perspective; Johnson, W. S.; Li, T.-T.; Harbert, C. A.; Bartlett, W. R.; Herrin, T. R.; Staskun, B.; Rich, D. H. J. Am. Chem. Soc. 1970, 92, 4461-4463.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 4182-4183
    • Caserio, F.F.1    Dennis, G.E.2    DeWolfe, R.H.3    Young, W.G.4
  • 12
    • 0014948729 scopus 로고
    • 7. Caserio, F. F.; Dennis, G. E.; DeWolfe, R. H.; Young, W.G J. Am . Chem. Soc. 1955, 77, 4182-4183. From a mechanistic perspective, this reaction has been restudied on numerous occasions. However, to the best of our knowledge only Johnson has exploited the stereoselectivity of this interesting reaction from a synthetic perspective; Johnson, W. S.; Li, T.-T.; Harbert, C. A.; Bartlett, W. R.; Herrin, T. R.; Staskun, B.; Rich, D. H. J. Am. Chem. Soc. 1970, 92, 4461-4463.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 4461-4463
    • Johnson, W.S.1    Li, T.-T.2    Harbert, C.A.3    Bartlett, W.R.4    Herrin, T.R.5    Staskun, B.6    Rich, D.H.7
  • 19
    • 85038550103 scopus 로고    scopus 로고
    • University of Notre Dame, unpublished results
    • 14. Hearn, B. R.; University of Notre Dame, unpublished results.
    • Hearn, B.R.1
  • 20
    • 85038544091 scopus 로고    scopus 로고
    • Satisfactory spectral and HRMS data has been obtained on all new compounds
    • 15. Satisfactory spectral and HRMS data has been obtained on all new compounds.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.