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Volumn 65, Issue 17, 2000, Pages 5436-5439

Preparation of a cis-isoprostane synthon

Author keywords

[No Author keywords available]

Indexed keywords

ICOSANOID; ISOPROSTANE DERIVATIVE;

EID: 0034714461     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000565d     Document Type: Article
Times cited : (25)

References (54)
  • 15
    • 0032563990 scopus 로고    scopus 로고
    • (h) Taber, D. F.; Kanai, K. Tetrahedron 1998, 54 11767. Pudukulathan, Z.; Manna, S.; Hwang, S.-W.; Khanapure, S. P.; Lawson, J. A.; FitzGerald, G. A.; Rokach, J. J. Am. Chem. Soc. 1998, 120, 11953.
    • (1998) Tetrahedron , vol.54 , pp. 11767
    • Taber, D.F.1    Kanai, K.2
  • 18
    • 0025942580 scopus 로고
    • For leading references to syntheses of the cis isoprostanes, see: (a) Larock, R. C.; Lee, N. H. J. Am. Chem. Soc. 1991, 113, 7815.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7815
    • Larock, R.C.1    Lee, N.H.2
  • 34
    • 0343246291 scopus 로고    scopus 로고
    • note
    • Structural optimizations were carried out using Mechanics as provided on the Oxford Scientific CAChe Workstation. CAChe uses an augmented version of Allinger's MM2 force field.
  • 44
    • 0343246288 scopus 로고    scopus 로고
    • note
    • The 1,2-diol was less than 10% of the total product. We were not able to isolate it.
  • 48
    • 0033537918 scopus 로고    scopus 로고
    • (b) A recently reported preparation of diazoacetates relies on a similar approach: Sato, H.; Kim, Y. S.; Shibasaki, M. Tetrahedron Lett. 1999, 40, 2973.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2973
    • Sato, H.1    Kim, Y.S.2    Shibasaki, M.3
  • 50
    • 0030001950 scopus 로고    scopus 로고
    • Doyle has also observed a preference for the cis diastereomer from Rh-mediated C-H insertion a to an ether: Doyle, M. P.; Kalinin, A. V. Tetrahedron Lett. 1996, 37, 1371.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1371
    • Doyle, M.P.1    Kalinin, A.V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.