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Tetrahedron Letters
Volumn 25, Issue 46, 1984, Pages 5231-5234
Stereocontrol in the formation of 2,3,4-trisubstituted tetrahydrofurans
Author keywords

[No Author keywords available]
Indexed keywords

EID: 0000947803     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)81571-9     Document Type: Article
Times cited : (30)
References (14)
  • 7
    • 84918414148 scopus 로고    scopus 로고
    • All yields are reported for purified samples, characterized by infrared, nuclear magnetic resonance (360 mhz) and mass spectral data. Complete details will be provided in a full account of this work.
  • 8
    • 33845557675 scopus 로고
    • The literature conditions were employed yielding epoxides 2c (90%), 2d (82%), 2e (92%) and 2ab (50% in a 1.5:1.0 ratio). We have noted that buffered MCPBA gave a similar ratio of 2ab in-85% yield.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 7690
    • Mihelich1    Daniels2    Eickhoff3
  • 10
    • 0000592263 scopus 로고
    • A study of hydroxyl participation in acyclic epoxide systems. Acid-catalysed rearrangements oftrans- andcis-3,4-Epoxypentan-1-ols, 4,5-Epoxyhexan-1-ols, and 5,6-Epoxyheptan-1-ols
    • For a detailed study:
    • (1973) Australian Journal of Chemistry , vol.26 , pp. 2521
    • Coxon1    Hartshorn2    Swallow3
  • 11
    • 84918414147 scopus 로고    scopus 로고
    • These substrates continued to produce tetrahydrofurans 3 with concomittant debenzylation, albeit in low yields.
  • 12
    • 84918414146 scopus 로고    scopus 로고
    • 1) substitution.
  • 13
    • 84918414145 scopus 로고    scopus 로고
    • Diol 3f was also converted into ether 4, and the iodide 3c cyclized readily to provide the corresponding methyl derivative of 4.
  • 14
    • 84918414144 scopus 로고    scopus 로고
    • Complete X-ray crystallographic data are available from the Indiana University Chemistry Library. Request Molecular Structure Center Report 83063.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.