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Volumn 31, Issue 41, 1990, Pages 5917-5920

A stereoselective route to trans-2,5-disubstituted tetrahydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

TETRAHYDROFURAN DERIVATIVE;

EID: 0025090654     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97993-0     Document Type: Article
Times cited : (42)

References (22)
  • 15
    • 84918642887 scopus 로고    scopus 로고
    • The detailed procedure will be published.
  • 16
    • 0001042585 scopus 로고
    • STEREOCONTROLLED IODOLACTONIZATION OF ACYCLIC OLEFINIC ACIDS: THE trans AND cis ISOMERS OF 4,5-DIHYDRO-5-IODOMETHYL-4-PHENYL-2(3H)-FURANONE
    • The absence of potassium carbonate resulted in somewhat lower yield and stereoselectivity, probably due to more thermodynamic conditions:
    • (1986) Organic Syntheses , vol.64 , pp. 175
    • Gonzalez1    Bartlett2
  • 17
    • 84918618203 scopus 로고    scopus 로고
    • The stereochemistry was assigned by NOE experiments and the ratio was determined by HPLC analysis. All new compounds showed satisfactory spectral data.
  • 21
    • 84918626920 scopus 로고    scopus 로고
    • An equivlent of Lewis acid was used. A catalytic amount of Lewis acid gave lower chemical conversion and stereoselectivity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.