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Volumn 61, Issue 2, 2005, Pages 501-506

Preparation of isoxazol(in)yl substituted selenides and their further deselenenylation reaction to synthesize 3,5-disubstituted isoxazoles

Author keywords

1,3 Dipolar cycloaddition; Isoxazoles; Isoxazolines; Selenoxide syn elimination

Indexed keywords

ISOXAZOLE DERIVATIVE; ISOXAZOLINE DERIVATIVE; SELENIDE;

EID: 9744268224     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.10.071     Document Type: Article
Times cited : (20)

References (25)
  • 19
    • 33845558041 scopus 로고
    • The stereochemistry of obtained olefin is high with excellent control of Z geometry when unstable Wittig reagent was used, see: (a) E. Vedejs, G.P. Meier, and K.A.J. Snoble J. Am. Chem. Soc. 103 1981 2823 2831
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 2823-2831
    • Vedejs, E.1    Meier, G.P.2    Snoble, K.A.J.3
  • 21
    • 9744219957 scopus 로고    scopus 로고
    • note
    • 4 (11 mmol) in 10 mL dry EtOH was slowly added. After stirring at rt for 1 h, propargyl bromide (12 mmol) was added and stirred at rt for another 2 h. Extractive workup followed by dryness and evaporation. Without further purification, phenylpropargyl selenide (1.93 g) was obtained as a single product. Yield was up to 98%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.