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Volumn 28, Issue 13, 1987, Pages 1443-1446

Stereoselective synthesis of (E)-alkenylsilanes from aldehydes with a reagent prepared by chromium(II) reduction of Me3SiCHBr2

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EID: 0007850846     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)95949-5     Document Type: Article
Times cited : (77)

References (28)
  • 10
    • 0002371298 scopus 로고
    • A Convenient Route to (E)-1-Alkenylsilanes via Isomerization of (Z)-1-Alkenylsilanes
    • (1980) Synthesis , pp. 803
    • Zweifel1    On2
  • 14
    • 84862475385 scopus 로고
    • Erzeugung von und Olefinierung mit α-S-, -Se-, -Si- und -Sn-perheterosubstituierten (Trimethylsilyl)methyllithium-Verbindungen
    • (1977) Chemische Berichte , vol.110 , pp. 852
    • Groebel1    Seebach2
  • 17
    • 84918446104 scopus 로고    scopus 로고
    • T. Okazoe, K. Takai, and K. Utimoto, J. Am. Chem. Soc., in press.
  • 22
    • 0001856098 scopus 로고
    • An efficient synthesis of homoallyl alcohols by the reaction of allyl halides with carbonyl compounds in the presence of metallic tin.
    • (1981) Chemistry Letters , pp. 1527
    • Mukaiyama1    Harada2
  • 23
    • 84912431994 scopus 로고
    • An efficient method for the preparation of homoallylic alcohol derivatives by the reaction of allyl iodide with carbonyl compounds in the presence of stannous halide.
    • (1980) Chemistry Letters , pp. 1507
    • Mukaiyama1    Harada2    Shoda3
  • 27
    • 84918446103 scopus 로고    scopus 로고
    • 2 (0.98 g, 8.0 mmol) in THF (20 mL). In the case of nonanal, a THF solution of LiI (1.0 M, 4.0 mmol) is added to the mixture successively (ref. 13). After stirring at 25°C for the number of hours shown in scheme 3, the mixture is subjected to an aqueousworkup. Purification of the crude product by preparative TLC onsilica gel affords the desired vinyl sulfide.
  • 28
    • 84918446102 scopus 로고    scopus 로고
    • 30OSi: C, 70.79; H, 11.88%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.