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Volumn 35, Issue 45, 1994, Pages 8349-8352

Stereoselective synthesis of substituted tetrahydrofurans and butyrolactones by a new nickel catalyzed carbozincation

Author keywords

[No Author keywords available]

Indexed keywords

GAMMA BUTYROLACTONE DERIVATIVE; TETRAHYDROFURAN DERIVATIVE;

EID: 0027986915     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)74404-2     Document Type: Article
Times cited : (52)

References (29)
  • 1
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    • Boivin1
  • 3
  • 5
    • 0027376630 scopus 로고
    • Stereoselective approach to trisubstituted tetrahydrofurans
    • (1993) Tetrahedron Letters , vol.34 , pp. 6251
    • Mohr1
  • 10
    • 85034888201 scopus 로고
    • Reductive Cyclization of Ethyl 3-Allyloxy-2-bromopropionates with Chromium(II) Acetate to Tetrahydrofurans
    • A related chromium(II) mediated radical ring closure has been reported
    • (1990) Synlett , pp. 44
    • Lübbers1    Schäfer2
  • 11
    • 84988064236 scopus 로고
    • Synthetic Use of the Organochromium(III) Intermediate in the Reductive Cyclization of Δ6,7-Unsaturated α-Bromo Esters with Chromium(II) Acetate
    • (1992) Synlett , pp. 743
    • Lübbers1    Schäfer2
  • 12
    • 85064276422 scopus 로고
    • Iodo-Atom-Transfer Cyclizations of Δ6,7-Unsaturated 2-Iodo Esters with Chromium(II) Acetate
    • (1991) Synlett , pp. 861
    • Lübbers1    Schäfer2
  • 13
    • 0027276964 scopus 로고
    • New methods for reductive free-radical cyclizations of α-bromoacetals to 2-alkoxytetrahydrofurans with activated chromium(II)-acetate
    • (1993) Tetrahedron , vol.49 , pp. 4559
    • Hackmann1    Schäfer2
  • 17
    • 33748366516 scopus 로고
    • Regio-selectivity and stereo-selectivity in radical reactions
    • (1981) Tetrahedron , vol.37 , pp. 3073
    • Beckwith1
  • 18
    • 0000020896 scopus 로고
    • Regio- and stereo-selectivity of alkenyl radical ring closure: A theoretical study
    • (1985) Tetrahedron , vol.41 , pp. 3925
    • Beckwith1    Schiesser2
  • 22
    • 0025015338 scopus 로고
    • Synthesis of optically active α-trimethylsilyl δα,β-butenolides and their conversion into various butenolides and saturated γ-lactones
    • (1990) Tetrahedron Letters , pp. 6399
    • Ito1    Okamoto2    Sato3
  • 24
    • 84913010222 scopus 로고    scopus 로고
    • 4Cl solution [[Truncated]]
  • 25
    • 0008558660 scopus 로고
    • A Mild Method for the Preparation of Functionalised, Unsymmetrical Ketene Acetals
    • 2 (−30 to 0 °C, 3 h; 64% yield). The iodo-acetals 1a–e and 5b were obtained similarly (70–87% yield).
    • (1989) Synthetic Communications , vol.19 , pp. 21
    • Simpkins1    Middleton2
  • 26
    • 84912961795 scopus 로고    scopus 로고
    • The relative stereochemistry has been established with the aid of two dimensional NMR-spectroscopy.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.