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Volumn 25, Issue 25, 1984, Pages 2691-2694

Palladium(II)-catalyzed epoxidation of olefins with α-silyloxyalkyl peroxybenzoates

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Indexed keywords


EID: 0000048511     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)81264-8     Document Type: Article
Times cited : (18)

References (16)
  • 1
    • 84914407633 scopus 로고    scopus 로고
    • I. Saito, R. Nagata and T. Matsuura, Tetrahedron Lett., preceding paper in this issue.
  • 2
    • 84914407632 scopus 로고    scopus 로고
    • Epoxidation of olefins has been observed with 1b and 1c. However, production of a Baeyer-Villiger product is inevitable in the case of 1b. The use of 1c requires longer time and higher temperature.
  • 3
    • 84914407631 scopus 로고    scopus 로고
    • 2 were found to be equally effective.
  • 5
    • 84914407630 scopus 로고    scopus 로고
    • 2 (22 mg, 0.1 mmol) at room temperature. The mixture was stirred for 5 h under nitrogen. After evaporation the residue was chromatographed on silica gel to give β,β-dimethylstyrene oxide (130 mg, 88%).
  • 9
    • 0003092156 scopus 로고
    • A new preparative method for 1,3-dicarbonyl compounds by the regioselective oxidation of .ALPHA.,.BETA.-unsaturated carbonyl compounds, catalyzed by PdCl2 using hydroperoxides as the reoxidant of Pd0.
    • (1980) Chemistry Letters , pp. 257
    • Tsuji1    Nagashima2    Hori3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.