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Volumn 16, Issue 50, 1975, Pages 4487-4490

Improved procedure for the generation of allyl cations from simple dibromo ketones. Change of mechanism on reaction with triethyl borate amd zinc. Cycloadditions to conjugated dienes.

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000884321     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)91100-6     Document Type: Article
Times cited : (46)

References (15)
  • 8
    • 33947294543 scopus 로고
    • Reformatsky reaction at room temperature and in the presence of trimethylborate. Improved procedures for the preparation of .beta.-hydroxy esters
    • have described Reformatsky reactions under similar experimental conditions. If our mechanistic proposal applies to their reactions, one should expect α-bromo-β-hydroxyesters to be formed at least initially.
    • (1970) The Journal of Organic Chemistry , vol.35 , pp. 3966
    • Rathke1    Lindert2
  • 13
    • 84917767150 scopus 로고
    • A CONVENIENT SYNTHESIS OF α-BROMOKETONES FROM VINYLOXYBORANES OBTAINED BY THE REACTION OF ORGANOBORANES WITH α, β-UNSATURATED KETONES
    • (1973) Chemistry Letters , pp. 1145
    • Miyaura1    Harada2    Itoh3    Suzuki4
  • 15
    • 84918010588 scopus 로고    scopus 로고
    • Work supported by the Science Research Council, the Petroleum Research Fund, administered by the American Chemical Society and a NATO Grant.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.