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Volumn 31, Issue 40, 1990, Pages 5775-5778

Reactions of triazolinedione with alkenes. A remarkable geminal selectivity.

Author keywords

[No Author keywords available]

Indexed keywords

1,2,4 TRIAZOLE DERIVATIVE;

EID: 0025002480     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97956-5     Document Type: Article
Times cited : (22)

References (18)
  • 11
    • 2642642926 scopus 로고
    • Alkenes were prepared by the following methods: dehydration of the corresponding Grignard carbinols gave alkenes 1 – 5, 8 and 12. McMurry's coupling of the proper ketones, gave olefins 6 and 7; compound 9 was synthesized by the coupling of chlorotrimethylsilane and the corresponding vinylorganolithium intermediate; compound 10 was prepared by chlorosulfenylation-dehydrochlorination of 2-methyl-2-butene, P. B. Hopkins and P. L. Fuchs J. Org. Chem. 43, 1208 (1978); and trans-13 by complete reduction of the corresponding trans ester, Y. Shen, Y Xin, and J. Zhao J. Tetrahedron Lett. 6119 (1988). Alkene isomers, where appropriate, were purified by preparative GC.
    • (1978) J. Org. Chem. , vol.43 , pp. 3255
    • McMurry1    Fleming2    Kees3    Krepski4
  • 15
    • 0002755327 scopus 로고
    • Regioselective Synthesis of 2-Hydroperoxy-2-methylenebutanoic Acid Derivatives via Photooxygenation of Tiglic Acid Derivatives
    • (1986) Synthesis , pp. 1050
    • Adam1    Griesbeck2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.