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Volumn 29, Issue 48, 1988, Pages 6243-6246

The hydroalumination of ω-terbutoxy alkynes an easy access to ω-hydroxy alkenyl iodides application to the synthesis of dienic insect pheromones

Author keywords

[No Author keywords available]

Indexed keywords


EID: 17444413314     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)82315-1     Document Type: Article
Times cited : (62)

References (18)
  • 10
    • 84942713036 scopus 로고
    • Stereoselective Syntheses of (E)- and (Z)-1-Halo-1-alkenes from 1-Alkynylsilanes
    • (1981) Synthesis , pp. 999
    • On1    Lewis2    Zweifel3
  • 13
    • 84918159638 scopus 로고    scopus 로고
    • This abnormal anti hydroalumination was already observed in the propargylic series by M.J. Weiss ref. 3f
  • 15
    • 0001245736 scopus 로고
    • The corresponding E isomers, useful synthons in prostaglandin synthesis, have been prepared by hydrostanation of homopropargylic alcohols
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 222
    • Corey1    Ulrich2    Fitzpatrick3
  • 16
    • 84989456545 scopus 로고
    • Carbometallation (C-Metallation) of Alkynes: Stereospecific Synthesis of Alkenyl Derivatives
    • (1981) Synthesis , pp. 841
    • Normant1    Alexakis2
  • 18
    • 84918159637 scopus 로고    scopus 로고
    • Compound 6 is a potent pheromone component in some processionary moth species: Dr C. Descoins (Institut National de la Recherche Agronomique): personal communication.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.