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Volumn 50, Issue 29, 2009, Pages 4233-4235

The synthesis of 1,1′-disubstituted bis-cyclopropanes by the reaction of substituted propargylic alcohols with CH2I2-R3Al

Author keywords

[No Author keywords available]

Indexed keywords

1 ETHYNYLCYCLOHEXANOL; 1 HEXYN 3 OL; 2 PROPYN 1 YL ACETATE; 2 PROPYN 1 YL PROPIONATE; 3 METHYL 1 PENTYL 3 OL; ALCOHOL; ALKYL GROUP; ALKYNE; ALUMINUM; BIS CYCLOPROPANE DERIVATIVE; CYCLOPROPANE DERIVATIVE; METHYLENE IODIDE; PROPARGYLIC ALCOHOL; REAGENT; TRIALKYLALUMINUM; UNCLASSIFIED DRUG;

EID: 66149160250     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.04.114     Document Type: Article
Times cited : (14)

References (22)
  • 15
    • 66149165697 scopus 로고    scopus 로고
    • note
    • 2. The solvent was removed under reduced pressure and the residue distilled to yield 0.40 g of an oily product (69% isolated yield, 77% GC yield). Bp 67-70 °C (1 Torr).
  • 16
    • 66149164296 scopus 로고    scopus 로고
    • note
    • 26: C, 86.52; H, 13.48. Found: C, 86.89; H, 13.11.{A figure is presented}
  • 20
    • 66149165698 scopus 로고    scopus 로고
    • note
    • In the case of 1-ethynylcyclohexanol, deuterolysis of the reaction mixture did not result in 1-(deuteroethynyl)cyclohexanol which indicates that metallation processes can be excluded from consideration.
  • 21
    • 66149172002 scopus 로고    scopus 로고
    • note
    • 2 was 73% after 2 h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.