메뉴 건너뛰기




Volumn 26, Issue 52, 1985, Pages 6423-6426

Synthesis of 7,8-acetylenic analogs of hexahydro leukotriene-E4 with agonist and antagonist activities: convenient stereoselective routes to E- and Z-enynes

Author keywords

[No Author keywords available]

Indexed keywords

7 [3 (4 ACETYL 3 HYDROXY 2 PROPYLPHENOXY) 2 HYDROXYPROPOXY] 4 OXO 8 PROPYL 4H 1 BENZOPYRAN 2 CARBOXYLIC ACID; LEUKOTRIENE E4; LEUKOTRIENE E4 DERIVATIVE;

EID: 0022397622     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)99017-8     Document Type: Article
Times cited : (12)

References (30)
  • 11
    • 0000666413 scopus 로고
    • Hydrophobic binding of the hydrocarbon chains do not seem to explain this result since dehydrations in the presence of urea (in dioxane) did not alter the Z:E ratio in favor of E-enynes;
    • (1968) J.A.C.S. , vol.90 , pp. 1875
    • Menger1    Portonoy2
  • 14
    • 0000438404 scopus 로고
    • Regio- and stereoselective synthesis of -1,3-enynes via coupling of nucleophiles with 1-[(alkynyl) dicobalt hexacarbonyl]allyl cations
    • (1982) Tetrahedron Letters , pp. 2555
    • Padmanabhan1    Nicholas2
  • 16
    • 0003591347 scopus 로고
    • Ouverture acide d'alcoolsαcyclopropaniquesα'acetyleniques complexes par le dicobalt-octacarbony le. Obtention stereoselective d'enynes conjugues E, precurseurs de dienes conjugues E, Z.
    • (1976) Tetrahedron Letters , pp. 745
    • Descoins1    Samain2
  • 17
    • 84918429877 scopus 로고    scopus 로고
    • D + 35.2° (dioxane).
  • 19
    • 0020458281 scopus 로고
    • Total synthesis of 5-desoxyleukotriene D. A new and useful equivalent of the 4-formyl-, -1,3-butadienyl anion
    • (1982) Tetrahedron Letters , pp. 3463
    • Corey1    Hoover2
  • 23
    • 0006352508 scopus 로고
    • 2 according to, Unlike the mesylate 7a, the bromides of the type 7b were stable to manipulations at room temperature.
    • (1963) J. Chem. Soc. , pp. 2559
    • Crofts1    Downie2
  • 24
    • 33847087351 scopus 로고
    • Reduction of .alpha.,.beta.-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane. High asymmetric induction in aliphatic systems
    • 3) 9a.
    • (1980) Journal of the American Chemical Society , vol.102 , pp. 867
  • 26
    • 84918429876 scopus 로고    scopus 로고
    • 11b gave only a 10% yield of 12 (R″=H) besides unchanged 18 (R″=Me).
  • 27
    • 84918429875 scopus 로고    scopus 로고
    • 4 induced contractions.
  • 30
    • 84918429873 scopus 로고    scopus 로고
    • Satisfactory IR, PMR, CMR, and MS (EI and FAB) were obtained for all new compounds.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.