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Volumn 45, Issue 17, 2004, Pages 3339-3340

Iridodials: Enantiospecific synthesis and stereochemical assignment of the pheromone for the golden-eyed lacewing, Chrysopa oculata

Author keywords

Iridodials; Lacewing; Nepetalactone

Indexed keywords

IRIDODIAL; LACTONE DERIVATIVE; OIL; PHEROMONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1842636711     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.03.034     Document Type: Article
Times cited : (24)

References (17)
  • 3
    • 0012994244 scopus 로고
    • Biological Control in the Field
    • M. Canard, Y. Semeria, & T.R. New. The Hague: Dr. W. Junk Publishers
    • Ridgway R.L., Murphy W.L. Biological Control in the Field. Canard M., Semeria Y., New T.R. Biology of Chrysopidae. 1984;220-228 Dr. W. Junk Publishers, The Hague.
    • (1984) Biology of Chrysopidae , pp. 220-228
    • Ridgway, R.L.1    Murphy, W.L.2
  • 13
    • 1842646353 scopus 로고    scopus 로고
    • note
    • Ethyl acetate (5%) in hexane as mobile phase and 230-400 mesh silica gel as stationary phase.
  • 14
    • 1842747093 scopus 로고    scopus 로고
    • note
    • 3, 75 MHz) δ 204.5 (C6), 106.8 (C9), 64.9 (C11), 64.7 (C12), 60.41 (C1), 44.0 (C8), 36.9 (C2), 35.3 (C5), 32.9 (C3), 30.6 (C4), 21.4 (C7), and 13.7 (C10) ppm.
  • 16
    • 1842747088 scopus 로고    scopus 로고
    • note
    • Since iridodial isomers were derived from nepetalactone 2a and 2b, the absolute configuration remain intact for 7a, 7, and 4a positions of origin (which was established earlier by Dawson et al.).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.