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Volumn 51, Issue 13, 2010, Pages 1666-1670

Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE; ALCOHOL DERIVATIVE; ALDEHYDE; ALKADIENE; BUTYLTELLURO 4 METHOXY 1,3 BUTADIENE; DECA (2E,4E) DIENAL; DECANOIC ACID; LITHIUM; METHYL (2E,4E) DECADIENOATE; METHYLTRIPHENYLPHOSPHORANE; PHOSPHORANE DERIVATIVE; SEX PHEROMONE; TELLURIUM; TRIENE; UNCLASSIFIED DRUG; UNDECA (1,3E,5E) TRIENE;

EID: 77149138638     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.01.066     Document Type: Article
Times cited : (9)

References (100)
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    • Heinz D.E., and Jennings W.G. J. Food Sci. 31 (1966) 69 (Chem. Abstr. 1966, 64, 11769f)
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    • Heinz, D.E.1    Jennings, W.G.2
  • 13
    • 77149148139 scopus 로고    scopus 로고
    • note
    • 20 atoms.
  • 85
    • 85013347101 scopus 로고
    • and references cited therein
    • Borer B.C., and Taylor R.J.K. Synlett (1992) 117 and references cited therein
    • (1992) Synlett , pp. 117
    • Borer, B.C.1    Taylor, R.J.K.2
  • 89
    • 77149130938 scopus 로고    scopus 로고
    • note
    • 43
  • 90
    • 77149150618 scopus 로고    scopus 로고
    • note
    • 16OTe: C, 40.36; H, 6.02. Found: C, 40.73; H, 5.99.
  • 91
    • 77149141408 scopus 로고    scopus 로고
    • note
    • 2, BuLi (0.76 ml, 1.1 mmol, 1.43 M) was added in one portion. The reaction mixture was stirred at this temperature and after 1.0 min, the butadienyl lithium 3 formed can be used in situ. The observations of the reactions of this intermediate (total disappearance of 9 followed by TLC and formation of only one product) indicated that it is formed in high yield.
  • 92
    • 77149139490 scopus 로고    scopus 로고
    • note
    • 3): 13.78, 22.41, 27.40, 36.88, 59.80, 67.53, 101.73, 121.84, 130.70, 148.23.
  • 93
    • 77149151577 scopus 로고    scopus 로고
    • note
    • f (pentene-dichloromethane 1:1) 0.48, UV active.
  • 94
    • 77149126749 scopus 로고    scopus 로고
    • note
    • max (hexane) 252, 262, 272 nm.
  • 95
    • 77149128676 scopus 로고    scopus 로고
    • note
    • 4, 100%), 183 (M+H, 25).
  • 97
    • 77149174192 scopus 로고    scopus 로고
    • note
    • 1,2 = 16.7 Hz, 2-H).
  • 98
    • 77149165107 scopus 로고    scopus 로고
    • note
    • max (hexane) 252, 262, 272 nm.
  • 99
    • 77149154352 scopus 로고    scopus 로고
    • note
    • max (hexane) 252, 262, 272 nm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.