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Volumn 67, Issue 27-28, 2011, Pages 5107-5124

On the choice of Lewis acids for the Prins reaction; two total syntheses of (±)-Civet

Author keywords

Civet; Dihydropyran; Fluorinated pyran; Lewis acid; Mukaiyama Aldol silyl Prins reaction; Prins reaction; Pyran; Silyl Prins reaction

Indexed keywords

CIVET; DIHYDROPYRAN DERIVATIVE; LEWIS ACID; PERFUME; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79958764494     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.05.019     Document Type: Article
Times cited : (51)

References (57)
  • 15
    • 34848899797 scopus 로고    scopus 로고
    • This paper does include one example of a tertiary carbcation, formed from a Nicholas-Prins cyclisationd, being trapped by the triflate anion, although all the examples cited currently involve secondary carbocations
    • Olier, C.; Gastaldi, S.; Gilb, G.; Bertrand, M. P. Tetrahedron Lett. 2007, 48, 7801-7804. This paper does include one example of a tertiary carbcation, formed from a Nicholas-Prins cyclisationd, being trapped by the triflate anion, although all the examples cited currently involve secondary carbocations.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 7801-7804
    • Olier, C.1    Gastaldi, S.2    Gilb, G.3    Bertrand, M.P.4
  • 49
    • 79958742961 scopus 로고    scopus 로고
    • note
    • p-Anisaldehyde Stain: This stain is an excellent multipurpose visualization method for examining TLC plates for oxygenated compounds. Preparation: To 135 ml of absolute ethanol was added 5 ml of concentrated sulfuric acid, 1.5 ml of glacial acetic acid and 3.7 ml of p-anisaldehyde. The solution is then stirred vigorously to ensure homogeneity. The resulting staining solution is ideally stored in a 100 ml wide mouth jar covered with aluminum foil.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.