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Volumn 45, Issue 10, 2004, Pages 2197-2201

A new strategy of tandem transetherification-intramolecular hetero Diels-Alder reaction with (E,Z)-mixture of ethyl 2-nitro-3-ethoxyacrylate and δ,ε-unsaturated alcohols leading to functionalized trans-fused bicyclic nitronates

Author keywords

Intramolecular hetero Diels Alder reaction; Lewis acid; Nitroalkene; Tandem reaction; Transetherification; , Unsaturated alcohols

Indexed keywords

ACRYLIC ACID DERIVATIVE; ALCOHOL; LEWIS ACID; NITRO DERIVATIVE;

EID: 1242317857     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.01.026     Document Type: Article
Times cited : (7)

References (20)
  • 12
    • 0036944114 scopus 로고    scopus 로고
    • and references cited therein
    • Denmark S.E., Juhl M. Helv. Chim. Acta. 85:2002;3712-3736. and references cited therein.
    • (2002) Helv. Chim. Acta , vol.85 , pp. 3712-3736
    • Denmark, S.E.1    Juhl, M.2
  • 14
    • 0003056752 scopus 로고
    • Unsaturated alcohols
    • Unsaturated alcohols 2-10 were prepared from the corresponding unsaturated carbonyls: Cresson P. Bull. Soc. Chim. Fr. 1964;2618-2628.
    • (1964) Bull. Soc. Chim. Fr. , pp. 2618-2628
    • Cresson, P.1
  • 17
    • 85030907971 scopus 로고    scopus 로고
    • note
    • + 258.1341, found 258.1334.
  • 20
    • 85030901027 scopus 로고    scopus 로고
    • note
    • Intramolecular cycloaddition reaction by using transetherified intermediates A and/or B themselves could not be examined because of their decomposition during the separation by silica gel column chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.