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Volumn 51, Issue 13, 2010, Pages 1710-1712

Synthesis of farinomalein

Author keywords

[No Author keywords available]

Indexed keywords

BUTENOLIDE; FARINOMALEIN; GAMMA HYDROXYBUTENOLIDE; MALEIMIDE; UNCLASSIFIED DRUG;

EID: 76949104687     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.01.083     Document Type: Article
Times cited : (23)

References (32)
  • 21
    • 3142666213 scopus 로고    scopus 로고
    • note
    • 3, 100 MHz) δ 174.3, 172.8, 171.8, 116.9, 94.5, 51.7, 40.7, 35.2, 27.9, 21.3, 20.1. Not only were the coupling patterns more consistent with the proposed structure 5, but also the γ-carbon resonated at δ 94.5, which is ∼10 ppm higher than the expected carbon shift for the γ-carbon of a compound such as 3. See: Mangaleswaran, S.; Argade, N. P. Synthesis 2004, 1560-1562.
  • 30
    • 76949093795 scopus 로고    scopus 로고
    • note
    • C 49.1) as done in Ref. 1.
  • 31
    • 76949101734 scopus 로고    scopus 로고
    • note
    • 13C NMR. In addition, the values for the downfield carbons did not match the literature report, which we attribute to concentration effects.
  • 32
    • 33745909372 scopus 로고    scopus 로고
    • The oxidation of methyl lambertianate, a naturally occurring 3-substituted furan, to the corresponding anhydride followed by the reaction of primary amines is a closely related strategy for the synthesis of maleimides.
    • The oxidation of methyl lambertianate, a naturally occurring 3-substituted furan, to the corresponding anhydride followed by the reaction of primary amines is a closely related strategy for the synthesis of maleimides. Kharitonov Y.V., Shul'ts E.E., Shakirov M.M., and Tolstikov G.A. Russ. J. Org. Chem. 42 (2006) 707-718
    • (2006) Russ. J. Org. Chem. , vol.42 , pp. 707-718
    • Kharitonov, Y.V.1    Shul'ts, E.E.2    Shakirov, M.M.3    Tolstikov, G.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.