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Volumn 26, Issue 7, 2005, Pages 1112-1116

Synthesis of 9-oxo-9,13b-dihydro-7H-benzo[3,4]azepino[2,1-a]isoindole-6- carboxylic acid derivatives from Baylis-Hillman adducts

Author keywords

Baylis Hillman adducts; Benzo 3,4 azepino 2,1 a isoindole; N acyliminium salts

Indexed keywords


EID: 23744447409     PISSN: 02532964     EISSN: None     Source Type: Journal    
DOI: 10.5012/bkcs.2005.26.7.1112     Document Type: Article
Times cited : (10)

References (44)
  • 1
    • 16444374364 scopus 로고    scopus 로고
    • For our recent publications on the synthesis of heterocyclic compounds by using the Baylis-Hillman adducts, see (a) Lee, C. G.; Lee, K. Y.; Kim, S. C.; Kim, J. N. Bull Korean Chem. Soc. 2005, 26, 485.
    • (2005) Bull Korean Chem. Soc. , vol.26 , pp. 485
    • Lee, C.G.1    Lee, K.Y.2    Kim, S.C.3    Kim, J.N.4
  • 32
    • 0028824251 scopus 로고
    • For the synthesis of phorbol derivatives by the combination of Baylis-Hillman chemistry and N-acyliminium ion chemistry, see (a) Marson, C. M.; Pink, J. H.; Smith, C. Tetrahedron Lett. 1995, 36, 8107.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 8107
    • Marson, C.M.1    Pink, J.H.2    Smith, C.3
  • 34
  • 44
    • 23744446212 scopus 로고    scopus 로고
    • note
    • 2O to the sample, OH peak disappeared and the proton of the phthalimide moiety was converted as a singlet.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.