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Volumn 28, Issue 12, 2007, Pages 2501-2504

Synthesis of isochroman and tetrahydroisoquinoline derivatives from Baylis-Hillman adducts by radical cyclization

Author keywords

Baylis Hillman adducts; Isochroman; Radical cyclization; Tetrahydroisoquinoline

Indexed keywords


EID: 38049101333     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2007.28.12.2501     Document Type: Article
Times cited : (8)

References (37)
  • 1
    • 34248672252 scopus 로고    scopus 로고
    • For our recent papers on the radical cyclizations using modified Baylis-Hillman adducts, see: a
    • For our recent papers on the radical cyclizations using modified Baylis-Hillman adducts, see: (a) Gowrisankar, S.; Kim, S. J.; Lee, J.-E.; Kim, J. N. Tetrahedron Lett. 2007, 48, 4419-4422.
    • (2007) Tetrahedron Lett , vol.48 , pp. 4419-4422
    • Gowrisankar, S.1    Kim, S.J.2    Lee, J.-E.3    Kim, J.N.4
  • 8
    • 0035830480 scopus 로고    scopus 로고
    • For the synthesis and biological activities of isochroman moiety-containing compounds, see: a
    • For the synthesis and biological activities of isochroman moiety-containing compounds, see: (a) Clive, D. L. J.; Sannigrahi, M.; Hisaindee, S. J. Org. Chem. 2001, 66, 954-961.
    • (2001) J. Org. Chem , vol.66 , pp. 954-961
    • Clive, D.L.J.1    Sannigrahi, M.2    Hisaindee, S.3
  • 13
    • 0016915864 scopus 로고
    • For the synthesis and biological activities of tetrahydroisoquinoline moiety-containing compounds, see: a
    • For the synthesis and biological activities of tetrahydroisoquinoline moiety-containing compounds, see: (a) Smissman, E. E.; Reid, J. R.; Walsh, D. A. J. Med. Chem. 1976, 19, 127-131.
    • (1976) J. Med. Chem , vol.19 , pp. 127-131
    • Smissman, E.E.1    Reid, J.R.2    Walsh, D.A.3
  • 23
    • 33746911128 scopus 로고    scopus 로고
    • For the synthesis and biological activities of isochromans and tetrahydroisoquinolines having methylene dioxy moiety, see: (a) Fishlock, D, Williams, R. M. Org. Lett. 2006, 8, 3299-3301
    • For the synthesis and biological activities of isochromans and tetrahydroisoquinolines having methylene dioxy moiety, see: (a) Fishlock, D.; Williams, R. M. Org. Lett. 2006, 8, 3299-3301.
  • 29
    • 33748780647 scopus 로고    scopus 로고
    • For the radical cyclizations involving Baylis-Hillman adducts, see: a
    • For the radical cyclizations involving Baylis-Hillman adducts, see: (a) Singh, V.; Batra, S. Tetrahedron Lett. 2006, 47, 7043-7045.
    • (2006) Tetrahedron Lett , vol.47 , pp. 7043-7045
    • Singh, V.1    Batra, S.2
  • 35
    • 4644307321 scopus 로고    scopus 로고
    • Synthesis of starting materials 1b and 1c, please see: (a) Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2004, 25, 413-414.
    • Synthesis of starting materials 1b and 1c, please see: (a) Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2004, 25, 413-414.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.