메뉴 건너뛰기




Volumn 13, Issue 6, 2007, Pages 1784-1795

Asymmetric synthesis of 3-oxa-15-deoxy-16-(m-tolyl)-17,18,19,20- tetranorisocarbacyclin and its neuroprotective analogue 15-deoxy-16-(m-tolyl)- 17,18,19,20-tetranorisocarbacyclin based on the conjugate addition-azoalkene- asymmetric olefination strategy

Author keywords

Asymmetric synthesis; Isocarbacyclins; Medicinal chemistry; Olefination; Prostacyclin receptor

Indexed keywords

ADDITION REACTIONS; CONJUGATED POLYMERS; KETONES; METABOLISM; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 34250658740     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200600728     Document Type: Article
Times cited : (25)

References (89)
  • 1
    • 0004242617 scopus 로고
    • Eds, J. R. Vane, S. Bergström, Raven Press, New York
    • Prostacyclin (Eds.: J. R. Vane, S. Bergström), Raven Press, New York, 1979.
    • (1979) Prostacyclin
  • 2
    • 34250659802 scopus 로고    scopus 로고
    • Prostacyclin and its Stable Analogue lloprost (Eds. : R. J. Gryglewski, G. Stock), Springer-Verlag, Berlin, 1987.
    • Prostacyclin and its Stable Analogue lloprost (Eds. : R. J. Gryglewski, G. Stock), Springer-Verlag, Berlin, 1987.
  • 41
    • 34250621855 scopus 로고    scopus 로고
    • M. Suzuki, H. Doi, T. Hosoya, Y. Watanabe, Seibutsu Butsuri 2004, 44.265-270.
    • M. Suzuki, H. Doi, T. Hosoya, Y. Watanabe, Seibutsu Butsuri 2004, 44.265-270.
  • 51
    • 28144456412 scopus 로고    scopus 로고
    • M. Dib, Drugs 2005, 65, 2463-2479.
    • (2005) Drugs , vol.65 , pp. 2463-2479
    • Dib, M.1
  • 55
    • 4444289966 scopus 로고    scopus 로고
    • Population Division, DESA, United Nations, New York
    • World Population Ageing: 1950-2050, Population Division, DESA, United Nations, New York, 2001.
    • (2001) World Population Ageing: 1950-2050
  • 61
    • 34250668437 scopus 로고
    • Abstr
    • [Chem. Abstr. 1983, 98, 53513];
    • (1983) , vol.98 , pp. 53513
    • Chem1
  • 63
    • 34250622509 scopus 로고
    • Abstr
    • [Chem. Abstr. 1984, 101, 6931].
    • (1984) , vol.101 , pp. 6931
    • Chem1
  • 70
    • 0025145919 scopus 로고    scopus 로고
    • For a synthesis of isocarbacyclin featuring the conjugate addition of a C13-C20 alkenylcopper building block to a cyclopentenone derivative and a stepwise construction of the bicyclic ring skeleton, see: K. Bannai, T. Tanaka, N. Okamura, A. Hazato, S. Sugiura, K. Manabe, K. Tomimori, Y. Kato, S. Kurozumi, R. Noyori, Tetrahedron 1990, 46, 6689-6704.
    • For a synthesis of isocarbacyclin featuring the conjugate addition of a C13-C20 alkenylcopper building block to a cyclopentenone derivative and a stepwise construction of the bicyclic ring skeleton, see: K. Bannai, T. Tanaka, N. Okamura, A. Hazato, S. Sugiura, K. Manabe, K. Tomimori, Y. Kato, S. Kurozumi, R. Noyori, Tetrahedron 1990, 46, 6689-6704.
  • 77
    • 0035477040 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 3667-3670.
    • (2001) Chem. Int. Ed , vol.40 , pp. 3667-3670
    • Angew1
  • 78
    • 0000349575 scopus 로고    scopus 로고
    • The synthesis of alkenyl iodide 21 through hydroboration of alkyne 20 with catecholborane and iodination of the corresponding E-configured alkenyl boronic acid with iodine (H. C. Brown, T. Hamaoka, S. K. Ravindran, J. Am. Chem. Soc. 1973, 95, 5786-5788) gave a mixture of 21 and its Z isomer in a ratio of 91:9, see M. van de Sande, Ph.D. Thesis, RWTH Aachen, 2006.
    • The synthesis of alkenyl iodide 21 through hydroboration of alkyne 20 with catecholborane and iodination of the corresponding E-configured alkenyl boronic acid with iodine (H. C. Brown, T. Hamaoka, S. K. Ravindran, J. Am. Chem. Soc. 1973, 95, 5786-5788) gave a mixture of 21 and its Z isomer in a ratio of 91:9, see M. van de Sande, Ph.D. Thesis, RWTH Aachen, 2006.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.