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Volumn 5, Issue 5, 2003, Pages 606-609

Solution-phase parallel Wittig olefination: Synthesis of substituted 1,2-diarylethanes

Author keywords

[No Author keywords available]

Indexed keywords

ALKANE DERIVATIVE; SARPOGRELATE; SEROTONIN 2A AGONIST;

EID: 0141795489     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc0300210     Document Type: Article
Times cited : (14)

References (17)
  • 4
    • 0021319809 scopus 로고
    • Besides antipsychotic activity, 1,2-diarylethanes are known anticonvulsants and have shown antithrombotic activity. See: (a) Kikumoto, R.; Tobe, A.; Fukami, H.; Ninomiya, K.; Egawa, M. J. Med. Chem. 1984, 27, 645-649. (b) Kikumoto, R.; Hara, H.; Ninomiya, K.; Osakabe, M.; Sugano, M.; Fukami, H.; Yoshikuni, T. J. Med. Chem. 1990, 33, 1818-1823.
    • (1984) J. Med. Chem. , vol.27 , pp. 645-649
    • Kikumoto, R.1    Tobe, A.2    Fukami, H.3    Ninomiya, K.4    Egawa, M.5
  • 5
    • 0025370777 scopus 로고
    • Besides antipsychotic activity, 1,2-diarylethanes are known anticonvulsants and have shown antithrombotic activity. See: (a) Kikumoto, R.; Tobe, A.; Fukami, H.; Ninomiya, K.; Egawa, M. J. Med. Chem. 1984, 27, 645-649. (b) Kikumoto, R.; Hara, H.; Ninomiya, K.; Osakabe, M.; Sugano, M.; Fukami, H.; Yoshikuni, T. J. Med. Chem. 1990, 33, 1818-1823.
    • (1990) J. Med. Chem. , vol.33 , pp. 1818-1823
    • Kikumoto, R.1    Hara, H.2    Ninomiya, K.3    Osakabe, M.4    Sugano, M.5    Fukami, H.6    Yoshikuni, T.7
  • 10
    • 0035937306 scopus 로고    scopus 로고
    • For examples, see: (a) Charette, A. B.; Janes, M. K.; Boezio, A. A. J. Org. Chem. 2001, 66, 2178-2180. (b) Pelletier, J. C.; Kincaid, S. Tetrahedron Lett. 2000, 41, 797-800. (c) Tunoori, A. R.; Dutte, D.; Georg, G. I. Tetrahedron Lett. 1998, 39, 8751-8754.
    • (2001) J. Org. Chem. , vol.66 , pp. 2178-2180
    • Charette, A.B.1    Janes, M.K.2    Boezio, A.A.3
  • 11
    • 0034606936 scopus 로고    scopus 로고
    • For examples, see: (a) Charette, A. B.; Janes, M. K.; Boezio, A. A. J. Org. Chem. 2001, 66, 2178-2180. (b) Pelletier, J. C.; Kincaid, S. Tetrahedron Lett. 2000, 41, 797-800. (c) Tunoori, A. R.; Dutte, D.; Georg, G. I. Tetrahedron Lett. 1998, 39, 8751-8754.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 797-800
    • Pelletier, J.C.1    Kincaid, S.2
  • 12
    • 0032569908 scopus 로고    scopus 로고
    • For examples, see: (a) Charette, A. B.; Janes, M. K.; Boezio, A. A. J. Org. Chem. 2001, 66, 2178-2180. (b) Pelletier, J. C.; Kincaid, S. Tetrahedron Lett. 2000, 41, 797-800. (c) Tunoori, A. R.; Dutte, D.; Georg, G. I. Tetrahedron Lett. 1998, 39, 8751-8754.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8751-8754
    • Tunoori, A.R.1    Dutte, D.2    Georg, G.I.3
  • 13
    • 0001104765 scopus 로고    scopus 로고
    • For examples, see: (a) Westman, J. Org. Lett. 2001, 3, 3745-3747. (b) Sieber, F.; Wentworth, P., Jr.; Toker, J. D.; Wentworth, A. D.; Metz, W. A.; Reed, N. N.; Janda, K. D. J. Org. Chem. 1999, 64, 5188-5192.
    • (2001) Org. Lett. , vol.3 , pp. 3745-3747
    • Westman, J.1
  • 16
    • 0141703133 scopus 로고    scopus 로고
    • U.S. Patent 5,707,798; 1998
    • R-SAT is a mammalian cell-based assay technology that provides a sensitive measure of receptor function. Brann, M. R. U.S. Patent 5,707,798; 1988. Chem. Abstr. 1998, 128, 111548.
    • Brann, M.R.1
  • 17
    • 0007321318 scopus 로고    scopus 로고
    • R-SAT is a mammalian cell-based assay technology that provides a sensitive measure of receptor function. Brann, M. R. U.S. Patent 5,707,798; 1988. Chem. Abstr. 1998, 128, 111548.
    • (1998) Chem. Abstr. , vol.128 , pp. 111548


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.