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Volumn 64, Issue 22, 1999, Pages 8342-8349

Stereoselective solid-phase synthesis of a triaza tricyclic ring system: A new chemotype for lead discovery

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; HYDANTOIN; PYRROLIDINE DERIVATIVE; RESIN;

EID: 0033615680     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990969+     Document Type: Article
Times cited : (37)

References (69)
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    • note
    • One may distinguish synthetic strategies in which the natural product template is assembled de novo by solid-phase methods (as in ref 1) from those in which a key scaffold building block is preformed in solution and then attached to resin for subsequent elaboration (vide infra). For antibacterial natural product derivatives, see:
  • 23
    • 0031994805 scopus 로고    scopus 로고
    • For a review of carbohydrate synthesis by polymer-supported methods, see: Sofia, M. J. Mol. Diversity 1998, 3, 75.
    • (1998) Mol. Diversity , vol.3 , pp. 75
    • Sofia, M.J.1
  • 31
    • 0001625454 scopus 로고
    • Curran D. P., Ed.; JAI Press: Greenwich, CT
    • Grigg, R.; Sridharan, V. In Advances in Cycloaddition; Curran D. P., Ed.; JAI Press: Greenwich, CT, 1993; Vol. 3, p 161.
    • (1993) Advances in Cycloaddition , vol.3 , pp. 161
    • Grigg, R.1    Sridharan, V.2
  • 32
    • 0000629986 scopus 로고
    • Intermolecular 1,3-dipolar cycloadditions
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (b) Padwa, A. Intermolecular 1,3-Dipolar Cycloadditions. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. IV, p 1069.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1069
    • Padwa, A.1
  • 33
  • 40
    • 0000629986 scopus 로고
    • Intramolecular 1,3-dipolar cycloadditions
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • Wade, P. A. Intramolecular 1,3-Dipolar Cycloadditions. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. IV, p 1069.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1069
    • Wade, P.A.1
  • 59
    • 0030936620 scopus 로고    scopus 로고
    • For solid-phase adaptations of the Fukuyama amine synthesis, see: (a) Miller, S. C.; Scanlon, T. S. J. Am. Chem. Soc. 1997, 119, 2301.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2301
    • Miller, S.C.1    Scanlon, T.S.2
  • 69
    • 0033515461 scopus 로고    scopus 로고
    • For a recent report of an optimized protocol for reductive alkylation of polymer-supported substrates, see: Schwarz, M. K.; Tumelty, D.; Gallop, M. A. J. Org. Chem. 1999, 64, 2219.
    • (1999) J. Org. Chem. , vol.64 , pp. 2219
    • Schwarz, M.K.1    Tumelty, D.2    Gallop, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.