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Volumn 4, Issue 4, 2002, Pages 565-568

An efficient organometallic approach to new carbocyclic nucleoside analogues

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC ANTIBIOTIC; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; NUCLEOSIDE; ORGANOMETALLIC COMPOUND;

EID: 0037149069     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol017181+     Document Type: Article
Times cited : (28)

References (46)
  • 5
    • 0034725386 scopus 로고    scopus 로고
    • and references therein
    • For recent work on the synthesis of carbocyclic nudeoside analogues, see: (a) Trost, B. M.; Madsen, R.; Guile, S. D.; Brown, B. J. Am. Chem. Soc. 2000, 122, 5947 and references therein.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5947
    • Trost, B.M.1    Madsen, R.2    Guile, S.D.3    Brown, B.4
  • 19
    • 0000117791 scopus 로고    scopus 로고
    • Egli, M. Angew. Chem., Int. Ed Engl. 1996, 35, 1895; Angew. Chem. 1996, 108, 2021.
    • (1996) Angew. Chem. , vol.108 , pp. 2021
  • 22
    • 0031971911 scopus 로고    scopus 로고
    • (b) Geis, O.; Schmalz, H.-G. Angew. Chem. 1998, 110, 955; Angew. Chem., Int. Ed. 1998, 37, 911.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 911
  • 23
    • 0000213863 scopus 로고    scopus 로고
    • Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim
    • (c) Jeong, N. In Transition Metals in Organic Synthesis; Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998; Vol. I, p 560.
    • (1998) Transition Metals in Organic Synthesis , vol.1 , pp. 560
    • Jeong, N.1
  • 27
    • 0001216151 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin
    • (a) Buchwald, S. L.; Hicks, F. A. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 2, p 491.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 491
    • Buchwald, S.L.1    Hicks, F.A.2
  • 37
    • 0042822616 scopus 로고    scopus 로고
    • note
    • 4f
  • 38
    • 0027299437 scopus 로고
    • The relative configuration of rac-12 was determined by NMR-NOE measurements. For a related but less practical synthesis of compound rac-12, see: Jeong, N.; Lee, B. Y.; Lee, S. M.; Chung, Y. K.; Lee, S.-G. Tetrahedron Lett. 1993, 34, 4023.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 4023
    • Jeong, N.1    Lee, B.Y.2    Lee, S.M.3    Chung, Y.K.4    Lee, S.-G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.