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Volumn 54, Issue 32, 1998, Pages 9303-9316

Stereocontrolled and enantioselective synthesis of the branched 6- amino-4,6-deoxyheptopyranuronic acid component of amipurimycin

Author keywords

Amino acids and derivatives; Asymmetric synthesis; Carbohydrates; Stereocontrol

Indexed keywords

2 (2,2 DIMETHYL 3 TERT BUTOXYCARBONYL 1,3 OXAZOLIDIN 4 YL) 5 ACETYLOXY 2,3 DIHYDROPYRAN 4 ONE; 6 AMINO 4,6 DEOXYHEPTOPYRANURONIC ACID; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032490928     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00585-7     Document Type: Article
Times cited : (23)

References (31)
  • 15
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    • [9] For a reviews of the synthesis of complex nucleoside antibiotics, see: [a] Knapp, S. Chem. Rev. 1995, 95, 1859-1876.
    • (1995) Chem. Rev. , vol.95 , pp. 1859-1876
    • Knapp, S.1
  • 16
    • 0003373977 scopus 로고
    • Synthetic approaches to complex nucleoside antibiotics
    • Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, Part A
    • [b] Garner, P. Synthetic Approaches to Complex Nucleoside Antibiotics. In Studies in Natural Product Chemistry; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1988; Part A, Vol. 1. pp 397-434.
    • (1988) Studies in Natural Product Chemistry , vol.1 , pp. 397-434
    • Garner, P.1
  • 27
    • 0010496297 scopus 로고
    • See references [6a] and [6c] as well
    • [b] Dyong, I.; Weigand, J.; Meyer, W. Tetrahedron Lett. 1981, 22, 2969-2972. See references [6a] and [6c] as well.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 2969-2972
    • Dyong, I.1    Weigand, J.2    Meyer, W.3
  • 29
    • 0010455482 scopus 로고    scopus 로고
    • note
    • [20] Inquiries concerning this X-ray structure determination should be addressed to W. J. Y. at the Department of Chemistry, The University of Akron, Akron, OH 44325-3601. The atomic coordinates and thermal parameters for compound 31 will be deposited with the Cambridge Crystallographic Data Centre. These coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre. 12 Union Road, Cambridge, CB2 1EZ, UK.
  • 30
    • 0004297694 scopus 로고
    • American Chemical Society: Washington, DC
    • [21] The numbering system used in this paper corresponds to the current CA index names for substructures i-iii. For details, see: Chemical Abstracts Service Index Guide; American Chemical Society: Washington, DC, 1989. (figure presented)
    • (1989) Chemical Abstracts Service Index Guide
  • 31
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    • Organic syntheses
    • Blatt, A. H. E.; Wiley: New York. Note 3
    • [22] Arndt, F. In Organic Syntheses; Blatt, A. H. E.; Wiley: New York. 1943; Collect. Vol. 2, pp 165-167, Note 3.
    • (1943) Collect. , vol.2 , pp. 165-167
    • Arndt, F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.