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Volumn 41, Issue 11, 2000, Pages 1721-1724

Toward the synthesis of pamamycin-607

Author keywords

Antibiotics; Desulfurization; Diels Alder reactions; Sultones

Indexed keywords

MACROLIDE; PAMAMYCIN 607; UNCLASSIFIED DRUG;

EID: 0034635845     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00022-8     Document Type: Article
Times cited : (33)

References (32)
  • 5
    • 0030860279 scopus 로고    scopus 로고
    • For an efficient kinetic resolution of racemic terminal epoxides, see:
    • For an efficient kinetic resolution of racemic terminal epoxides, see: Tokunaga, M.; Larrow, J. F.; Kakiuchi, F.; Jacobsen, E. N. Science 1997, 277, 936-938.
    • (1997) Science , vol.277 , pp. 936-938
    • Tokunaga, M.1    Larrow, J.F.2    Kakiuchi, F.3    Jacobsen, E.N.4
  • 27
    • 0342518724 scopus 로고    scopus 로고
    • (b) We prepared (S)-1,2-epoxypentane from racemic 1,2-epoxypentane using the procedure given in Ref. 3 (>99% ee determined by capillary GC at the stage of 7)
    • (b) We prepared (S)-1,2-epoxypentane from racemic 1,2-epoxypentane using the procedure given in Ref. 3 (>99% ee determined by capillary GC at the stage of 7).
  • 29
    • 0342518723 scopus 로고    scopus 로고
    • unpublished results.
    • Wang, Y.; Metz P., unpublished results.
    • Wang, Y.1    Metz, P.2
  • 31
    • 0343388356 scopus 로고    scopus 로고
    • Crystallographic data of 14 have been deposited with the Cambridge Crystallographic Data Centre.
    • Crystallographic data of 14 have been deposited with the Cambridge Crystallographic Data Centre.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.