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Volumn 28, Issue 30, 1987, Pages 3463-3466

Synthetic studies towards halichondrins

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000895818     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)96327-5     Document Type: Article
Times cited : (83)

References (19)
  • 5
    • 84918483134 scopus 로고    scopus 로고
    • The substances reported in this paper belong to the antipodes of halichondrins. The drawings are, however, made in the same absolute configurations as that of halichondrins.
  • 6
    • 84918483133 scopus 로고    scopus 로고
    • Satisfactory spectroscopic data were obtained for all the new compounds reported in this paper.
  • 7
    • 0342885320 scopus 로고
    • 2O/RT. Transformation of 1,6-anhydro-D-galactose 3,4-acetonide into 1,6-anhydro-D-talose 3,4-acetonide is known
    • (1968) Carbohydr. Res. , vol.7 , pp. 474
    • Hughes1
  • 11
    • 84918483132 scopus 로고    scopus 로고
    • With respect to the anisylidene moiety, a single stereoisomer was formed.
  • 15
    • 84918483131 scopus 로고    scopus 로고
    • This cyclization was also effected on silica gel.
  • 16
    • 84918483130 scopus 로고    scopus 로고
    • 1b are well compared with those of 13:
  • 17
    • 84918483129 scopus 로고    scopus 로고
    • Attempted cyclization of the methyl ester corresponding to 14 did not yield promising results.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.