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Volumn 6, Issue 8, 2008, Pages 1478-1497

Total synthesis of (-)-ulapualide A, a novel tris-oxazole macrolide from marine nudibranchs, based on some biosynthesis speculation

Author keywords

[No Author keywords available]

Indexed keywords

BIOSYNTHETIC ORIGIN; COMETABOLITES; OXAZOLE RINGS; PROTECTING GROUPS;

EID: 41549092718     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b801036f     Document Type: Article
Times cited : (30)

References (67)
  • 31
    • 0000814409 scopus 로고
    • The oxazole methyl bromide 14 was obtained from (S)-tert-butyl 2-(2-(benzyloxy)acetamido)hydroxypropanoate by cyclisation and oxidation using DAST, bromotrichloromethane and DBU, followed by manipulation of the functionality in the resulting tert-butyl 2-(benzyloxy)methyl)oxazole-4- carboxylate; cf. -2392
    • H. C. Brown R. S. Randad K. S. Bhat M. Zaidlewicz U. S. Racherla J. Am. Chem. Soc. 1990 112 2389 2392
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2389
    • Brown, H.C.1    Randad, R.S.2    Bhat, K.S.3    Zaidlewicz, M.4    Racherla, U.S.5
  • 33
    • 0020614964 scopus 로고
    • We thank Professor A. J. Blake of this department for this X-ray analysis, which has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 639019 -2294
    • Y. Nagao S. Yamada E. Fujita Tetrahedron Lett. 1983 24 2291 2294
    • (1983) Tetrahedron Lett. , vol.24 , pp. 2291
    • Nagao, Y.1    Yamada, S.2    Fujita, E.3
  • 38
    • 41549120533 scopus 로고    scopus 로고
    • University of Nottingham
    • Alternative approaches were developed simultaneously; see: J. Kempson, PhD Thesis, University of Nottingham, 2000
    • (2000)
    • Kempson, J.1
  • 64
    • 12044258245 scopus 로고
    • For a review on some incorrectly assigned structures of natural products, see: -4398
    • L. A. Carpino J. Am. Chem. Soc. 1993 115 4397 4398
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 4397
    • Carpino, L.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.