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Volumn , Issue 11, 2011, Pages 1555-1558

Synthetic approaches to the bottom half fragment for bryostatin 11

Author keywords

asymmetric aldol; bottom half fragment; bryostatin 11; Saksena Evans reduction; thioketalization lactonization

Indexed keywords

BRYOSTATIN; BRYOSTATIN 11; UNCLASSIFIED DRUG;

EID: 79959376111     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1260784     Document Type: Article
Times cited : (3)

References (38)
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    • For recent reviews on bryostatin chemistry and biology, see:, Mutter R, Wills M, Bioorg. Med. Chem. 2000 8 1841
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    • Mutter, R.1    Wills, M.2
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    • references cited therein
    • Pettit G R., J. Nat. Prod. 1996 59 812; and references cited therein
    • (1996) J. Nat. Prod. , vol.59 , pp. 812
    • Pettit, G.R.1
  • 31
    • 0028094650 scopus 로고
    • The constructions of similar aldehydes via anti -selective allylation have been reported by other groups. See
    • The constructions of similar aldehydes via anti -selective allylation have been reported by other groups. See:, De Brabander J, Vandewalle M, Synthesis 1994 855
    • (1994) Synthesis , pp. 855
    • De Brabander, J.1    Vandewalle, M.2
  • 36
    • 3042697283 scopus 로고    scopus 로고
    • 2 as a Lewis acid provided a 5:1 selectivity ratio. See
    • 2 as a Lewis acid provided a 5:1 selectivity ratio. See:, Voight E A., Roethle P A., Burke S D., J. Org. Chem. 2004 69 4534
    • (2004) J. Org. Chem. , vol.69 , pp. 4534
    • Voight, E.A.1    Roethle, P.A.2    Burke, S.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.