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Volumn 52, Issue 11, 2011, Pages 1173-1175

Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge batzella sp.

Author keywords

[No Author keywords available]

Indexed keywords

ARABINOSE DERIVATIVE; BATZELLASIDE B; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79751538299     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.01.018     Document Type: Article
Times cited : (12)

References (21)
  • 5
    • 79751530580 scopus 로고    scopus 로고
    • On the basis of the coincidence spectral data and the mechanistic sequence identical to the literature procedure employing D-antipode of 1, it is reasonable to assume that 3 would have the (R)-configuration at the newly formed stereocenter, see Ref. 3a.
    • On the basis of the coincidence spectral data and the mechanistic sequence identical to the literature procedure employing D-antipode of 1, it is reasonable to assume that 3 would have the (R)-configuration at the newly formed stereocenter, see Ref. 3a.
  • 10
    • 79751528517 scopus 로고    scopus 로고
    • 1H NMR spectral data, it is reasonable to assume that 6 was formed as a single diastereomer.
    • 1H NMR spectral data, it is reasonable to assume that 6 was formed as a single diastereomer.
  • 16
    • 79751524590 scopus 로고    scopus 로고
    • 3 at 0.7 M prior to use.
    • 3 at 0.7 M prior to use.
  • 17
    • 79751534224 scopus 로고    scopus 로고
    • The observed optical rotation of 14β ([α]25 +9.3 (c 0.5, MeOH)) close to that for the natural product (lit. [α]D25 +10 (c 0.5, MeOH), see Ref. 1) indicated their structural and stereochemical identity.
    • The observed optical rotation of 14β ([ α ] D 25 +9.3 (c 0.5, MeOH)) close to that for the natural product (lit. [ α ] D 25 +10 (c 0.5, MeOH), see Ref. 1) indicated their structural and stereochemical identity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.