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Volumn 14, Issue 2, 2012, Pages 564-567

Total synthesis of seco-plakortolide e and (-)-ent-plakortolide I: Absolute configurational revision of natural plakortolide i

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; DIOXANE DERIVATIVE; DRUG DERIVATIVE; FUSED HETEROCYCLIC RINGS; GAMMA BUTYROLACTONE; PEROXIDE; PLAKORTOLIDE E; PLAKORTOLIDE I;

EID: 84856094572     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol203185f     Document Type: Article
Times cited : (23)

References (30)
  • 13
    • 84856111477 scopus 로고    scopus 로고
    • We recently applied this concept to the synthesis of a fragment of amphidinolide X
    • We recently applied this concept to the synthesis of a fragment of amphidinolide X: Doan, H. D.; Gallon, J.; Piou, A.; Vatèle, J.-M. Synlett 2011, 983-985
    • (2011) Synlett , pp. 983-985
    • Doan, H.D.1    Gallon, J.2    Piou, A.3    Vatèle, J.-M.4
  • 17
    • 84856111478 scopus 로고    scopus 로고
    • Barnych, B.; Vatèle, J.-M. Unpublished results
    • Barnych, B.; Vatèle, J.-M. Unpublished results.
  • 19
    • 0007858182 scopus 로고
    • The use of Mg Rieke in place of Mg turnings minimized the Wurtz coupling reaction. For the preparation of Mg Rieke, see: Rieke, R. D.; Bates, S. E.; Hudnall, P. M.; Poindexter, G. S. Org. Synth. 1988, 6, 845-851
    • (1988) Org. Synth. , vol.6 , pp. 845-851
    • Rieke, R.D.1    Bates, S.E.2    Hudnall, P.M.3    Poindexter, G.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.