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Volumn 5, Issue 4, 2003, Pages 599-602

Toward the synthesis of peloruside A: Fragment synthesis and coupling studies

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMITOTIC AGENT; BORON; CARBON; MACROLIDE; PACLITAXEL; PELORUSIDE A; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; FUSED HETEROCYCLIC RINGS; LACTONE; TUBULIN MODULATOR;

EID: 0001687103     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034035q     Document Type: Article
Times cited : (64)

References (28)
  • 4
    • 0035416117 scopus 로고    scopus 로고
    • For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
    • (2001) Curr. Opin. Chem. Biol. , vol.5 , pp. 424
    • Altmann, K.H.1
  • 5
    • 0035889710 scopus 로고    scopus 로고
    • For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
    • (2001) Drug Discovery Today , vol.6 , pp. 1153
    • He, L.F.1    Orr, G.A.2    Horwitz, S.B.3
  • 6
    • 0034857182 scopus 로고    scopus 로고
    • For recent reviews, see: (a) Altmann, K. H. Curr. Opin. Chem. Biol. 2001, 5, 424. (b) He, L. F.; Orr, G. A.; Horwitz, S. B. Drug Discovery Today 2001, 6, 1153. (c) Stachel, S. J.; Biswas, K.; Danishefsky, S. J. Curr. Pharm. Des. 2001, 7, 1277.
    • (2001) Curr. Pharm. Des. , vol.7 , pp. 1277
    • Stachel, S.J.1    Biswas, K.2    Danishefsky, S.J.3
  • 8
    • 0141602027 scopus 로고    scopus 로고
    • note
    • The absolute configuration of peloruside A has not yet been determined.
  • 14
    • 0141825124 scopus 로고    scopus 로고
    • note
    • The enantiomeric purities of 9 and 14 were determined by chiral HPLC, using the racemic diol as the reference. The absolute configurations were determined by the advanced Mosher method (ref 18 and Supporting Information).
  • 17
    • 0141713775 scopus 로고    scopus 로고
    • note
    • This reaction was accompanied by the formation of the elimination product 2-(4-methoxybenzyloxymethyl)-5-methylfuran.
  • 20
    • 0141490497 scopus 로고    scopus 로고
    • note
    • Ketone 17 was prepared from ethyl (S)-lactate in 62% yield by an identical 3-step sequence to that described in ref 13a for the enantiomeric series.
  • 21
    • 0141490496 scopus 로고    scopus 로고
    • note
    • See the Supporting Information for a proof of stereochemistry of aldol adduct 18.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.