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Volumn 39, Issue 1, 2000, Pages 209-213

Enantioselective total synthesis of epothilone A using multifunctional asymmetric catalyses

Author keywords

Asymmetric catalysis; Epothilones; Total synthesis

Indexed keywords

EPOTHILONE A; EPOTHILONE B;

EID: 0034598534     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(20000103)39:1<209::AID-ANIE209>3.0.CO;2-F     Document Type: Article
Times cited : (95)

References (45)
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    • For an enantioselective total synthesis of epothilone A using antibody catalysis, see reference [2k]
    • For an enantioselective total synthesis of epothilone A using antibody catalysis, see reference [2k].
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    • The absolute configuration was determined by Mosher's method; see J. A. Dale, H. S. Mosher, J. Am. Chem. Soc. 1973, 95, 512-519. The enantiomeric excess was determined by HPLC analysis using DAICEL CHIRALPAK AD (2-propanol/hexane 1/100).
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    • note
    • [5] it is possible to prepare syn- and anti-aldol from cis- and trans-enones, respectively, with excellent ee values (Table 1).
  • 43
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    • note
    • a (10.2 Hz). (formula presented)
  • 44
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    • note
    • [8] and the enantiomeric excesses were determined by HPLC analysis using DAI-CEL, CHIRALPAK AD (2-propanol/ hexane 1/100). The relative configurations were determined by transforming 24 into 32 and 25 into 33 (cyclization of 27 and 34, respectively), and analyzing their NOEs. (formula presented) (formula presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.