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Volumn 67, Issue 5, 2011, Pages 927-935

Anti-Aldol reactions of chiral alcohol-substituted vinylogous urethanes and the synthesis of (-)-prelactone B

Author keywords

( ) Prelactone B; anti Aldol reaction; Vinylogous urethane lactones; Vinylogous urethanes

Indexed keywords

1 (HYDROXYDIPHENYLMETHYL) 7,7 DIMETHYLBICYCLO[2.2.1]HEPTAN 2 OL; ALCOHOL; BICYCLO COMPOUND; LACTONE DERIVATIVE; NATURAL PRODUCT; PRELACTONE B; UNCLASSIFIED DRUG; URETHAN DERIVATIVE; VINYL DERIVATIVE;

EID: 78651353566     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.12.009     Document Type: Article
Times cited : (6)

References (51)
  • 1
  • 8
    • 78651362472 scopus 로고
    • Ph.D. Thesis, University of Rochester, Rochester, New York, NY
    • Von Langen, D.J. Ph.D. Thesis, University of Rochester, Rochester, New York, NY, 1991.
    • (1991)
    • Von Langen, D.J.1
  • 10
    • 0000059122 scopus 로고
    • Chiral alcohols 2a-d were purchased commercially from Aldrich®, synthesis of 2e-m see: W. Oppolzer, R. Radinov, and N. Rumen Tetrahedron Lett. 29 1988 5645 5648
    • (1988) Tetrahedron Lett. , vol.29 , pp. 5645-5648
    • Oppolzer, W.1    Radinov, R.2    Rumen, N.3
  • 14
    • 78651359647 scopus 로고    scopus 로고
    • Ibid., 1489-1502
    • Ibid., 14891502
  • 18
    • 78651347621 scopus 로고    scopus 로고
    • CCDC 801188 and CCDC 801189 contain the supplementary crystallographic data for 4g and 4o. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • CCDC 801188 and CCDC 801189 contain the supplementary crystallographic data for 4g and 4o. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 19
    • 78651353597 scopus 로고    scopus 로고
    • The retention time of the two enantiomers were 31.5 min and 35.2 min, respectively, under a 0.5 mL/min flow rate, using n-hexane/ethanol 94/6 as the eluent. A 31.5 min peak was the major enantiomer
    • The retention time of the two enantiomers were 31.5 min and 35.2 min, respectively, under a 0.5 mL/min flow rate, using n-hexane/ethanol 94/6 as the eluent. A 31.5 min peak was the major enantiomer.
  • 20
    • 78651353434 scopus 로고    scopus 로고
    • Isolation of prelactones see:
    • Isolation of prelactones see:
  • 35
    • 78651355839 scopus 로고    scopus 로고
    • 1 see:
    • 1 see:
  • 38
    • 78651369931 scopus 로고    scopus 로고
    • 1 see:
    • 1 see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.