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Volumn 23, Issue 8, 1982, Pages 807-810

Stereoselective reactions of chiral enolates. Application to the synthesis of (+)-prelog-djerassi lactonic acid.

Author keywords

[No Author keywords available]

Indexed keywords

DRUG ANALYSIS; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; PRELOG DJERASSI LACTONE; STEREOCHEMISTRY; THEORETICAL STUDY;

EID: 0020064919     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)86954-3     Document Type: Article
Times cited : (95)

References (20)
  • 1
    • 84981833185 scopus 로고
    • Stoffwechselprodukte von Actinomyceten. 5. Mitteilung. �ber das Lacton der ?-Hydroxy-?, ??, ?-trimethyl-pimelins�ure, ein Abbauprodukt von Narbomycin, Pikromycin und Methymycin
    • (1956) Helvetica Chimica Acta , vol.39 , pp. 1785-1790
    • Anliker1    Dvornik2    Gubler3    Heusser4    Prelog5
  • 9
    • 84918367768 scopus 로고    scopus 로고
    • Evans, D. A.; Ennis, M. D.; Mahre, D. J. J. Am. Chem. Soc. in press.
  • 11
    • 84918367767 scopus 로고    scopus 로고
    • Diastereomer analysis was carried out on a 5880A Hewlett-Packard gas chromatograph employing 30 × 0.32 M WCOT columns (Carbowax 20 M, Methyl Silicone SE-54).
  • 12
    • 84918367766 scopus 로고    scopus 로고
    • Chromatographic resolutions were carried out with Merck LoBar Silica Gel columns.
  • 16
    • 84918367765 scopus 로고    scopus 로고
    • 4 in 8b may be resolved.
  • 17
    • 84918367764 scopus 로고    scopus 로고
    • Evans, D.A.; Bartroli, J.; Godel, T. Tetrahedron Lett. in press.
  • 19
    • 84918367763 scopus 로고    scopus 로고
    • 2e
  • 20
    • 84918367762 scopus 로고    scopus 로고
    • All compounds prepared during the course of this study afforded consistent elemental analyses and spectral data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.