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Volumn 38, Issue 22, 1997, Pages 3911-3914

The highly diastereoselective palladium-catalyzed cyclizations. Stereoselective syntheses of cis and trans-disubstituted hydroxycyclopentanes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTANE DERIVATIVE; HYDROXYCYCLOPENTANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030979211     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00777-6     Document Type: Article
Times cited : (18)

References (24)
  • 12
    • 0343906388 scopus 로고    scopus 로고
    • note
    • Stereochemical assignments were made by bromolactonization after hydrolysis of the bicyclolactone 7a. The hydroxy acid from the isomer 7a provided the 5-membered bromolactone by NBS treatment (DMF, 25°C) in 3 hours while that from 8a remained intact under the same reaction conditions.
  • 19
    • 0001664246 scopus 로고
    • b) Gais, H.-J.; Schmiedl, G.; Ball, W. A.; Bund, J.; Hellmann, G.; Erdelmeier, I. Tetrahedron Lett. 1988, 29, 1773. Rehwinkel, H.; Skupsch, J.; Vorbrüggen, H. Tetrahedron Lett. 1988, 29, 1775.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 1775
    • Rehwinkel, H.1    Skupsch, J.2    Vorbrüggen, H.3
  • 23
    • 0343470466 scopus 로고
    • We thank Dr. Rehwinkel of Research Laboratories, Schering AG, Berlin for kindly providing spectral data of the final product 14. a) Benna, B.; Dahl, H.; Vorbrüggen, H. Synthesis 1986, 41.
    • (1986) Synthesis , pp. 41
    • Benna, B.1    Dahl, H.2    Vorbrüggen, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.