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Volumn , Issue 6, 1996, Pages 899-911

The use of vicinal twofold Heck reaction products in diastereoselective sequential Michael additions - A convenient access to enantiomerically pure six-ring anellated cispentacin derivatives

Author keywords

Heck reaction; Michael addition, diastereoselective; Palladium catalysis; Amino acids

Indexed keywords


EID: 33748956330     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199619960607     Document Type: Article
Times cited : (40)

References (70)
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    • Lansky, A.1
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    • Voigt, K.1
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    • [9b] D. C. Cole, Tetrahedron 1994, 50, 9517-9582.
    • (1994) Tetrahedron , vol.50 , pp. 9517-9582
    • Cole, D.C.1
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    • [17c] B. H. Kim, Tetrahedron 1993, 49, 293-318.
    • (1993) Tetrahedron , vol.49 , pp. 293-318
    • Kim, B.H.1
  • 64
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    • note
    • Further details of the crystal structure investigations are available from the Fachinformationszentrum Karlsruhe, D-76344 Eggenstein-Leopoldshafen (Germany), on quoting the depository numbers CSD-404994 and -404995, the names of the authors and the journal citation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.