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Volumn 350, Issue 2, 2008, Pages 303-314

Palladium-catalyzed diastereoselective and enantioselective allylic alkylations of ketone enolates

Author keywords

Allyl complexes; Asymmetric synthesis; Lithium; Nucleophilic additions; Stereoselectivity

Indexed keywords


EID: 38849135960     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700409     Document Type: Article
Times cited : (50)

References (79)
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    • For the preparation of lib, see: S. Hillebrand, J. Bruckmann, C. Krüger, M. W. Haenel, Tetrahedron Lett. 1995, 36, 75. All other ligands shown in Scheme 4 are commercially available and were purchased.
    • For the preparation of lib, see: S. Hillebrand, J. Bruckmann, C. Krüger, M. W. Haenel, Tetrahedron Lett. 1995, 36, 75. All other ligands shown in Scheme 4 are commercially available and were purchased.
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    • Cf: a) S. Ramdeehul, P. Dierkes, R. Aguado, P. C. J. Kamer, P. W. N. M. van Leeuwen, J. A. Osborn, Angew. Chem. 1998, 110, 3302;
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    • The lithium salt might also influence the aggragation of the metal catalyst
    • Angew. Chem. Int. Ed. Engl. 1988, 27, 1624. The lithium salt might also influence the aggragation of the metal catalyst,
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.