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Volumn 65, Issue 12, 2000, Pages 3836-3845

Enantioselective diene cyclization/hydrosilylation catalyzed by optically active palladium bisoxazoline and pyridineoxazoline complexes

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLINE DERIVATIVE; PALLADIUM; PYRIDINE;

EID: 0034674614     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0003192     Document Type: Article
Times cited : (72)

References (123)
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    • For reviews on transition metal-catalyzed carbocyclization, see (a) Ojima, I.; Tzamarioudaki, M.; Li, Z.; Donovan, R. J. Chem. Rev. 1996, 96, 635. (b) Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49. (c) Trost, B. M. Science 1991, 254, 1471. (d) Trost, B. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 259. (e) Trost, B. M.; Krische, M. J. Synlett, 1998, 1.
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    • note
    • The formation of 6 was traced, at least in part, to the presence of trace amounts of water in the solvent and/or borate salt.
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    • note
    • The C-C bond of the olefin must lie in the coordination plane for β-migratory insertion to occur through a concerted four-centered transition state.
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    • note
    • Although bisoxazoline catalyst S,S-4c led to the opposite sense of asymmetric induction relative to bisoxazoline catalysts S,S-4a and R,R-4b, use of catalyst S,S-4c led to formation of only traces (∼6%) of silylated carbocycle.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.