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Volumn 48, Issue 17, 2009, Pages 3146-3149

Palladium-catalyzed oxidative intermolecular difunctionalization of terminal alkenes with organostannanes and molecular oxygen

Author keywords

[No Author keywords available]

Indexed keywords

CATIONIC PALLADIUM COMPLEXES; DIFUNCTIONALIZATION; DIMETHYLACETAMIDE; HYDRIDE ELIMINATION; NONCONJUGATED; ORGANOSTANNANES; RELATIVE RATES; TERMINAL ALKENES; TERMINAL DOUBLE BONDS; TRANSMETALATION;

EID: 70349769744     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200900218     Document Type: Article
Times cited : (162)

References (52)
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    • The hydroarylation product is thought to be formed from a palladium hydride generated from the Heck reaction. However, in some cases in Table 1, the yield of the hydroarylation product is greater than that of the Heck product. The additional palladium hydride may be formed by transmetalation of an n-butyl group from PhSnBu3, followed by ß-hydride elimination
    • 3, followed by ß-hydride elimination.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.