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Volumn 87, Issue 1 SPEC. ISS., 2009, Pages 264-271

Mechanistic investigations of bipyrimidine-promoted palladium-catalyzed allylic acetoxylation of olefins

Author keywords

Allylic C H oxidation; Bipyrimidine; Olefin; P benzoquinone; Palladium catalysis

Indexed keywords

ACETOXYLATION; ALLYL ACETATE; ALLYLBENZENE; ALLYLIC C-H OXIDATION; ALLYLIC OXIDATION; BIPYRIMIDINE; C-H ACTIVATION; CATALYST PRECURSORS; CYCLOHEXENE; DISPROPORTIONATION; MECHANISTIC STUDIES; P-BENZOQUINONE; PALLADIUM CATALYSIS; TERMINAL OLEFINS;

EID: 67650924595     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V08-133     Document Type: Article
Times cited : (59)

References (27)
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    • A small amount of 1-phenylallyl acetate (∼9%) is also formed during the reaction. More detailed mechanistic studies are underway to reconcile this observation with the proposed mechanism.
    • A small amount of 1-phenylallyl acetate (∼9%) is also formed during the reaction. More detailed mechanistic studies are underway to reconcile this observation with the proposed mechanism.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.