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Volumn 19, Issue 52, 2013, Pages 17698-17701

Enantiospecific, regioselective cross-coupling reactions of secondary allylic boronic esters

Author keywords

allylboronate; cross coupling; stereospecificity; Suzuki Miyaura; synthetic methods

Indexed keywords

ALLYLBORONATE; CROSS-COUPLINGS; STEREOSPECIFICITY; SUZUKI-MIYAURA; SYNTHETIC METHODS;

EID: 84891030906     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201303683     Document Type: Article
Times cited : (67)

References (54)
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    • Springer, Berlin, Szabo proposes an alternative mechanism for highly γ-selective arylations of allylic boronic esters, which involves carbopalladation followed by subsequent elimination of the palladium boronate (see ref.[10h]). The stereospecificity observed here is inconsistent with such a mechanism in our system.
    • U. Kazmaier, Topics in Organic Chemistry 38: Transition Metal Catalysed Enantioselective Allylic Substitution in Organic Synthesis, Springer, Berlin, 2012; Szabo proposes an alternative mechanism for highly γ-selective arylations of allylic boronic esters, which involves carbopalladation followed by subsequent elimination of the palladium boronate (see ref.[10h]). The stereospecificity observed here is inconsistent with such a mechanism in our system.
    • (2012) Topics in Organic Chemistry 38: Transition Metal Catalysed Enantioselective Allylic Substitution in Organic Synthesis
    • Kazmaier, U.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.