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Volumn 55, Issue 5, 2016, Pages 1849-1853

An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles

Author keywords

alkyl zinc reagents; cross coupling; micelles; palladium precatalysts; surfactants

Indexed keywords

FATTY ACIDS; LIGANDS; MICELLES; PHOSPHORUS COMPOUNDS; SCAFFOLDS; SURFACE ACTIVE AGENTS; ZINC;

EID: 84955667004     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201509341     Document Type: Article
Times cited : (73)

References (44)
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    • The cross-coupling reaction to give 19 c resulted in the deprotection of the azaindole scaffold (removal of the Boc group)
    • The cross-coupling reaction to give 19 c resulted in the deprotection of the azaindole scaffold (removal of the Boc group).
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    • The zincation of these alkyl bromides appears to be slow, as the majority of the alkyl bromide substrate was recovered at the end of the reaction. The product of reduction of the aryl halide was also observed as a result of competitive zinc insertion.
    • The zincation of these alkyl bromides appears to be slow, as the majority of the alkyl bromide substrate was recovered at the end of the reaction. The product of reduction of the aryl halide was also observed as a result of competitive zinc insertion.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.