Nickel-catalyzed migratory alkyl–alkyl cross-coupling reaction. Issue 38 (18th September 2020)

• Record Type: Journal Article
• Authors: Li, Yangyang; Li, Yuqiang; Peng, Long; Wu, Dong; Zhu, Lei; Yin, Guoyin
• Is Part Of: Chemical science. Volume 11:Issue 38(2020)
• Page Start: 10461
• Page End: 10464
• Publication Date: 2020-09-18
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc03217d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : The selective cross-coupling of activated electrophiles with unactivated ones has been regarded as a challenging task in cross-electrophile couplings. Abstract : The selective cross-coupling of activated electrophiles with unactivated ones has been regarded as a challenging task in cross-electrophile couplings. Herein we describe a migratory cross-coupling strategy, which can overcome this obstacle to access the desired cross-coupling products. Accordingly, a selective migratory cross-coupling of two alkyl electrophiles has been accomplished by nickel catalysis. Remarkably, this alkyl–alkyl cross-coupling reaction provides a platform to prepare 2°–2° carbon–carbon bonds from 1° and 2° carbon coupling partners. Preliminary mechanistic studies suggest that chain-walking occurs at both alkyl halides in this reaction, thus a catalytic cycle with the key step involving two alkylnickel(ii ) species is proposed for this transformation.