Nickel-Catalyzed Reductive Couplings
Topics in Current Chemistry, ISSN: 0340-1022, Vol: 374, Issue: 4, Page: 43
2016
- 288Citations
- 89Captures
- 1Mentions
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations288
- Citation Indexes288
- 288
- CrossRef18
- Captures89
- Readers89
- 89
- Mentions1
- News Mentions1
- 1
Most Recent News
配位子を着せ替え！？クロースカップリング反応
三級アルキルブロミドと種々のアリール求電子剤とのクロスカップリング反応が開発された。ニッケルの配位子を系中で交換させることがC–C結合形成の鍵である。 ニッケル触媒を用いた求電子剤同士のクロスカップリング反応 求電子剤同 […]
Book Chapter Description
The Ni-catalyzed reductive coupling of alkyl/aryl with other electrophiles has evolved to be an important protocol for the construction of C–C bonds. This chapter first emphasizes the recent progress on the Ni-catalyzed alkylation, arylation/vinylation, and acylation of alkyl electrophiles. A brief overview of CO fixation is also addressed. The chemoselectivity between the electrophiles and the reactivity of the alkyl substrates will be detailed on the basis of different Ni-catalyzed conditions and mechanistic perspective. The asymmetric formation of C(sp)–C(sp) bonds arising from activated alkyl halides is next depicted followed by allylic carbonylation. Finally, the coupling of aryl halides with other C(sp)–electrophiles is detailed at the end of this chapter.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84976345139&origin=inward; http://dx.doi.org/10.1007/s41061-016-0042-2; http://www.ncbi.nlm.nih.gov/pubmed/27573395; http://link.springer.com/10.1007/s41061-016-0042-2; https://dx.doi.org/10.1007/s41061-016-0042-2; https://link.springer.com/article/10.1007/s41061-016-0042-2
Springer Nature
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know