代表 发表于 2025-3-21 19:19:55
书目名称Application of Transition Metal Catalysts in Organic Synthesis影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0159190<br><br> <br><br>书目名称Application of Transition Metal Catalysts in Organic Synthesis读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0159190<br><br> <br><br>dearth 发表于 2025-3-21 22:29:57
http://reply.papertrans.cn/16/1592/159190/159190_2.png高度 发表于 2025-3-22 03:04:30
http://reply.papertrans.cn/16/1592/159190/159190_3.pngELATE 发表于 2025-3-22 07:31:47
Springer Desktop Editions in Chemistryhttp://image.papertrans.cn/a/image/159190.jpg发酵 发表于 2025-3-22 12:16:07
http://reply.papertrans.cn/16/1592/159190/159190_5.png现存 发表于 2025-3-22 13:52:51
Nickel- and Palladium-Catalyzed Cross-Coupling Reactions with Organometallic Intermediates,kel compounds, such as dichloro nickel(II) (NiCl.-dppe) and nickel acetylacetonate (Ni(acac).). Somewhat later coupling reactions were carried out with other organometallic compounds unDEr the influence of various nickel and palladium catalysts.FEMUR 发表于 2025-3-22 17:40:55
http://reply.papertrans.cn/16/1592/159190/159190_7.pngFrequency 发表于 2025-3-23 01:11:24
https://doi.org/10.1007/978-3-030-83647-4experimental procedures are given for a number of halides with relatively simple structures that are either not (yet) commercially available, very expensive or have a limited stability. The procedures are modifications or optimizations of published ones. A number of substituted aryl halides can be pimmunity 发表于 2025-3-23 01:47:03
Adheesh Shah,Vinayak A. Modi,M. Boopathiries such reactions are facilitated by electron-withdrawing groups. In the chemistry of aromatic compounds the analogous reactions are called S.Ar substitutions. Although the processes are considerably promoted by electron-withdrawing groups, e. g. N0., in the .- or .-position , they can occurFLING 发表于 2025-3-23 06:36:21
Andrea Bisegna,Roberto Carbone,Silvio Ranisey heating with an alkali iodide in a suitable organic solvent. These reactions, which take place in the absence of any catalyst, proceed to completion thanks to the slight solubility of the alkali chloride or bromide in the applied solvent.