Titlebook: Application of Transition Metal Catalysts in Organic Synthesis; L. Brandsma,H. D. Verkruijsse,S. F. Vasilevsky Book 1999 Springer-Verlag B

代表

書目名稱Application of Transition Metal Catalysts in Organic Synthesis影響因子(影響力)




書目名稱Application of Transition Metal Catalysts in Organic Synthesis影響因子(影響力)學科排名




書目名稱Application of Transition Metal Catalysts in Organic Synthesis網(wǎng)絡(luò)公開度




書目名稱Application of Transition Metal Catalysts in Organic Synthesis網(wǎng)絡(luò)公開度學科排名




書目名稱Application of Transition Metal Catalysts in Organic Synthesis被引頻次




書目名稱Application of Transition Metal Catalysts in Organic Synthesis被引頻次學科排名




書目名稱Application of Transition Metal Catalysts in Organic Synthesis年度引用




書目名稱Application of Transition Metal Catalysts in Organic Synthesis年度引用學科排名




書目名稱Application of Transition Metal Catalysts in Organic Synthesis讀者反饋




書目名稱Application of Transition Metal Catalysts in Organic Synthesis讀者反饋學科排名

dearth

高度

ELATE

Springer Desktop Editions in Chemistryhttp://image.papertrans.cn/a/image/159190.jpg

發(fā)酵

現(xiàn)存

Nickel- and Palladium-Catalyzed Cross-Coupling Reactions with Organometallic Intermediates,kel compounds, such as dichloro [1,2-bis(diphenylphosphino)ethane] 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

Frequency

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 p

immunity

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 [1,4], they can occur

FLING

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.