无力向前 发表于 2025-3-21 18:43:19
书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis影响因子(影响力)<br> http://impactfactor.cn/if/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis影响因子(影响力)学科排名<br> http://impactfactor.cn/ifr/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis网络公开度<br> http://impactfactor.cn/at/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis网络公开度学科排名<br> http://impactfactor.cn/atr/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis被引频次<br> http://impactfactor.cn/tc/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis被引频次学科排名<br> http://impactfactor.cn/tcr/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis年度引用<br> http://impactfactor.cn/ii/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis年度引用学科排名<br> http://impactfactor.cn/iir/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis读者反馈<br> http://impactfactor.cn/5y/?ISSN=BK0660007<br><br> <br><br>书目名称N-Heterocyclic Carbenes in Transition Metal Catalysis读者反馈学科排名<br> http://impactfactor.cn/5yr/?ISSN=BK0660007<br><br> <br><br>Jocose 发表于 2025-3-21 22:16:09
https://doi.org/10.1007/978-3-540-36930-1Heterocyclic Chemistry; Medicinal Chemistry; Organometallic Chemistry; Oxidation; catalysisComplement 发表于 2025-3-22 01:23:32
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,N-Heterocyclic Carbenes in Catalysis—An Introduction,N-Heterocyclic carbene (NHC) has become a major ligand class and has proven to be more than just a “phosphine mimic”. Some important features like electronic and steric properties are discussed and typical examples of NHC are given herein.Frisky 发表于 2025-3-22 11:54:38
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978-3-642-07197-3Springer-Verlag Berlin Heidelberg 2007赏钱 发表于 2025-3-22 21:22:33
N-Heterocyclic Carbenes in Transition Metal Catalysis978-3-540-36930-1Series ISSN 1436-6002 Series E-ISSN 1616-8534修饰语 发表于 2025-3-23 03:27:29
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Routes to N-Heterocyclic Carbene Complexes,; (3) use of preformed, isolated free carbenes; (4) deprotonation of an azolium salt with a base; (5) transmetallation from an Ag — NHC complex prepared from direct reaction of an imidazolium precursor and Ag2O; and (6) oxidative addition via activation of the C2 — X (X = Me, halogen, H) of an imidazolium cation.