作者: 正式演說 時(shí)間: 2025-3-21 20:51 作者: 翻布尋找 時(shí)間: 2025-3-22 02:49
Recent Advances in Cross-Coupling Reactions with Alkyl Halidesreported. This chapter classifies the recently reported cross-coupling reactions of these alkyl electrophiles, grouping the reactions by organometallic reagent. Introductions to representative synthetic examples are given.作者: 文藝 時(shí)間: 2025-3-22 08:29 作者: 駁船 時(shí)間: 2025-3-22 12:33 作者: inhumane 時(shí)間: 2025-3-22 15:24 作者: 討好女人 時(shí)間: 2025-3-22 19:14 作者: 高歌 時(shí)間: 2025-3-22 23:27
https://doi.org/10.1007/978-3-642-39360-0cross-coupling—underscoring the versatility, effectiveness, functional group tolerance, and mild reaction conditions of the cross-coupling methods. Due to these advantages, palladium-catalyzed cross-coupling reactions are being utilized in the industrial production of pharmaceuticals.作者: MITE 時(shí)間: 2025-3-23 01:34 作者: 未開化 時(shí)間: 2025-3-23 05:50
Pharmaceuticalscross-coupling—underscoring the versatility, effectiveness, functional group tolerance, and mild reaction conditions of the cross-coupling methods. Due to these advantages, palladium-catalyzed cross-coupling reactions are being utilized in the industrial production of pharmaceuticals.作者: 正常 時(shí)間: 2025-3-23 13:37
Liquid Crystalsr new liquid crystalline molecules with novel physical properties. Moreover, the organic molecules synthesized with the cross-coupling reactions may be used in new areas such as organic electroluminescence (EL) and thin film transistors (TFT).作者: CREEK 時(shí)間: 2025-3-23 14:47 作者: 裝飾 時(shí)間: 2025-3-23 20:22 作者: Recess 時(shí)間: 2025-3-23 23:23 作者: malign 時(shí)間: 2025-3-24 03:07 作者: STIT 時(shí)間: 2025-3-24 07:47
Lecture Notes in Computer Scienceds, and the environmental benignness of wastes. In natural product syntheses, the cross-couplings as carbon–carbon bond-forming reactions have been widely utilized for the construction of fragments as the key steps in the total syntheses.作者: gene-therapy 時(shí)間: 2025-3-24 12:12
https://doi.org/10.1007/978-3-642-39360-0ive compounds are of both academic and industrial importance. Drug candidates can be prepared from easily available substrates in a few steps through cross-coupling—underscoring the versatility, effectiveness, functional group tolerance, and mild reaction conditions of the cross-coupling methods. Du作者: 惰性氣體 時(shí)間: 2025-3-24 16:34 作者: 無力更進(jìn) 時(shí)間: 2025-3-24 21:35 作者: 圖畫文字 時(shí)間: 2025-3-24 23:37
https://doi.org/10.1007/978-3-642-32368-3Conjugate Polymers; Cross-coupling Reactions with Alkyl Halides; Cross-coupling Reactions with Aryl Ch作者: 莎草 時(shí)間: 2025-3-25 05:24 作者: 銼屑 時(shí)間: 2025-3-25 10:51 作者: Bone-Scan 時(shí)間: 2025-3-25 11:40
Lecture Notes in Computer ScienceIn the past 10?years, the cross-coupling reactions of the relatively unreactive electrophilic aryl chlorides, -tosylates, and -mesylates have been extensively investigated. Strategies to promote oxidative addition toward inert chemical bonds have included the use of bulky, electron-rich ligands.作者: condone 時(shí)間: 2025-3-25 16:07
Conjugated PolymersThe synthesis of .-conjugated polymers by cross-coupling-based polymerization is a practical method that has been widely employed. The obtained polymers have received considerable attention owing to their interesting properties that have applications as electrochemically conductive materials.作者: micturition 時(shí)間: 2025-3-25 20:26
Recent Advances in Cross-Coupling Reactions with Aryl Chlorides, Tosylates, and MesylatesIn the past 10?years, the cross-coupling reactions of the relatively unreactive electrophilic aryl chlorides, -tosylates, and -mesylates have been extensively investigated. Strategies to promote oxidative addition toward inert chemical bonds have included the use of bulky, electron-rich ligands.作者: 歡騰 時(shí)間: 2025-3-26 00:54 作者: 多樣 時(shí)間: 2025-3-26 07:26
Yasushi NishiharaThe topic of this volume was the subject of the Nobel Prize for Chemistry in 2010.Each chapter is written for students by an expert in the field.Provides a useful reference for students and teachers o作者: HAWK 時(shí)間: 2025-3-26 11:19 作者: defile 時(shí)間: 2025-3-26 16:34 作者: oncologist 時(shí)間: 2025-3-26 19:07 作者: 無意 時(shí)間: 2025-3-27 00:35 作者: 主動 時(shí)間: 2025-3-27 03:56
Erratum to: A Historic Overview of the Metal-Catalyzed Cross-Coupling Reactions,作者: 卵石 時(shí)間: 2025-3-27 09:09
A Historic Overview of the Metal-Catalyzed Cross-Coupling Reactionsse of transition-metal-catalyzed cross-coupling reactions of organic electrophiles with organometallic nucleophiles started with the discovery of Kumada–Tamao–Corriu coupling in 1972—the reaction of organic halides and organomagnesium compounds under nickel catalysis. Combining fragments with a seri作者: 盲信者 時(shí)間: 2025-3-27 09:46 作者: chronology 時(shí)間: 2025-3-27 13:45
Natural Product Synthesisds, and the environmental benignness of wastes. In natural product syntheses, the cross-couplings as carbon–carbon bond-forming reactions have been widely utilized for the construction of fragments as the key steps in the total syntheses.作者: 厚臉皮 時(shí)間: 2025-3-27 18:52 作者: 類似思想 時(shí)間: 2025-3-28 01:50
Liquid Crystalsh underway in various fields exploring other uses. The carbon–carbon bond-forming cross-coupling reactions can provide innovative synthetic methods for new liquid crystalline molecules with novel physical properties. Moreover, the organic molecules synthesized with the cross-coupling reactions may b作者: 梯田 時(shí)間: 2025-3-28 05:57 作者: 神圣將軍 時(shí)間: 2025-3-28 09:25
9樓作者: euphoria 時(shí)間: 2025-3-28 11:17
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10樓作者: 我不明白 時(shí)間: 2025-3-28 21:43
10樓作者: 態(tài)度暖昧 時(shí)間: 2025-3-28 23:26
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