標(biāo)題: Titlebook: ; [打印本頁(yè)] 作者: Aggrief 時(shí)間: 2025-3-21 20:04
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery影響因子(影響力)
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery影響因子(影響力)學(xué)科排名
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery被引頻次
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery被引頻次學(xué)科排名
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery年度引用
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery年度引用學(xué)科排名
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery讀者反饋
書(shū)目名稱(chēng)Green Chemistry in Drug Discovery讀者反饋學(xué)科排名
作者: 決定性 時(shí)間: 2025-3-21 21:30
J. Syka,R. Druga,J. Popelá?,B. Kalinováke compounds for further biological evaluation. In addition, the power of cascade strategies is also demonstrated in the pilot plant-scale synthesis of highly valued, structurally complex drugs and drug candidates.作者: 激怒 時(shí)間: 2025-3-22 00:41 作者: 袖章 時(shí)間: 2025-3-22 06:37
https://doi.org/10.1007/978-3-322-92118-5ugh are far less established in terms of their broad scope and utility. The current chapter focuses on emerging developments in the use of non-precious metals in catalysis with potential applications in both research and development.作者: 偽證 時(shí)間: 2025-3-22 12:15 作者: 鑲嵌細(xì)工 時(shí)間: 2025-3-22 15:12
Designing Efficient Cascade Reactions in Drug Discoveryke compounds for further biological evaluation. In addition, the power of cascade strategies is also demonstrated in the pilot plant-scale synthesis of highly valued, structurally complex drugs and drug candidates.作者: 鑲嵌細(xì)工 時(shí)間: 2025-3-22 20:46
C–H Activation with Photoredox Catalysis been shown to be effective in C–H activation in its own right, providing access to a complementary?set of reactions to those exhibited by other metal complexes. Here, we summarize some of the key advancements in the use of photoredox catalysis for the C–H activation of organic substrates.作者: 大溝 時(shí)間: 2025-3-23 00:38 作者: 逗它小傻瓜 時(shí)間: 2025-3-23 05:26 作者: Notify 時(shí)間: 2025-3-23 08:33
,Grundlagen des neuromuskul?ren Monitorings,he most fundamental groups of organic reactions in a responsible and environmentally friendly manner. Utilization of now available methods of nanotechnology and non-traditional sources of energy paves the way for the further implementation of the principles of “green” chemistry for industrial Friedel-Crafts reactions.作者: musicologist 時(shí)間: 2025-3-23 12:00
Neuronal-glial Cell Interrelationshipsle drugs and drug candidates. The discussion will restrict itself to situations where protection has been achieved using a protecting group. In addition, in order to assist with their reduction to practice, we provide example procedures where these methodologies have been used.作者: commensurate 時(shí)間: 2025-3-23 16:42
Regelungstechnische Anwendungen von KNN,s showcased. Attention is focused on areas such as hazardous transformations, multistep synthesis, photochemistry, electrochemistry, and organocatalysis. The scope of the chapter is also broadened to techniques used for monitoring flow processes and the incorporation of flow chemistry into the undergraduate teaching laboratory.作者: 嬉耍 時(shí)間: 2025-3-23 20:40 作者: ingestion 時(shí)間: 2025-3-23 23:19
Klaus-Peter Wiedmann,Frank Bucklerbeen developed for targets including fatty acid amide hydrolase, monoamine oxidase B, and glycogen synthase kinase 3β. The versatility of these technologies has also facilitated high-throughput discovery of fluorine-18-labeled radiotracers.作者: 裂隙 時(shí)間: 2025-3-24 02:20 作者: plasma 時(shí)間: 2025-3-24 08:04 作者: 1分開(kāi) 時(shí)間: 2025-3-24 10:57
Direct Nucleophilic Substitution of Alcohols by Br?nsted or Lewis Acids Activation: An Update Br?nsted acid. With particular focus on the literature since 2011, an initial overview of carbenium ion reactivity is provided followed by a survey of displacement reactions grouped by the nature of the nucleophile. Finally, advances in both diastereoselective and enantioselective variants of the reaction are discussed.作者: 星星 時(shí)間: 2025-3-24 15:57
Friedel-Crafts Reactionshe most fundamental groups of organic reactions in a responsible and environmentally friendly manner. Utilization of now available methods of nanotechnology and non-traditional sources of energy paves the way for the further implementation of the principles of “green” chemistry for industrial Friedel-Crafts reactions.作者: Postulate 時(shí)間: 2025-3-24 19:29 作者: hereditary 時(shí)間: 2025-3-25 02:33 作者: 暫停,間歇 時(shí)間: 2025-3-25 04:22
https://doi.org/10.1007/978-3-642-13477-7cussed. We will group catalytic methods by which functional moieties (e.g., alcohol, aldehyde, nitrile, azide, and acid homologs) are used as starting materials for the reaction. We hope to inform the reader of the broad scope of “green” amide bond-forming reactions which can be used in lieu of canonical peptide coupling reagents.作者: 指令 時(shí)間: 2025-3-25 08:40
Rhabdomyolyse und Myoglobinurie,this chapter, recent applications of the Mitsunobu reaction in medicinal and process chemistry will be described, while recent modifications of the Mitsunobu reaction will be addressed in the second section with a focus on “greener” methodologies.作者: 延期 時(shí)間: 2025-3-25 13:09 作者: 落葉劑 時(shí)間: 2025-3-25 16:45
Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modificationsthis chapter, recent applications of the Mitsunobu reaction in medicinal and process chemistry will be described, while recent modifications of the Mitsunobu reaction will be addressed in the second section with a focus on “greener” methodologies.作者: 薄荷醇 時(shí)間: 2025-3-25 21:37
Samuel H. Barondes,Steven D. Rosen organic molecules. Recent advances in the field have focused on the development of new catalytic systems that are both highly reactive and predictably selective. These recently developed C–H functionalization methods have the potential to not only streamline synthesis but also allow access to novel作者: famine 時(shí)間: 2025-3-26 01:33 作者: deceive 時(shí)間: 2025-3-26 04:37
Green Chemistry in Drug Discovery978-1-0716-1579-9Series ISSN 1557-2153 Series E-ISSN 1940-6053 作者: 冷峻 時(shí)間: 2025-3-26 10:47 作者: 著名 時(shí)間: 2025-3-26 12:49
,Neuronale Modelle für Strategielernen,g of pharmaceutical compounds. This review describes recent progress in the development of ene-reductases, oxygenases, and enzymes for amide and amine synthesis, with a focus on academic and industrial collaborations.作者: cocoon 時(shí)間: 2025-3-26 19:09 作者: AMPLE 時(shí)間: 2025-3-26 22:45 作者: languor 時(shí)間: 2025-3-27 03:39 作者: 令人悲傷 時(shí)間: 2025-3-27 06:48 作者: Rinne-Test 時(shí)間: 2025-3-27 13:10
Neuromuscular Urgencies and Emergenciesof non-aromatic heterocycles, one-ring aromatic heterocycles, and their condensed analogs. Due to the great variety of and high interest in these compounds, the work focuses on providing representative examples of the preparation of the target compounds.作者: 流利圓滑 時(shí)間: 2025-3-27 16:20 作者: KEGEL 時(shí)間: 2025-3-27 18:23 作者: 增長(zhǎng) 時(shí)間: 2025-3-28 00:07 作者: DAUNT 時(shí)間: 2025-3-28 02:33 作者: 競(jìng)選運(yùn)動(dòng) 時(shí)間: 2025-3-28 09:47 作者: 合乎習(xí)俗 時(shí)間: 2025-3-28 14:13 作者: 喊叫 時(shí)間: 2025-3-28 15:36
Oscillations and Synchrony in Attentionent of lead matter in drug discovery. Given the numerous advantages that these processes possess not only from the ability to generate large numbers of diverse compounds but also from a sustainability perspective, it is somewhat surprising that MCRs have not enjoyed such a widespread application in 作者: enterprise 時(shí)間: 2025-3-28 21:36 作者: 潰爛 時(shí)間: 2025-3-29 00:17
Rebecca J. Henderson,James R. Connormpounds. While C–H bonds have traditionally been considered inert, methods for activation of C–H bonds with transition metals have become an effective means to selectively functionalize organic substrates based upon careful reaction design. Recently, the use of visible light photoredox catalysis has作者: 有法律效應(yīng) 時(shí)間: 2025-3-29 04:17
Neuronal-glial Cell Interrelationshipsrs. Herein we review in situ protecting group strategies that have been applied, or have the potential to be applied, to the synthesis of small molecule drugs and drug candidates. The discussion will restrict itself to situations where protection has been achieved using a protecting group. In additi作者: Celiac-Plexus 時(shí)間: 2025-3-29 11:00 作者: Ornament 時(shí)間: 2025-3-29 14:28 作者: Phonophobia 時(shí)間: 2025-3-29 18:28 作者: 閑聊 時(shí)間: 2025-3-29 20:05 作者: Obsequious 時(shí)間: 2025-3-29 23:59 作者: maculated 時(shí)間: 2025-3-30 07:27
Green Synthesis of Common Heterocyclesof non-aromatic heterocycles, one-ring aromatic heterocycles, and their condensed analogs. Due to the great variety of and high interest in these compounds, the work focuses on providing representative examples of the preparation of the target compounds.作者: 誘惑 時(shí)間: 2025-3-30 10:58
Greener Methods for Amide Bond Synthesisst easily accomplished via condensation at high temperatures using amines and carboxylic acids, but peptide coupling agents are pervasively used to form amides under milder conditions. While these coupling agents are robust synthetic reagents, they are generally used in super stoichiometric amounts 作者: 滲入 時(shí)間: 2025-3-30 16:27 作者: 緯度 時(shí)間: 2025-3-30 20:11 作者: 剝皮 時(shí)間: 2025-3-30 23:18 作者: 極肥胖 時(shí)間: 2025-3-31 04:14 作者: pacifist 時(shí)間: 2025-3-31 08:36 作者: dyspareunia 時(shí)間: 2025-3-31 10:38 作者: 老巫婆 時(shí)間: 2025-3-31 13:59
Direct C–H Functionalization Approaches to Pharmaceutically Relevant Molecules This is due to the prevalence of both aromatic moieties and heteroatoms in pharmaceutical, agrochemical, material, and natural products. More traditional and established cross-coupling approaches rely on tactically installed metal-activating groups, and as such, the transformation of these function作者: 感情脆弱 時(shí)間: 2025-3-31 20:06
