標題: Titlebook: Anthracycline Chemistry and Biology I; Biological Occurence Karsten Krohn Book 2008 Springer-Verlag Berlin Heidelberg 2008 Base.Chemical sy [打印本頁] 作者: obdurate 時間: 2025-3-21 16:52
書目名稱Anthracycline Chemistry and Biology I影響因子(影響力)
書目名稱Anthracycline Chemistry and Biology I影響因子(影響力)學科排名
書目名稱Anthracycline Chemistry and Biology I網(wǎng)絡(luò)公開度
書目名稱Anthracycline Chemistry and Biology I網(wǎng)絡(luò)公開度學科排名
書目名稱Anthracycline Chemistry and Biology I被引頻次
書目名稱Anthracycline Chemistry and Biology I被引頻次學科排名
書目名稱Anthracycline Chemistry and Biology I年度引用
書目名稱Anthracycline Chemistry and Biology I年度引用學科排名
書目名稱Anthracycline Chemistry and Biology I讀者反饋
書目名稱Anthracycline Chemistry and Biology I讀者反饋學科排名
作者: Palate 時間: 2025-3-21 23:39 作者: Gourmet 時間: 2025-3-22 01:48 作者: 燒烤 時間: 2025-3-22 07:09 作者: 中世紀 時間: 2025-3-22 08:53
Combinatorial Synthesis of Linearly Condensed Polycyclic Compounds, Including Anthracyclinones, ThroAlder additions with large reactivity difference betweenthe addition of the first equivalent (..) andthe second equivalent (..) of dienophile. Thisallows one to prepare, through parallel synthesis, a?large number of linearly condensed polycyclicsystems containing three annulated six-membered rings, 作者: Glucose 時間: 2025-3-22 13:18 作者: 巡回 時間: 2025-3-22 18:43
Synthesis of the Sugar Moietiestructure. Modification or switch of the saccharidemoiety became an important line of new drug discovery and study of their mechanism of action. Naturalglycons (sugar moieties) of the anthracycline antibiotics belong to the 2,6-dideoxypyranose familyand their principal representative, daunosamine, is作者: mendacity 時間: 2025-3-22 21:44 作者: vanquish 時間: 2025-3-23 03:37
Syntheses of Anthracyclines and Fredericamycin A via Strong Base-Induced Cycloaddition Reaction of He manner. Thereactions have been applied to the syntheses of biologically important natural products. This review focuseson the following topics: (i)?preparation of homophthalic anhydrides from homophthalic acids using(trimethylsilyl)ethoxyacetylene, (ii)?strong base-induced cycloaddition of homopht作者: cardiopulmonary 時間: 2025-3-23 05:34 作者: 真實的你 時間: 2025-3-23 10:40 作者: 帶來墨水 時間: 2025-3-23 14:59 作者: Neuralgia 時間: 2025-3-23 19:28 作者: 容易做 時間: 2025-3-24 01:45 作者: 預測 時間: 2025-3-24 03:18
Synthesis of the Sugar Moietiesresented and their capability for scale-up andprocess development are commented upon. Rational sugar structural modifications, which are eitheruseful for synthetic purposes or offer advantages in experimental therapy of cancer, are discussedfrom the chemical point of view.作者: modifier 時間: 2025-3-24 08:00 作者: 按時間順序 時間: 2025-3-24 13:23 作者: 鉆孔 時間: 2025-3-24 18:50
https://doi.org/10.1007/978-3-663-13473-2of the biosynthetic pathwaysof anthracyclines have been made. Insights into the mechanistic features of the enzymes involvedare expected to have implications for the production of novel compounds with improved therapeuticprofiles by combinatorial biosynthesis.作者: 會議 時間: 2025-3-24 22:38
https://doi.org/10.1007/978-3-476-99781-4halic anhydrideswith the carbon–carbon double bond and the reaction mechanism, especially addressing the regiochemistryof the reaction, and (iii)?application of the reaction to the efficient asymmetric syntheses of anthracyclinesand fredericamycin?A.作者: 約會 時間: 2025-3-25 00:05
https://doi.org/10.1007/978-3-540-75815-0Base; Chemical synthesis; Cycloaddition; DNA; Enantiomer; biology; enzymes作者: 糾纏,纏繞 時間: 2025-3-25 05:34
978-3-642-09496-5Springer-Verlag Berlin Heidelberg 2008作者: 庇護 時間: 2025-3-25 08:41 作者: 運動性 時間: 2025-3-25 14:06
Topics in Current Chemistryhttp://image.papertrans.cn/a/image/158256.jpg作者: 易受刺激 時間: 2025-3-25 15:52 作者: MELD 時間: 2025-3-25 21:01 作者: needle 時間: 2025-3-26 02:00 作者: 沙漠 時間: 2025-3-26 05:53 作者: Density 時間: 2025-3-26 09:29 作者: minimal 時間: 2025-3-26 16:37 作者: 制定 時間: 2025-3-26 17:01
Der volkswirtschaftliche Kreislauf,d therapeutic efficacy and reduced cardiotoxicity stimulatedconsiderable efforts in the synthesis of new analogues. Since the biological activity of anthracyclinesdepends on their natural absolute configuration, various strategies for the synthesis of enantiomericallypure anthracyclinones (aglycones作者: conifer 時間: 2025-3-26 22:35
Diagnostik erblicher KrankheitenAlder additions with large reactivity difference betweenthe addition of the first equivalent (..) andthe second equivalent (..) of dienophile. Thisallows one to prepare, through parallel synthesis, a?large number of linearly condensed polycyclicsystems containing three annulated six-membered rings, 作者: CLAIM 時間: 2025-3-27 03:37 作者: 公式 時間: 2025-3-27 07:33
,Ideologien und Identit?tskonstruktionen,tructure. Modification or switch of the saccharidemoiety became an important line of new drug discovery and study of their mechanism of action. Naturalglycons (sugar moieties) of the anthracycline antibiotics belong to the 2,6-dideoxypyranose familyand their principal representative, daunosamine, is作者: 鋼筆記下懲罰 時間: 2025-3-27 12:45
,Ideologien und Identit?tskonstruktionen,a?sequence-selective manner, leading to inhibitionof DNA cleavage by DNase?I, whereas other hybrids cleaved DNA with base selectivity upon photoirradiation.This hybrid system was found to be very important for both DNA binding and photocleaving.作者: 揉雜 時間: 2025-3-27 14:27
https://doi.org/10.1007/978-3-476-99781-4e manner. Thereactions have been applied to the syntheses of biologically important natural products. This review focuseson the following topics: (i)?preparation of homophthalic anhydrides from homophthalic acids using(trimethylsilyl)ethoxyacetylene, (ii)?strong base-induced cycloaddition of homopht作者: FLACK 時間: 2025-3-27 20:11 作者: CEDE 時間: 2025-3-27 21:58
0340-1022 Overview: This series presents critical reviews of the present position and future trends in modern chemical research.Short and concise reports on chemistry, each written by the world renowned experts.Still val978-3-642-09496-5978-3-540-75815-0Series ISSN 0340-1022 Series E-ISSN 1436-5049 作者: bromide 時間: 2025-3-28 03:11 作者: 大暴雨 時間: 2025-3-28 09:54
Krankheiten der Nerven und des Geistesh for both increased potency and a?more favorablemetabolic pathway..This chapter aims to offer an updated overview of the efforts made by several research groups in thefield of fluorinated anthracyclines. We also give, along with the structures, brief descriptions of thesyntheses and current status of development.作者: trigger 時間: 2025-3-28 12:55 作者: ENACT 時間: 2025-3-28 15:55
Combinatorial Synthesis of Linearly Condensed Polycyclic Compounds, Including Anthracyclinones, Throtution of the double diene by arenesulfenylsubstituents. Enantiomerically pure anthracyclinones and analogues are obtained using enantiomericallypure dienophiles such as 3-oxo-but-2-en-2-yl esters. The chemistry so-developed has allowed the preparationof enantiomerically pure 6-((aminoalkoxy)oxy)met作者: 愛哭 時間: 2025-3-28 21:00 作者: 口味 時間: 2025-3-29 00:08
10樓作者: 免費 時間: 2025-3-29 05:27
10樓作者: 欄桿 時間: 2025-3-29 09:18
10樓
