Green Approaches in Medicinal Chemistry for Sustainable Drug Design. Volume 2, Methods /
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| Другие авторы: | |
|---|---|
| Формат: | Электронный ресурс eКнига |
| Язык: | английский |
| Опубликовано: |
San Diego :
Elsevier,
2024.
|
| Редактирование: | 2nd edition. |
| Серии: | Advances in green and sustainable chemistry.
|
| Предметы: | |
| Online-ссылка: | ScienceDirect |
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| 245 | 0 | 0 | |a Green Approaches in Medicinal Chemistry for Sustainable Drug Design. |n Volume 2, |p Methods / |c edited by Bimal Krishna Banik. |
| 246 | 3 | 0 | |a Methods |
| 250 | |a 2nd edition. | ||
| 264 | 1 | |a San Diego : |b Elsevier, |c 2024. | |
| 300 | |a 1 online resource (658 p.). | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Advances in Green and Sustainable Chemistry | |
| 505 | 0 | |a Front Cover -- Green Approaches in Medicinal Chemistry for Sustainable Drug Design -- Copyright Page -- Contents -- List of contributors -- About the editor -- Preface -- Acknowledgment -- 1 Nanotechnology -- 1 Nanocatalyzed organic transformations for synthesis of drug-like small molecules with medicinally privileged heterocycles -- 1.1 Introduction -- 1.2 Functionalized five- and fused five-membered heterocycles -- 1.2.1 Synthesis of functionalized pyrroles -- 1.2.1.1 Catalysis with Nano-CoFe2O4 supported molybdenum ([CoFe2O4@SiO2-PrNH2-Mo(acac)2]) | |
| 505 | 8 | |a 1.2.2 Synthesis of functionalized imidazoles -- 1.2.2.1 Catalysis with Fe3O4-polyethylene glycol-Cu(Fe3O4-PEG-Cu)nanocomposites -- 1.2.3 Synthesis of functionalized pyrazolones -- 1.2.3.1 Catalysis with CuI nanoparticles -- 1.2.4 Synthesis of pyrido-fused thiazolidinones -- 1.2.4.1 Catalysis with copper nanoparticles -- 1.2.5 Synthesis of functionalized triazoles -- 1.2.5.1 Catalysis with silica-nanoparticle-supported copper-containing ionic liquid (SNIL-Cu(II)) -- 1.2.5.2 Catalysis with copper nanoparticles supported on CeO2 -- 1.2.5.3 Catalysis with copper nanoparticles on activated carbon | |
| 505 | 8 | |a 1.2.5.4 Catalysis with Cu(I)/Cu nanocatalysts -- 1.2.5.5 Catalysis withCu2O nanoparticles -- 1.2.5.6 Catalysis with Cu-doped Mesoporous Silica NPs (Cu-RMSN) -- 1.2.5.7 Catalysis with nanomagnetite-supported metal ions -- 1.2.6 Synthesis of functionalized tetrazoles -- 1.2.6.1 Catalysis with zinc sulfide nanoparticles -- 1.2.7 Synthesis of functionalized indoles -- 1.2.7.1 Catalysis with Fe3O4-OSO3H nanoparticles -- 1.2.8 Synthesis of pyrimidoisoindoles -- 1.2.8.1 Catalysis with gold (III) dipyridine complex immobilized on Fe3O4 magnetic nanoparticles | |
| 505 | 8 | |a 1.3 Functionalized six- and fused six-membered heterocycles -- 1.3.1 Synthesis of functionalized pyridines -- 1.3.1.1 Catalysis with ZnO nanoparticles -- 1.3.1.2 Catalysis with copper-doped mesoporous silica (Cu/SiO2)catalyst -- 1.3.2 Synthesis of dihydropyridines -- 1.3.2.1 Catalysis with magnetite/chitosan heterogeneous nanocatalyst -- 1.3.2.2 Catalysis with nanocrystalline copper(II) oxide (nano-CuO) -- 1.3.2.3 Catalysis with magnetite nanoparticle-supported ceria catalyst (Nanocat-Fe-Ce) -- 1.3.2.4 Catalysis with nano-Fe2O3 catalyst -- 1.3.3 Synthesis of tetrahydropyridines | |
| 505 | 8 | |a 1.3.3.1 Catalysis with ZnO nanoparticles -- 1.3.4 Synthesis of functionalized pyrimidines and fused pyrimidines -- 1.3.4.1 Catalysis with Dendrimer-PWAn nanocatalyst -- 1.3.4.2 Catalysis with nano-ZrO2 sulfuric acid -- 1.3.4.3 Catalysis with Irish Moss/Fe3O4 as nano-biocatalyst -- 1.3.4.4 Catalysis with titanium dioxide nanowires -- 1.3.5 Synthesis of quinolines -- 1.3.5.1 Catalysis with ZrO2/Fe3O4 magnetic nanoparticles -- 1.3.5.2 Catalysis with Ni°-nanoparticles -- 1.3.5.3 Catalysis with cysteine-ferrite magnetic nanoparticles -- 1.3.5.4 Catalysis with ZrO2/Fe3O4 magnetic nanoparticles | |
| 500 | |a 1.3.5.5 Catalysis with piperidine-4-carboxylic acid functionalized Fe3O4 nanoparticles | ||
| 650 | 0 | |a Pharmaceutical chemistry. | |
| 650 | 0 | |a Green chemistry. | |
| 650 | 0 | |a Drugs |x Design. | |
| 650 | 2 | |a Chemistry, Pharmaceutical |0 (DNLM)D002626 | |
| 650 | 2 | |a Drug Design |0 (DNLM)D015195 | |
| 650 | 6 | |a Chimie pharmaceutique. |0 (CaQQLa)201-0028674 | |
| 650 | 6 | |a Chimie verte. |0 (CaQQLa)201-0337434 | |
| 650 | 6 | |a Médicaments |x Conception. |0 (CaQQLa)201-0203461 | |
| 650 | 7 | |a Drugs |x Design |2 fast |0 (OCoLC)fst00898790 | |
| 650 | 7 | |a Green chemistry |2 fast |0 (OCoLC)fst00912867 | |
| 650 | 7 | |a Pharmaceutical chemistry |2 fast |0 (OCoLC)fst01060115 | |
| 700 | 1 | |a Banik, Bimal. | |
| 776 | 0 | 8 | |i Print version: |a Banik, Bimal |t Green Approaches in Medicinal Chemistry for Sustainable Drug Design |d San Diego : Elsevier,c2024 |z 9780443161643 |
| 830 | 0 | |a Advances in green and sustainable chemistry. | |
| 856 | 4 | 0 | |3 ScienceDirect |u https://www.sciencedirect.com/science/book/9780443161643 |