Green Approaches in Medicinal Chemistry for Sustainable Drug Design : Applications /
Gorde:
| Beste egile batzuk: | |
|---|---|
| Formatua: | eBook |
| Hizkuntza: | ingelesa |
| Argitaratua: |
San Diego :
Elsevier,
2024.
|
| Edizioa: | 2nd ed. |
| Saila: | Advances in Green and Sustainable Chemistry Series.
|
| Gaiak: | |
| Sarrera elektronikoa: | ScienceDirect |
| Etiketak: |
Etiketa erantsi
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| 001 | on1438668321 | ||
| 003 | OCoLC | ||
| 005 | 20260915095219.0 | ||
| 006 | m o d | ||
| 007 | cr cnu|||||||| | ||
| 008 | 240608s2024 cau o 000 0 eng d | ||
| 040 | |a EBLCP |b eng |c EBLCP |d OPELS |d OCLCO |d COR |d OCLCO |d OCLCQ |d OCLCL |d OCLCF |d OCLCO | ||
| 066 | |c (S | ||
| 020 | |a 9780443161674 | ||
| 020 | |a 0443161674 | ||
| 020 | |z 9780443161667 | ||
| 035 | |a (OCoLC)1438668321 | ||
| 050 | 4 | |a RS403 | |
| 082 | 0 | 4 | |a 615.19 |1 https://id.oclc.org/worldcat/ddc/E4bTrbhdcjy3hWWpQKYr7x4mXb |
| 245 | 0 | 0 | |a Green Approaches in Medicinal Chemistry for Sustainable Drug Design : |b Applications / |c edited by Bimal Krishna Banik. |
| 246 | 3 | |a Applications | |
| 250 | |a 2nd ed. | ||
| 260 | |a San Diego : |b Elsevier, |c 2024. | ||
| 300 | |a 1 online resource (699 p.). | ||
| 490 | 1 | |a Advances in Green and Sustainable Chemistry Series ; |v v.Volume 1 | |
| 500 | |a Description based upon print version of record. | ||
| 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 Chemical catalysis -- 1 Green metal catalyzed reactions under sustainable conditions toward medicinally potent biomolecules -- 1.1 Introduction -- 1.2 C-C coupling reactions -- 1.2.1 Suzuki-Miyaura coupling -- 1.2.2 Negishi and Stille couplings -- 1.2.3 Sonogashira coupling -- 1.2.4 Heck coupling -- 1.2.5 Decarboxylative C-C coupling -- 1.2.6 Kumada-Corriu coupling -- 1.2.7 Arylation of enolates | |
| 505 | 8 | |a 1.2.8 Hayashi-Miyaura reaction -- 1.2.9 Aromatic cyanation -- 1.3 Conclusion -- References -- Further reading -- 2 Graphene oxide and modified graphene oxide-mediated synthesis of medicinally active compounds -- 2.1 Introduction -- 2.2 One-pot multistep synthesis -- 2.3 Dehydrogenative coupling reactions -- 2.4 Oxidation and hydration reactions -- 2.5 Ring-opening reactions -- 2.6 Direct amidation of carboxylic acids with amines -- 2.7 Conclusions -- Acknowledgments -- References -- 3 Organocatalytic cycloaddition reaction: a gateway for molecular complexity -- 3.1 Introduction | |
| 505 | 8 | |a 3.2 [4+2] Cycloaddition reaction -- 3.3 [4+2] Cycloaddition via iminium ion activation -- 3.4 [4+2] Cycloaddition via enamine activation -- 3.5 Conclusions -- Acknowledgments -- References -- 2 Biocatalysis -- 4 Baker's yeast-induced synthesis of medicinally important compounds -- 4.1 Introduction -- 4.1.1 Procedure for generation of Baker's yeast -- 4.1.2 Properties of Baker's yeast -- 4.1.3 Advantages of Baker's yeast -- 4.1.4 Methods involved in organic synthesis via Baker's yeast -- 4.1.5 Role of Baker's yeast in organic synthesis -- 4.1.5.1 Synthesis of heterocyclic compounds | |
| 505 | 8 | |a 4.1.5.2.5 Reduction of methyl acetoacetate -- 4.1.5.3 Baker's yeast mediated reaction and synthesis of bioactive compounds -- 4.1.5.3.1 Synthesis of cinnamyl acetate -- 4.1.5.3.2 Synthesis of fenfluramine -- 4.1.5.4 Synthesis of artemisinin with Baker's yeast -- 4.1.5.5 Baker's yeast mediated reduction of carvone -- 4.1.5.6 Cyclization of Squalene-like substrates -- 4.1.5.7 Baker's yeast assisted synthesis of ephedrine -- 4.1.5.8 Baker's yeast assisted synthesis of denopamine -- 4.2 Future perspectives -- 4.3 Conclusions -- List of abbreviations -- References | |
| 500 | |a 5 New methods for the manufacturing of pharmaceuticals and their intermediates using lipase | ||
| 650 | 0 | |a Pharmaceutical chemistry. | |
| 650 | 2 | |a Chemistry, Pharmaceutical |0 (DNLM)D002626 | |
| 650 | 6 | |a Chimie pharmaceutique. |0 (CaQQLa)201-0028674 | |
| 650 | 7 | |a Pharmaceutical chemistry |2 fast |0 (OCoLC)fst01060115 | |
| 700 | 1 | |a Banik, Bimal K. |1 https://id.oclc.org/worldcat/entity/E39PCjvBhGTRMGtbKWB3GCgPYq | |
| 776 | 0 | 8 | |i Print version: |a Banik, Bimal Krishna |t Green Approaches in Medicinal Chemistry for Sustainable Drug Design |d San Diego : Elsevier,c2024 |
| 830 | 0 | |a Advances in Green and Sustainable Chemistry Series. | |
| 856 | 4 | 0 | |3 ScienceDirect |u https://www.sciencedirect.com/science/book/9780443161667 |
| 880 | 8 | |6 505-00/(S |a 4.1.5.1.1 Synthesis of pyridine scaffolds -- 4.1.5.1.2 Synthesis of pyrimidine derivatives -- 4.1.5.1.3 Synthesis of thiazolidinone derivatives -- 4.1.5.1.4 Synthesis of pyran scaffold -- 4.1.5.1.5 Synthesis of benzothiazoles -- 4.1.5.1.6 Synthesis of 2-oxazolines -- 4.1.5.1.7 Synthesis of pyrrole chromenes -- 4.1.5.2 Baker's yeast catalyzed chemical reactions -- 4.1.5.2.1 Reduction of a carbonyl to a hydroxyl group -- 4.1.5.2.2 Reduction of ethyl acetoacetate -- 4.1.5.2.3 Reduction of ketones catalyzed by Immobilized Baker's yeast -- 4.1.5.2.4 Reduction of prochiral β-ketoesters | |