The series Topics in Current Chemistry Collections presents critical reviews from the journal Topics in Current Chemistry organized in topical volumes. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience.
Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.
Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.
1;Contents;62;Preface;83;Analysis of US FDA-Approved Drugs Containing Sulfur Atoms;103.1;Abstract;103.2;1 Introduction;113.3;2 Diversity of Sulfur-Containing Functional Groups in US FDA Drugs;113.3.1;2.1 Sulfonamides;113.3.2;2.2 ?-Lactams;183.3.3;2.3 Thioethers;213.3.4;2.4 Thiazoles;243.3.5;2.5 Thiophenes;263.3.6;2.6 Phenothiazines;283.3.7;2.7 Sulfoxides;293.3.8;2.8 C=S and P=S Structures;313.3.9;2.9 Thionucleotides;333.3.10;2.10 Sulfones;343.3.11;2.11 Sulfates;353.3.12;2.12 Macrocyclic Disulfides;373.3.13;2.13 Miscellaneous Acyclic Sulfur Functional Groups;383.3.14;2.14 Miscellaneous Cyclic Sulfur Functional Groups;393.4;3 US FDA Drugs Containing Multiple Sulfur Atoms;413.5;4 Presence of Sulfur Atoms in Combination Drugs;413.6;5 Conclusion;423.7;Acknowledgements;423.8;References;424;Sulfur-Containing Agrochemicals;444.1;Abstract;444.2;Introduction;454.3;Sulfonylureas;484.3.1;Sulfonylurea Herbicides;484.3.2;Sulfonylamino-Carbonyl-Triazolinones Herbicides;544.4;Sulfonamides;554.4.1;Sulfonamide Herbicides;554.4.2;Triazolopyrimidine Sulfonamide Herbicides;574.4.3;Sulfonamide Herbicide Safeners;584.4.4;Sulfonamide Fungicides;604.4.5;Sulfamide Fungicides;604.5;Sulfur-Containing Heterocyclics;614.5.1;Thiazole Fungicides;614.5.2;Thiazole Insecticides;634.5.3;Thiazole Herbicide Safener;654.5.4;Benzothiazole Herbicides;664.5.5;Thiazolidine Fungicides;674.5.6;Thiazolidine Insecticides;674.5.7;Thiophene Fungicides;684.5.8;Thiophene Nematicide;694.6;Thioureas;704.7;Sulfides, Sulfoxides, Sulfones;714.7.1;Methylthio-S-Triazine Herbicides;714.7.2;Sulfonyl-Isoxazoline Herbicides;724.7.3;Methyl Sulfone-Containing Herbicides;734.7.4;Sulfonyl--Triazole--Carboxamide Herbicides;764.7.5;Sulfone Nematicide;774.8;Sulfoximines;784.9;Conclusions;784.10;Acknowledgements;794.11;References;795;Thiophene-Based Organic Semiconductors;885.1;Abstract;885.2;Introduction;885.3;Thiophene;895.4;Thiophene-Based Small Molecules/Oligomers As Organic Semiconductors;915.4.1;Organic Photovoltaics;925.4.2;Organic Field-Effect Transistors;965.4.3;Organic Light-Emitting Diodes;985.5;Fused Thiophene-Based Small Molecules As Organic Semiconductors;1015.5.1;Organic Photovoltaics;1025.5.2;Organic Field-Effect Transistors;1075.5.3;Organic Light-Emitting Diodes;1105.6;Thiophene and Fused Thiophene-Based Polymers as Organic Semiconductors;1135.6.1;Organic Photovoltaics;1145.6.2;Organic Field-Effect Transistors;1205.6.3;Organic Light-Emitting Diodes;1225.7;Conclusions;1265.8;References;1276;Synthesis and Applications of Polymers Made by Inverse Vulcanization;1336.1;Abstract;1336.2;1 Synthesis of Polymers by Inverse Vulcanization;1336.3;2 Applications of Polymers Prepared by Inverse Vulcanization;1386.3.1;2.1 Cathode Materials for Li-S Batteries;1386.3.2;2.2 Dynamic and Repairable Materials;1406.3.3;2.3 Optics Applications;1436.3.4;2.4 Metal Sorption;1476.3.5;2.5 Oil Spill Remediation;1516.3.6;2.6 Controlled-Release Fertilizers;1516.4;3 Other Applications and Outlook;1546.5;Acknowledgements;1576.6;References;1577;Engineered C-S Bond Construction;1607.1;Abstract;1607.2;1 Introduction;1617.2.1;1.1 Importance of Thioethers;1617.3;2 First-Row 3d Series Transition-Metal Catalysis;1627.3.1;2.1 Fe, Mn, and Co-Catalyzed Reactions in C-S Bond Formation;1627.3.2;2.2 Ni and Cu Catalysis in C-S Coupling Reactions;1667.4;3 Second-Row 4d Series Transition-Metal Catalysis;1797.4.1;3.1 Pd- and Ru-Catalyzed Reactions in C-S Bond Formation;1797.4.2;3.2 Rh and Ag Catalysis in C-S Coupling Reactions;1837.5;4 Third-Row 5d Series Transition-Metal Catalysis;1847.5.1;4.1 La and Au Catalysis in C-S Bond Formation;1847.6;5 Post-Transition Metal Catalysis;1857.6.1;5.1 In and Bi Catalysis in C-S Cross-Coupling Reactions;1857.7;6 Alternative Systems for C-S bond Formation by Using Different Sulfur-Containing Surrogates;1867.7.1;6.1 Thiol as Sulfur-Containing Precursor;1877.7.2;6.2 Disulfide and Sulfoxide as
Jiang, Xuefeng
| ISBN | 9783030255985 |
|---|---|
| Artikelnummer | 9783030255985 |
| Medientyp | E-Book - PDF |
| Copyrightjahr | 2019 |
| Verlag | Springer-Verlag |
| Umfang | 477 Seiten |
| Sprache | Englisch |
| Kopierschutz | Digitales Wasserzeichen |
