Organic Chemistry: 100 Must-Know Mechanisms / / Roman Valiulin.
In chemistry, good problem-solving requires a balanced combination of scientific intuition andmethodical analysis. Additionally, thoughtfully presented diagrams and infographics can conveya large amount of complex information in a more intuitive and accessible manner. 100 Must-KnowMechanisms (Second...
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| Superior document: | Title is part of eBook package: De Gruyter DG Plus DeG Package 2023 Part 1 |
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| Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2023] ©2023 |
| Year of Publication: | 2023 |
| Edition: | 2nd, Completely Revised Edition |
| Language: | English |
| Series: | De Gruyter Textbook
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| Online Access: | |
| Physical Description: | 1 online resource (XXII, 267 p.) |
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|---|---|---|---|
| 001 | 9783110786835 | ||
| 003 | DE-B1597 | ||
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| 100 | 1 | |a Valiulin, Roman, |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 245 | 1 | 0 | |a Organic Chemistry: 100 Must-Know Mechanisms / |c Roman Valiulin. |
| 250 | |a 2nd, Completely Revised Edition | ||
| 264 | 1 | |a Berlin ; |a Boston : |b De Gruyter, |c [2023] | |
| 264 | 4 | |c ©2023 | |
| 300 | |a 1 online resource (XXII, 267 p.) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 347 | |a text file |b PDF |2 rda | ||
| 490 | 0 | |a De Gruyter Textbook | |
| 505 | 0 | 0 | |t Frontmatter -- |t Second Edition -- |t Preface and Overview -- |t Contents -- |t List of Acronyms and Abbreviations -- |t 1 Electrophilic Addition Mechanism -- |t 2 Nucleophilic Substitution Mechanism -- |t 3 Aromatic Electrophilic Substitution Mechanism -- |t 4 Aromatic Nucleophilic Substitution Mechanism -- |t 5 Aromatic Radical Nucleophilic Substitution Mechanism -- |t 6 Elimination Mechanism -- |t 7 Acyloin Condensation -- |t 8 Alkyne Zipper Reaction -- |t 9 Arbuzov Reaction -- |t 10 Arndt–Eistert Synthesis -- |t 11 Baeyer–Villiger Oxidation -- |t 12 Barton Decarboxylation -- |t 13 Baylis–Hillman Reaction -- |t 14 Beckmann Rearrangement -- |t 15 Benzoin Condensation -- |t 16 Benzyne Mechanism -- |t 17 Bergman Cyclization -- |t 18 Birch Reduction -- |t 19 Bischler‒Napieralski Cyclization -- |t 20 Brown Hydroboration -- |t 21 Buchwald–Hartwig Cross-Coupling -- |t 22 Cannizzaro Reaction -- |t 23 Chan–Evans–Lam Cross-Coupling -- |t 24 Chichibabin Amination -- |t 25 Claisen Condensation -- |t 26 Claisen Rearrangement -- |t 27 Cope Elimination -- |t 28 Cope Rearrangement -- |t 29 Criegee and Malaprade Oxidation -- |t 30 CuAAC -- |t 31 Curtius Rearrangement -- |t 32 Darzens Condensation -- |t 33 Dess–Martin Oxidation -- |t 34 Diazotization (Diazonium Salt) -- |t 35 Diels–Alder Cycloaddition -- |t 36 Di-π-Methane Rearrangement -- |t 37 Favorskii Rearrangement -- |t 38 Fischer Indole Synthesis -- |t 39 Friedel–Crafts Acylation and Alkylation -- |t 40 Gabriel Synthesis -- |t 41 Gewald Reaction -- |t 42 Glaser–Eglinton–Hay Coupling -- |t 43 Grignard Reaction -- |t 44 Grob Fragmentation -- |t 45 Haloform Reaction -- |t 46 Heck Cross-Coupling -- |t 47 Hell–Volhard–Zelinsky Reaction -- |t 48 Hiyama Cross-Coupling -- |t 49 Hofmann Elimination -- |t 50 Horner–Wadsworth–Emmons Olefination -- |t 51 Jones Oxidation -- |t 52 Kucherov Reaction -- |t 53 Kumada Cross-Coupling -- |t 54 Ley–Griffith Oxidation -- |t 55 Liebeskind–Srogl Cross-Coupling -- |t 56 Mannich Reaction -- |t 57 McMurry Coupling Fig. -- |t 58 Meerwein–Ponndorf–Verley Reduction -- |t 59 Michael Addition -- |t 60 Minisci Reaction -- |t 61 Mitsunobu Reaction -- |t 62 Miyaura Borylation -- |t 63 Mukaiyama RedOx Hydration -- |t 64 Nazarov Cyclization -- |t 65 Nef Reaction -- |t 66 Negishi Cross-Coupling -- |t 67 Norrish Type I and II Reactions -- |t 68 Olefin (Alkene) Metathesis -- |t 69 Oppenauer Oxidation -- |t 70 Ozonolysis -- |t 71 Paal–Knorr Syntheses -- |t 72 Paternò–Büchi Reaction -- |t 73 Pauson–Khand Reaction -- |t 74 Peptide (Amide) Coupling -- |t 75 Pictet–Spengler Reaction -- |t 76 Pinacol–Pinacolone Rearrangement -- |t 77 Polonovski Reaction -- |t 78 Prilezhaev Epoxidation -- |t 79 Prins Reaction -- |t 80 Pummerer Rearrangement -- |t 81 Ramberg–Bäcklund Rearrangement -- |t 82 Reformatsky Reaction -- |t 83 Robinson Annulation -- |t 84 Shapiro Reaction -- |t 85 Sonogashira Cross-Coupling -- |t 86 Staudinger Reaction -- |t 87 Steglich Esterification -- |t 88 Stille Cross-Coupling -- |t 89 Suzuki Cross-Coupling -- |t 90 Swern Oxidation -- |t 91 Ugi Reaction -- |t 92 Ullmann Aryl–Aryl Coupling -- |t 93 Upjohn Dihydroxylation -- |t 94 Vilsmeier–Haack Reaction -- |t 95 Wacker Oxidation -- |t 96 Wagner–Meerwein Rearrangement Fi -- |t 97 Weinreb Ketone Synthesis -- |t 98 Wittig Reaction -- |t 99 Wohl–Ziegler Reaction -- |t 100 Wolff–Kishner Reduction -- |t Acknowledgments -- |t Bibliography and References |
| 506 | 0 | |a restricted access |u http://purl.org/coar/access_right/c_16ec |f online access with authorization |2 star | |
| 520 | |a In chemistry, good problem-solving requires a balanced combination of scientific intuition andmethodical analysis. Additionally, thoughtfully presented diagrams and infographics can conveya large amount of complex information in a more intuitive and accessible manner. 100 Must-KnowMechanisms (Second Edition) strives to be at the intersection of these two key principles. Itsthorough visualizations enable experienced readers to use it as a quick reference for specificmechanisms of interest. At the same time, the book’s breadth of covered reactions, from classic tocutting-edge, make it a good study-aid for the developing chemist. A slow and consistent study ofthe entire series of mechanisms can help set the foundation for good scientific intuition, while itsdetailed infographics and careful navigation features encourage coming back to it frequently. Thisedition includes over 40 new illustrations, numerous new mechanistic schemes, enhanced originalfigures with a variety of real-case examples, and more | ||
| 530 | |a Issued also in print. | ||
| 538 | |a Mode of access: Internet via World Wide Web. | ||
| 546 | |a In English. | ||
| 588 | 0 | |a Description based on online resource; title from PDF title page (publisher's Web site, viewed 06. Mrz 2024) | |
| 650 | 0 | |a Chemistry, Organic. | |
| 650 | 0 | |a Reaction mechanisms (Chemistry). | |
| 650 | 4 | |a Kinetik. | |
| 650 | 4 | |a Organische Chemie. | |
| 650 | 4 | |a Organische Synthese. | |
| 650 | 4 | |a Reaktionsmechanismus. | |
| 650 | 7 | |a SCIENCE / Chemistry / Organic. |2 bisacsh | |
| 653 | |a Organic Chernistry. | ||
| 653 | |a Organic Synthesis. | ||
| 653 | |a Reaction Mechanisms. | ||
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| 773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t EBOOK PACKAGE COMPLETE 2023 |z 9783111318912 |o ZDB-23-DGG |
| 773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English |z 9783111319230 |
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| 776 | 0 | |c EPUB |z 9783110787016 | |
| 776 | 0 | |c print |z 9783110786828 | |
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| 912 | |a 978-3-11-131929-2 EBOOK PACKAGE COMPLETE 2023 English |b 2023 | ||
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