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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Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2023] ©2023 |
Year of Publication: | 2023 |
Edition: | 2nd, Completely Revised Edition |
Language: | English |
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Valiulin, Roman, author. aut http://id.loc.gov/vocabulary/relators/aut Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. 2nd, Completely Revised Edition Berlin ; Boston : De Gruyter, [2023] ©2023 1 online resource (XXII, 267 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda De Gruyter Textbook Frontmatter -- Second Edition -- Preface and Overview -- Contents -- List of Acronyms and Abbreviations -- 1 Electrophilic Addition Mechanism -- 2 Nucleophilic Substitution Mechanism -- 3 Aromatic Electrophilic Substitution Mechanism -- 4 Aromatic Nucleophilic Substitution Mechanism -- 5 Aromatic Radical Nucleophilic Substitution Mechanism -- 6 Elimination Mechanism -- 7 Acyloin Condensation -- 8 Alkyne Zipper Reaction -- 9 Arbuzov Reaction -- 10 Arndt–Eistert Synthesis -- 11 Baeyer–Villiger Oxidation -- 12 Barton Decarboxylation -- 13 Baylis–Hillman Reaction -- 14 Beckmann Rearrangement -- 15 Benzoin Condensation -- 16 Benzyne Mechanism -- 17 Bergman Cyclization -- 18 Birch Reduction -- 19 Bischler‒Napieralski Cyclization -- 20 Brown Hydroboration -- 21 Buchwald–Hartwig Cross-Coupling -- 22 Cannizzaro Reaction -- 23 Chan–Evans–Lam Cross-Coupling -- 24 Chichibabin Amination -- 25 Claisen Condensation -- 26 Claisen Rearrangement -- 27 Cope Elimination -- 28 Cope Rearrangement -- 29 Criegee and Malaprade Oxidation -- 30 CuAAC -- 31 Curtius Rearrangement -- 32 Darzens Condensation -- 33 Dess–Martin Oxidation -- 34 Diazotization (Diazonium Salt) -- 35 Diels–Alder Cycloaddition -- 36 Di-π-Methane Rearrangement -- 37 Favorskii Rearrangement -- 38 Fischer Indole Synthesis -- 39 Friedel–Crafts Acylation and Alkylation -- 40 Gabriel Synthesis -- 41 Gewald Reaction -- 42 Glaser–Eglinton–Hay Coupling -- 43 Grignard Reaction -- 44 Grob Fragmentation -- 45 Haloform Reaction -- 46 Heck Cross-Coupling -- 47 Hell–Volhard–Zelinsky Reaction -- 48 Hiyama Cross-Coupling -- 49 Hofmann Elimination -- 50 Horner–Wadsworth–Emmons Olefination -- 51 Jones Oxidation -- 52 Kucherov Reaction -- 53 Kumada Cross-Coupling -- 54 Ley–Griffith Oxidation -- 55 Liebeskind–Srogl Cross-Coupling -- 56 Mannich Reaction -- 57 McMurry Coupling Fig. -- 58 Meerwein–Ponndorf–Verley Reduction -- 59 Michael Addition -- 60 Minisci Reaction -- 61 Mitsunobu Reaction -- 62 Miyaura Borylation -- 63 Mukaiyama RedOx Hydration -- 64 Nazarov Cyclization -- 65 Nef Reaction -- 66 Negishi Cross-Coupling -- 67 Norrish Type I and II Reactions -- 68 Olefin (Alkene) Metathesis -- 69 Oppenauer Oxidation -- 70 Ozonolysis -- 71 Paal–Knorr Syntheses -- 72 Paternò–Büchi Reaction -- 73 Pauson–Khand Reaction -- 74 Peptide (Amide) Coupling -- 75 Pictet–Spengler Reaction -- 76 Pinacol–Pinacolone Rearrangement -- 77 Polonovski Reaction -- 78 Prilezhaev Epoxidation -- 79 Prins Reaction -- 80 Pummerer Rearrangement -- 81 Ramberg–Bäcklund Rearrangement -- 82 Reformatsky Reaction -- 83 Robinson Annulation -- 84 Shapiro Reaction -- 85 Sonogashira Cross-Coupling -- 86 Staudinger Reaction -- 87 Steglich Esterification -- 88 Stille Cross-Coupling -- 89 Suzuki Cross-Coupling -- 90 Swern Oxidation -- 91 Ugi Reaction -- 92 Ullmann Aryl–Aryl Coupling -- 93 Upjohn Dihydroxylation -- 94 Vilsmeier–Haack Reaction -- 95 Wacker Oxidation -- 96 Wagner–Meerwein Rearrangement Fi -- 97 Weinreb Ketone Synthesis -- 98 Wittig Reaction -- 99 Wohl–Ziegler Reaction -- 100 Wolff–Kishner Reduction -- Acknowledgments -- Bibliography and References restricted access http://purl.org/coar/access_right/c_16ec online access with authorization star 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 Issued also in print. Mode of access: Internet via World Wide Web. In English. Description based on online resource; title from PDF title page (publisher's Web site, viewed 06. Mrz 2024) Chemistry, Organic. Reaction mechanisms (Chemistry). Kinetik. Organische Chemie. Organische Synthese. Reaktionsmechanismus. SCIENCE / Chemistry / Organic. bisacsh Organic Chernistry. Organic Synthesis. Reaction Mechanisms. Title is part of eBook package: De Gruyter DG Plus DeG Package 2023 Part 1 9783111175782 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 English 9783111319292 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 9783111318912 ZDB-23-DGG Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English 9783111319230 Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 9783111318660 ZDB-23-DPC EPUB 9783110787016 print 9783110786828 https://doi.org/10.1515/9783110786835 https://www.degruyter.com/isbn/9783110786835 Cover https://www.degruyter.com/document/cover/isbn/9783110786835/original |
language |
English |
format |
eBook |
author |
Valiulin, Roman, Valiulin, Roman, |
spellingShingle |
Valiulin, Roman, Valiulin, Roman, Organic Chemistry: 100 Must-Know Mechanisms / De Gruyter Textbook Frontmatter -- Second Edition -- Preface and Overview -- Contents -- List of Acronyms and Abbreviations -- 1 Electrophilic Addition Mechanism -- 2 Nucleophilic Substitution Mechanism -- 3 Aromatic Electrophilic Substitution Mechanism -- 4 Aromatic Nucleophilic Substitution Mechanism -- 5 Aromatic Radical Nucleophilic Substitution Mechanism -- 6 Elimination Mechanism -- 7 Acyloin Condensation -- 8 Alkyne Zipper Reaction -- 9 Arbuzov Reaction -- 10 Arndt–Eistert Synthesis -- 11 Baeyer–Villiger Oxidation -- 12 Barton Decarboxylation -- 13 Baylis–Hillman Reaction -- 14 Beckmann Rearrangement -- 15 Benzoin Condensation -- 16 Benzyne Mechanism -- 17 Bergman Cyclization -- 18 Birch Reduction -- 19 Bischler‒Napieralski Cyclization -- 20 Brown Hydroboration -- 21 Buchwald–Hartwig Cross-Coupling -- 22 Cannizzaro Reaction -- 23 Chan–Evans–Lam Cross-Coupling -- 24 Chichibabin Amination -- 25 Claisen Condensation -- 26 Claisen Rearrangement -- 27 Cope Elimination -- 28 Cope Rearrangement -- 29 Criegee and Malaprade Oxidation -- 30 CuAAC -- 31 Curtius Rearrangement -- 32 Darzens Condensation -- 33 Dess–Martin Oxidation -- 34 Diazotization (Diazonium Salt) -- 35 Diels–Alder Cycloaddition -- 36 Di-π-Methane Rearrangement -- 37 Favorskii Rearrangement -- 38 Fischer Indole Synthesis -- 39 Friedel–Crafts Acylation and Alkylation -- 40 Gabriel Synthesis -- 41 Gewald Reaction -- 42 Glaser–Eglinton–Hay Coupling -- 43 Grignard Reaction -- 44 Grob Fragmentation -- 45 Haloform Reaction -- 46 Heck Cross-Coupling -- 47 Hell–Volhard–Zelinsky Reaction -- 48 Hiyama Cross-Coupling -- 49 Hofmann Elimination -- 50 Horner–Wadsworth–Emmons Olefination -- 51 Jones Oxidation -- 52 Kucherov Reaction -- 53 Kumada Cross-Coupling -- 54 Ley–Griffith Oxidation -- 55 Liebeskind–Srogl Cross-Coupling -- 56 Mannich Reaction -- 57 McMurry Coupling Fig. -- 58 Meerwein–Ponndorf–Verley Reduction -- 59 Michael Addition -- 60 Minisci Reaction -- 61 Mitsunobu Reaction -- 62 Miyaura Borylation -- 63 Mukaiyama RedOx Hydration -- 64 Nazarov Cyclization -- 65 Nef Reaction -- 66 Negishi Cross-Coupling -- 67 Norrish Type I and II Reactions -- 68 Olefin (Alkene) Metathesis -- 69 Oppenauer Oxidation -- 70 Ozonolysis -- 71 Paal–Knorr Syntheses -- 72 Paternò–Büchi Reaction -- 73 Pauson–Khand Reaction -- 74 Peptide (Amide) Coupling -- 75 Pictet–Spengler Reaction -- 76 Pinacol–Pinacolone Rearrangement -- 77 Polonovski Reaction -- 78 Prilezhaev Epoxidation -- 79 Prins Reaction -- 80 Pummerer Rearrangement -- 81 Ramberg–Bäcklund Rearrangement -- 82 Reformatsky Reaction -- 83 Robinson Annulation -- 84 Shapiro Reaction -- 85 Sonogashira Cross-Coupling -- 86 Staudinger Reaction -- 87 Steglich Esterification -- 88 Stille Cross-Coupling -- 89 Suzuki Cross-Coupling -- 90 Swern Oxidation -- 91 Ugi Reaction -- 92 Ullmann Aryl–Aryl Coupling -- 93 Upjohn Dihydroxylation -- 94 Vilsmeier–Haack Reaction -- 95 Wacker Oxidation -- 96 Wagner–Meerwein Rearrangement Fi -- 97 Weinreb Ketone Synthesis -- 98 Wittig Reaction -- 99 Wohl–Ziegler Reaction -- 100 Wolff–Kishner Reduction -- Acknowledgments -- Bibliography and References |
author_facet |
Valiulin, Roman, Valiulin, Roman, |
author_variant |
r v rv r v rv |
author_role |
VerfasserIn VerfasserIn |
author_sort |
Valiulin, Roman, |
title |
Organic Chemistry: 100 Must-Know Mechanisms / |
title_full |
Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. |
title_fullStr |
Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. |
title_full_unstemmed |
Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. |
title_auth |
Organic Chemistry: 100 Must-Know Mechanisms / |
title_alt |
Frontmatter -- Second Edition -- Preface and Overview -- Contents -- List of Acronyms and Abbreviations -- 1 Electrophilic Addition Mechanism -- 2 Nucleophilic Substitution Mechanism -- 3 Aromatic Electrophilic Substitution Mechanism -- 4 Aromatic Nucleophilic Substitution Mechanism -- 5 Aromatic Radical Nucleophilic Substitution Mechanism -- 6 Elimination Mechanism -- 7 Acyloin Condensation -- 8 Alkyne Zipper Reaction -- 9 Arbuzov Reaction -- 10 Arndt–Eistert Synthesis -- 11 Baeyer–Villiger Oxidation -- 12 Barton Decarboxylation -- 13 Baylis–Hillman Reaction -- 14 Beckmann Rearrangement -- 15 Benzoin Condensation -- 16 Benzyne Mechanism -- 17 Bergman Cyclization -- 18 Birch Reduction -- 19 Bischler‒Napieralski Cyclization -- 20 Brown Hydroboration -- 21 Buchwald–Hartwig Cross-Coupling -- 22 Cannizzaro Reaction -- 23 Chan–Evans–Lam Cross-Coupling -- 24 Chichibabin Amination -- 25 Claisen Condensation -- 26 Claisen Rearrangement -- 27 Cope Elimination -- 28 Cope Rearrangement -- 29 Criegee and Malaprade Oxidation -- 30 CuAAC -- 31 Curtius Rearrangement -- 32 Darzens Condensation -- 33 Dess–Martin Oxidation -- 34 Diazotization (Diazonium Salt) -- 35 Diels–Alder Cycloaddition -- 36 Di-π-Methane Rearrangement -- 37 Favorskii Rearrangement -- 38 Fischer Indole Synthesis -- 39 Friedel–Crafts Acylation and Alkylation -- 40 Gabriel Synthesis -- 41 Gewald Reaction -- 42 Glaser–Eglinton–Hay Coupling -- 43 Grignard Reaction -- 44 Grob Fragmentation -- 45 Haloform Reaction -- 46 Heck Cross-Coupling -- 47 Hell–Volhard–Zelinsky Reaction -- 48 Hiyama Cross-Coupling -- 49 Hofmann Elimination -- 50 Horner–Wadsworth–Emmons Olefination -- 51 Jones Oxidation -- 52 Kucherov Reaction -- 53 Kumada Cross-Coupling -- 54 Ley–Griffith Oxidation -- 55 Liebeskind–Srogl Cross-Coupling -- 56 Mannich Reaction -- 57 McMurry Coupling Fig. -- 58 Meerwein–Ponndorf–Verley Reduction -- 59 Michael Addition -- 60 Minisci Reaction -- 61 Mitsunobu Reaction -- 62 Miyaura Borylation -- 63 Mukaiyama RedOx Hydration -- 64 Nazarov Cyclization -- 65 Nef Reaction -- 66 Negishi Cross-Coupling -- 67 Norrish Type I and II Reactions -- 68 Olefin (Alkene) Metathesis -- 69 Oppenauer Oxidation -- 70 Ozonolysis -- 71 Paal–Knorr Syntheses -- 72 Paternò–Büchi Reaction -- 73 Pauson–Khand Reaction -- 74 Peptide (Amide) Coupling -- 75 Pictet–Spengler Reaction -- 76 Pinacol–Pinacolone Rearrangement -- 77 Polonovski Reaction -- 78 Prilezhaev Epoxidation -- 79 Prins Reaction -- 80 Pummerer Rearrangement -- 81 Ramberg–Bäcklund Rearrangement -- 82 Reformatsky Reaction -- 83 Robinson Annulation -- 84 Shapiro Reaction -- 85 Sonogashira Cross-Coupling -- 86 Staudinger Reaction -- 87 Steglich Esterification -- 88 Stille Cross-Coupling -- 89 Suzuki Cross-Coupling -- 90 Swern Oxidation -- 91 Ugi Reaction -- 92 Ullmann Aryl–Aryl Coupling -- 93 Upjohn Dihydroxylation -- 94 Vilsmeier–Haack Reaction -- 95 Wacker Oxidation -- 96 Wagner–Meerwein Rearrangement Fi -- 97 Weinreb Ketone Synthesis -- 98 Wittig Reaction -- 99 Wohl–Ziegler Reaction -- 100 Wolff–Kishner Reduction -- Acknowledgments -- Bibliography and References |
title_new |
Organic Chemistry: 100 Must-Know Mechanisms / |
title_sort |
organic chemistry: 100 must-know mechanisms / |
series |
De Gruyter Textbook |
series2 |
De Gruyter Textbook |
publisher |
De Gruyter, |
publishDate |
2023 |
physical |
1 online resource (XXII, 267 p.) Issued also in print. |
edition |
2nd, Completely Revised Edition |
contents |
Frontmatter -- Second Edition -- Preface and Overview -- Contents -- List of Acronyms and Abbreviations -- 1 Electrophilic Addition Mechanism -- 2 Nucleophilic Substitution Mechanism -- 3 Aromatic Electrophilic Substitution Mechanism -- 4 Aromatic Nucleophilic Substitution Mechanism -- 5 Aromatic Radical Nucleophilic Substitution Mechanism -- 6 Elimination Mechanism -- 7 Acyloin Condensation -- 8 Alkyne Zipper Reaction -- 9 Arbuzov Reaction -- 10 Arndt–Eistert Synthesis -- 11 Baeyer–Villiger Oxidation -- 12 Barton Decarboxylation -- 13 Baylis–Hillman Reaction -- 14 Beckmann Rearrangement -- 15 Benzoin Condensation -- 16 Benzyne Mechanism -- 17 Bergman Cyclization -- 18 Birch Reduction -- 19 Bischler‒Napieralski Cyclization -- 20 Brown Hydroboration -- 21 Buchwald–Hartwig Cross-Coupling -- 22 Cannizzaro Reaction -- 23 Chan–Evans–Lam Cross-Coupling -- 24 Chichibabin Amination -- 25 Claisen Condensation -- 26 Claisen Rearrangement -- 27 Cope Elimination -- 28 Cope Rearrangement -- 29 Criegee and Malaprade Oxidation -- 30 CuAAC -- 31 Curtius Rearrangement -- 32 Darzens Condensation -- 33 Dess–Martin Oxidation -- 34 Diazotization (Diazonium Salt) -- 35 Diels–Alder Cycloaddition -- 36 Di-π-Methane Rearrangement -- 37 Favorskii Rearrangement -- 38 Fischer Indole Synthesis -- 39 Friedel–Crafts Acylation and Alkylation -- 40 Gabriel Synthesis -- 41 Gewald Reaction -- 42 Glaser–Eglinton–Hay Coupling -- 43 Grignard Reaction -- 44 Grob Fragmentation -- 45 Haloform Reaction -- 46 Heck Cross-Coupling -- 47 Hell–Volhard–Zelinsky Reaction -- 48 Hiyama Cross-Coupling -- 49 Hofmann Elimination -- 50 Horner–Wadsworth–Emmons Olefination -- 51 Jones Oxidation -- 52 Kucherov Reaction -- 53 Kumada Cross-Coupling -- 54 Ley–Griffith Oxidation -- 55 Liebeskind–Srogl Cross-Coupling -- 56 Mannich Reaction -- 57 McMurry Coupling Fig. -- 58 Meerwein–Ponndorf–Verley Reduction -- 59 Michael Addition -- 60 Minisci Reaction -- 61 Mitsunobu Reaction -- 62 Miyaura Borylation -- 63 Mukaiyama RedOx Hydration -- 64 Nazarov Cyclization -- 65 Nef Reaction -- 66 Negishi Cross-Coupling -- 67 Norrish Type I and II Reactions -- 68 Olefin (Alkene) Metathesis -- 69 Oppenauer Oxidation -- 70 Ozonolysis -- 71 Paal–Knorr Syntheses -- 72 Paternò–Büchi Reaction -- 73 Pauson–Khand Reaction -- 74 Peptide (Amide) Coupling -- 75 Pictet–Spengler Reaction -- 76 Pinacol–Pinacolone Rearrangement -- 77 Polonovski Reaction -- 78 Prilezhaev Epoxidation -- 79 Prins Reaction -- 80 Pummerer Rearrangement -- 81 Ramberg–Bäcklund Rearrangement -- 82 Reformatsky Reaction -- 83 Robinson Annulation -- 84 Shapiro Reaction -- 85 Sonogashira Cross-Coupling -- 86 Staudinger Reaction -- 87 Steglich Esterification -- 88 Stille Cross-Coupling -- 89 Suzuki Cross-Coupling -- 90 Swern Oxidation -- 91 Ugi Reaction -- 92 Ullmann Aryl–Aryl Coupling -- 93 Upjohn Dihydroxylation -- 94 Vilsmeier–Haack Reaction -- 95 Wacker Oxidation -- 96 Wagner–Meerwein Rearrangement Fi -- 97 Weinreb Ketone Synthesis -- 98 Wittig Reaction -- 99 Wohl–Ziegler Reaction -- 100 Wolff–Kishner Reduction -- Acknowledgments -- Bibliography and References |
isbn |
9783110786835 9783111175782 9783111319292 9783111318912 9783111319230 9783111318660 9783110787016 9783110786828 |
callnumber-first |
Q - Science |
callnumber-subject |
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callnumber-label |
QD251 |
callnumber-sort |
QD 3251.3 V35 42023 |
url |
https://doi.org/10.1515/9783110786835 https://www.degruyter.com/isbn/9783110786835 https://www.degruyter.com/document/cover/isbn/9783110786835/original |
illustrated |
Not Illustrated |
dewey-hundreds |
500 - Science |
dewey-tens |
540 - Chemistry |
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547 - Organic chemistry |
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547 |
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3547 |
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547 |
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10.1515/9783110786835 |
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Title is part of eBook package: De Gruyter DG Plus DeG Package 2023 Part 1 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 English Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 |
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Organic Chemistry: 100 Must-Know Mechanisms / |
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code="t">39 Friedel–Crafts Acylation and Alkylation -- </subfield><subfield code="t">40 Gabriel Synthesis -- </subfield><subfield code="t">41 Gewald Reaction -- </subfield><subfield code="t">42 Glaser–Eglinton–Hay Coupling -- </subfield><subfield code="t">43 Grignard Reaction -- </subfield><subfield code="t">44 Grob Fragmentation -- </subfield><subfield code="t">45 Haloform Reaction -- </subfield><subfield code="t">46 Heck Cross-Coupling -- </subfield><subfield code="t">47 Hell–Volhard–Zelinsky Reaction -- </subfield><subfield code="t">48 Hiyama Cross-Coupling -- </subfield><subfield code="t">49 Hofmann Elimination -- </subfield><subfield code="t">50 Horner–Wadsworth–Emmons Olefination -- </subfield><subfield code="t">51 Jones Oxidation -- </subfield><subfield code="t">52 Kucherov Reaction -- </subfield><subfield code="t">53 Kumada Cross-Coupling -- </subfield><subfield code="t">54 Ley–Griffith Oxidation -- </subfield><subfield code="t">55 Liebeskind–Srogl Cross-Coupling -- </subfield><subfield code="t">56 Mannich Reaction -- </subfield><subfield code="t">57 McMurry Coupling Fig. -- </subfield><subfield code="t">58 Meerwein–Ponndorf–Verley Reduction -- </subfield><subfield code="t">59 Michael Addition -- </subfield><subfield code="t">60 Minisci Reaction -- </subfield><subfield code="t">61 Mitsunobu Reaction -- </subfield><subfield code="t">62 Miyaura Borylation -- </subfield><subfield code="t">63 Mukaiyama RedOx Hydration -- </subfield><subfield code="t">64 Nazarov Cyclization -- </subfield><subfield code="t">65 Nef Reaction -- </subfield><subfield code="t">66 Negishi Cross-Coupling -- </subfield><subfield code="t">67 Norrish Type I and II Reactions -- </subfield><subfield code="t">68 Olefin (Alkene) Metathesis -- </subfield><subfield code="t">69 Oppenauer Oxidation -- </subfield><subfield code="t">70 Ozonolysis -- </subfield><subfield code="t">71 Paal–Knorr Syntheses -- </subfield><subfield code="t">72 Paternò–Büchi Reaction -- </subfield><subfield code="t">73 Pauson–Khand Reaction -- </subfield><subfield code="t">74 Peptide (Amide) Coupling -- </subfield><subfield code="t">75 Pictet–Spengler Reaction -- </subfield><subfield code="t">76 Pinacol–Pinacolone Rearrangement -- </subfield><subfield code="t">77 Polonovski Reaction -- </subfield><subfield code="t">78 Prilezhaev Epoxidation -- </subfield><subfield code="t">79 Prins Reaction -- </subfield><subfield code="t">80 Pummerer Rearrangement -- </subfield><subfield code="t">81 Ramberg–Bäcklund Rearrangement -- </subfield><subfield code="t">82 Reformatsky Reaction -- </subfield><subfield code="t">83 Robinson Annulation -- </subfield><subfield code="t">84 Shapiro Reaction -- </subfield><subfield code="t">85 Sonogashira Cross-Coupling -- </subfield><subfield code="t">86 Staudinger Reaction -- </subfield><subfield code="t">87 Steglich Esterification -- </subfield><subfield code="t">88 Stille Cross-Coupling -- </subfield><subfield code="t">89 Suzuki Cross-Coupling -- </subfield><subfield code="t">90 Swern Oxidation -- </subfield><subfield code="t">91 Ugi Reaction -- </subfield><subfield code="t">92 Ullmann Aryl–Aryl Coupling -- </subfield><subfield code="t">93 Upjohn Dihydroxylation -- </subfield><subfield code="t">94 Vilsmeier–Haack Reaction -- </subfield><subfield code="t">95 Wacker Oxidation -- </subfield><subfield code="t">96 Wagner–Meerwein Rearrangement Fi -- </subfield><subfield code="t">97 Weinreb Ketone Synthesis -- </subfield><subfield code="t">98 Wittig Reaction -- </subfield><subfield code="t">99 Wohl–Ziegler Reaction -- </subfield><subfield code="t">100 Wolff–Kishner Reduction -- </subfield><subfield code="t">Acknowledgments -- </subfield><subfield code="t">Bibliography and References</subfield></datafield><datafield tag="506" ind1="0" ind2=" "><subfield code="a">restricted access</subfield><subfield code="u">http://purl.org/coar/access_right/c_16ec</subfield><subfield code="f">online access with authorization</subfield><subfield code="2">star</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="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</subfield></datafield><datafield tag="530" ind1=" " ind2=" "><subfield code="a">Issued also in print.</subfield></datafield><datafield tag="538" ind1=" " ind2=" "><subfield code="a">Mode of access: Internet via World Wide Web.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">In English.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Description based on online resource; title from PDF title page (publisher's Web site, viewed 06. Mrz 2024)</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Chemistry, Organic.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Reaction mechanisms (Chemistry).</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Kinetik.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organische Chemie.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organische Synthese.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Reaktionsmechanismus.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE / Chemistry / Organic.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Organic Chernistry.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Organic Synthesis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Reaction Mechanisms.</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Title is part of eBook package:</subfield><subfield code="d">De Gruyter</subfield><subfield code="t">DG Plus DeG Package 2023 Part 1</subfield><subfield code="z">9783111175782</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Title is part of eBook package:</subfield><subfield code="d">De Gruyter</subfield><subfield code="t">EBOOK PACKAGE COMPLETE 2023 English</subfield><subfield code="z">9783111319292</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Title is part of eBook package:</subfield><subfield code="d">De Gruyter</subfield><subfield code="t">EBOOK PACKAGE COMPLETE 2023</subfield><subfield code="z">9783111318912</subfield><subfield code="o">ZDB-23-DGG</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Title is part of eBook package:</subfield><subfield code="d">De Gruyter</subfield><subfield code="t">EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English</subfield><subfield code="z">9783111319230</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Title is part of eBook package:</subfield><subfield code="d">De Gruyter</subfield><subfield code="t">EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023</subfield><subfield code="z">9783111318660</subfield><subfield code="o">ZDB-23-DPC</subfield></datafield><datafield tag="776" ind1="0" ind2=" "><subfield code="c">EPUB</subfield><subfield code="z">9783110787016</subfield></datafield><datafield tag="776" ind1="0" ind2=" "><subfield code="c">print</subfield><subfield code="z">9783110786828</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1515/9783110786835</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://www.degruyter.com/isbn/9783110786835</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="3">Cover</subfield><subfield code="u">https://www.degruyter.com/document/cover/isbn/9783110786835/original</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">978-3-11-117578-2 DG Plus DeG Package 2023 Part 1</subfield><subfield code="b">2023</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">978-3-11-131923-0 EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English</subfield><subfield code="b">2023</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">978-3-11-131929-2 EBOOK PACKAGE COMPLETE 2023 English</subfield><subfield code="b">2023</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_CL_CHCOMSGSEN</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_DGALL</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_EBKALL</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_ECL_CHCOMSGSEN</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_EEBKALL</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_ESTMALL</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">EBA_STMALL</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV-deGruyter-alles</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-23-DGG</subfield><subfield code="b">2023</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-23-DPC</subfield><subfield code="b">2023</subfield></datafield></record></collection> |