Organic Chemistry: 100 Must-Know Mechanisms / / Roman Valiulin.
This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with exp...
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Valiulin, Roman, author. aut http://id.loc.gov/vocabulary/relators/aut Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. Berlin ; Boston : De Gruyter, [2020] ©2020 1 online resource (X, 239 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda De Gruyter Textbook Frontmatter -- 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 & Malaprade Oxidation -- 30. CuAAC -- 31. Curtius Rearrangement -- 32. Darzens Condensation -- 33. Dess‒Martin Oxidation -- 34. Diazotization (Diazonium Salt) -- 34. Diazotization (Diazonium Salt) -- 36. Di‒π‒Methane Rearrangement -- 37. Favorskii Rearrangement -- 38. Fischer Indole Synthesis -- 39. Friedel‒Crafts Acylation & 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 -- 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 & II Reaction -- 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 -- 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 This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information. 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 27. Jan 2023) Organische Chemie. Organische Synthese. Reaktionsmechanismus. SCIENCE / Chemistry / Organic. bisacsh Chemical Sythesis. Organic Chemistry. Reaction Mechanisms. Title is part of eBook package: De Gruyter DG Ebook Package English 2020 9783110696288 Title is part of eBook package: De Gruyter DG Plus DeG Package 2020 Part 1 9783110696271 Title is part of eBook package: De Gruyter De Gruyter English eBooks 2020 - UC 9783110659061 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2020 English 9783110704716 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2020 9783110704518 ZDB-23-DGG Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2020 English 9783110704754 Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2020 9783110704556 ZDB-23-DPC EPUB 9783110608519 print 9783110608304 https://doi.org/10.1515/9783110608373 https://www.degruyter.com/isbn/9783110608373 Cover https://www.degruyter.com/document/cover/isbn/9783110608373/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 -- 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 & Malaprade Oxidation -- 30. CuAAC -- 31. Curtius Rearrangement -- 32. Darzens Condensation -- 33. Dess‒Martin Oxidation -- 34. Diazotization (Diazonium Salt) -- 36. Di‒π‒Methane Rearrangement -- 37. Favorskii Rearrangement -- 38. Fischer Indole Synthesis -- 39. Friedel‒Crafts Acylation & 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 -- 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 & II Reaction -- 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 -- 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 -- 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 & Malaprade Oxidation -- 30. CuAAC -- 31. Curtius Rearrangement -- 32. Darzens Condensation -- 33. Dess‒Martin Oxidation -- 34. Diazotization (Diazonium Salt) -- 36. Di‒π‒Methane Rearrangement -- 37. Favorskii Rearrangement -- 38. Fischer Indole Synthesis -- 39. Friedel‒Crafts Acylation & 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 -- 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 & II Reaction -- 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 -- 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 |
2020 |
| physical |
1 online resource (X, 239 p.) Issued also in print. |
| contents |
Frontmatter -- 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 & Malaprade Oxidation -- 30. CuAAC -- 31. Curtius Rearrangement -- 32. Darzens Condensation -- 33. Dess‒Martin Oxidation -- 34. Diazotization (Diazonium Salt) -- 36. Di‒π‒Methane Rearrangement -- 37. Favorskii Rearrangement -- 38. Fischer Indole Synthesis -- 39. Friedel‒Crafts Acylation & 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 -- 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 & II Reaction -- 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 -- 97. Weinreb Ketone Synthesis -- 98. Wittig Reaction -- 99. Wohl–Ziegler Reaction -- 100. Wolff–Kishner Reduction -- Acknowledgments -- Bibliography and References |
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Dess‒Martin Oxidation -- </subfield><subfield code="t">34. Diazotization (Diazonium Salt) -- </subfield><subfield code="t">34. Diazotization (Diazonium Salt) -- </subfield><subfield code="t">36. Di‒π‒Methane Rearrangement -- </subfield><subfield code="t">37. Favorskii Rearrangement -- </subfield><subfield code="t">38. Fischer Indole Synthesis -- </subfield><subfield code="t">39. Friedel‒Crafts Acylation & 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 -- </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 & II Reaction -- </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 -- </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">This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information.</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 27. Jan 2023)</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">Chemical Sythesis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Organic Chemistry.</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 Ebook Package English 2020</subfield><subfield code="z">9783110696288</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 2020 Part 1</subfield><subfield code="z">9783110696271</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">De Gruyter English eBooks 2020 - 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