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Organic Name Reactions: Principles, Mechanisms and Applications
Author(s) :Sanjay B. Bari, Vinod G. Ugale


ISBN : 9789389354737
Name : Organic Name Reactions: Principles, Mechanisms and Applications
Price : 495.00
Author/s : Sanjay B. Bari, Vinod G. Ugale
Type : Text Book
Pages : 478
Year of Publication : 2020
Publisher : PharmaMed Press / BSP Books
Binding : Paperback
Table of Contents : Click here
Chapter1 : Click here
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About the Book:

Special features of the book

We have divided every organic reaction in following subsections:

It is hope that this type of presentation will greatly aid the memory and understanding of students.

Principle: Includes text and general reactions with examples. We have indicated changes in functional groups while conversion of reactants into final products with the use of advanced ChemBioDraw Ultra tool. The text of manuscript has been made simple and lucid with pictorial presentations.

Mechanism: Includes text and detailed stepwise mechanism by highlighting the changes in reactants at every step. The context includes beautiful and clear representation of mechanisms; each step is shown without using any shortcuts. Lone pairs and reaction arrows are indicated clearly by using ChemBioDraw Ultra, making the mechanism easier to follow and understand thoroughly.

Applications: Includes text and utility of particular reaction in synthesis of useful product. We have also included stereochemical aspects and orientations for reactions along with its synthetic applications, where it is necessary. Inspite of refreshing the current understanding of name reactions, we have tried to incorporate latest synthetic industrial applications, so that it will help the learners who involved in synthetic research, early career researchers and at large to scientific community.

Contents:


1. Acyloin Condensation 2. Alder-Ene Reaction (Conia Reaction) 3. Alder-Rickert Reaction 4. Allan-Robinson Condensation 5. Aldol Condensation 6. Allylic Rearrangement 7. Amdori Glucosamine Rearrangement 8. Angeli-Remini Reaction 9. Anschutz Anthracene Synthesis 10. Appel Reaction 11. Arndt-Eistert Synthesis 12. Aston-Greenburg Rearrangement 13. Aza-Claisen Rearrangement 14. Baeyer Indole Synthesis 15. Baeyer Oxindole Synthesis 16. Baeyer Pyridine Synthesis 17. Baeyer-Villiger Oxidation 18. Baltz-Schiemann Reaction 19. Baker-Venkataraman Rearrangement 20. Bamberger Rearrangement 21. Barbier Reaction 22. Barton Reaction 23. Barton-Zard Pyrrole Synthesis 24. Bartoli Indole Synthesis 25. Baumann-Fromm Thiophene Synthesis 26. Beckmann Rearrangement 27. Benzidine Rearrangement 28. Benzilic Acid Rearrangement 29. Benzoin Condensation 30. Birch Reduction (Metal – Ammonia Reduction) 31. Bischler-Napieralski Reaction 32. Blaise Reaction 33. Bohlmann-Rahtz Pyridine Synthesis 34. Bodroux Amide Synthesis 35. Bouveault Aldehydes Synthesis 36. Bouveault-Blanc Reduction 37. Bruckner Isoquinoline Synthesis 38. Bucherer Carbazole Synthesis 39. Cadiot-Chodkiewicz Coupling 40. Cannizzaro Reaction 41. Carbylamine Reaction 42. Carroll Rearrangement 43. Chichibabin Amination Reaction 44. Chichibabin Pyridine Synthesis 45. Chugaev Elimination 46. Claisen Condensation 47. Claisen Rearrangement 48. Claisen-Schimdt Reaction 49. Clemmensen Reduction 50. Combes Quinoline Synthesis 51. Cope Elimination 52. Cope, Oxy-Cope, and Anionic Oxy-Cope Rearrangements 53. Corey-Bakshi-Shibata Reduction 54. Corey-House Synthesis 55. Criegee Mechanism of Ozonolysis 56. Cumene Hydroperoxide Rearrangement 57. Curtius Rearrangement 58. Dakin Reaction 59. Darzens Glycidic Ester Condensation 60. Diazotisation 61. Dieckmann Condensation 62. Diels-Alder Reaction 63. Dienol-Benzene Rearrangement 64. Dienone-Phenol Rearrangement 65. Doebner Reaction 66. Duff Reaction 67. Elbs Persulphate Oxidation 68. Elimination Reaction (E-1/E-2 Reaction) 69. Ester Pyrolysis 70. Etard Reaction 71. Favorskii reaction 72. Fischer Indole Synthesis 73. Fisher Oxazole Synthesis 74. Fischer-Speier Esterification 75. Fittig’s Synthesis 76. Fukuyama Amine Synthesis 77. Fukuyama Indole Synthesis 78. Friedel-Crafts Acylation 79. Friedel-Crafts Alkylation 80. Friedlander Quinoline Synthesis 81. Fries Rearrangement 82. Gabriel Phthalimide Synthesis (Gabriel Primary Amine Synthesis) 83. Gassman Indole Synthesis 84. Gassman Oxindole Synthesis 85. Gatterman Aldehyde Synthesis 86. Gattermann-Koch Reaction 87. Gomberg-Bachmann Reaction 88. Grignard Degradation 89. Grignard Reaction 90. Hantzsch Pyridine Synthesis 91. Hantzsch Pyrrole Synthesis 92. Hantzsch Thiazole Synthesis 93. Haworth Synthesis 94. Heck Reaction 95. Hell-Volhard-Zelinsky Reaction (HVZ Reaction) 96. Henry Reaction (Nitro Aldol Reaction) 97. Heron Rearrangement 98. Herz Reaction 99. Heyns Rearrangement 100. Hinsberg Reaction 101. Hinsberg Sulfone synthesis102. Hinsberg Thiophene synthesis 103. Hock Rearrangement 104. Hofmann Degradation Reaction 105. Hoffmann Rule Hoffmann Elimination 106. Hoffmann-Martius Rearrangement 107. Houben-Hoesch Reaction 108. Hunsdiecker Condensation 109. Hunsdiecker Reaction 110. Jacobsen Rearrangement 111. Jones Oxidation 112. Kharasch Addition Reaction 113. Kiliani-Fischer of Aldoses Synthesis 114. Knoevenagel Condensation 115. Koch-Haaf Carbonylation Reaction 116. Kochi Reaction 117. Kolbe Electrolysis Reaction 118. Kolbe-Schmitt Reaction 119. Lander Rearrangement 120. Larock Indole Synthesis 121. Lawesson's Reagent Synthesis 122. Leuckart’s Reaction 123. Leucart-Wallach reaction 124. Lindlar Hydrogenation 125. Lossen Rearrangement 126. Malaprade Reaction 127. Malonic Ester Synthesis 128. Mannich Reaction 129. Markovnikov's Rule 130. Mclafferty Rearrangement 131. Meerwein-Ponndorf-Verley Reduction 132. Michael Addition Reaction 133. Mitsunobu Reaction 134. Morin Rearrangement 135. Neber Rearrangement 136. Nef Reaction 137. Nucleophilic Substitution Reaction (SN1/SN2) 138. Oppenauer Oxidation 139. Orton Rearrangement 140. Overman Rearrangement 141. Paal-Knorr Furan Synthesis 142. Paal-Knorr Pyrrole Synthesis 143. Pechmann Condensation 144. Pechmann Pyrazole Synthesis 145. Perkins Reaction 146. Pinacol-Pinacolone Rearrangement 147. Prins Reaction 148. Pummerer Rearrangement 149. Reformatsky Reaction 150. Reimer-Tiemann Reaction 151. Reissert Indole Synthesis 152. Retro-Diels-Alder Reaction 153. Retro-Ene Reaction 154. Robinson Annulation 155. Rosenmund Reduction 156. Ruff Degradation 157. Sabatier-Senderens Reduction 158. Sandmeyer Isatin Synthesis 159. Sandmeyer Reaction 160. Saytzeff's Rule 161. Schmidt Reaction 162. Schotten-Baumann Reaction 163. Skraup Quinoline Synthesis 164. Smiles Rearrangement 165. Sommelet Reaction 166. Sommelet-Hauser Rearrangement 167. Staudinger [2 + 2] Cycloaddition Reaction 168. Staudinger Reduction Reaction 169. Stephen Reaction 170. Stevens Rearrangement 171. Stobbe Condensation 172. Stork Enamine Reaction 173. Strecker Synthesis 174. Suzuki Coupling 175. Swern Oxidation 176. Tiemann Cyanohydrin Amination 177. Tiemann Rearrangement 178. Tishchenko Reaction 179. Ugi Reaction 180. Ullmann Acridine Synthesis 181. Ullmann Reaction 182. Victor Meyer Reaction 183. Vilsmeier-Haack Reaction 184. Wacker Oxidation 185. Walden Inversion 186. Wagner-Meerwein Rearrangement 187. Wilkinson’s Catalyst 188. Willgerodt-Kindler Reaction 189. Williamson Synthesis of Ether 190. Wittig Reaction 191. [1,2]-Wittig Rearrangement 192. [2,3]-Wittig Rearrangement 193. Wohl-Ziegler Reaction 194. Wolff-Kishner Reduction 195. Wolff Rearrangement 196. Wurtz Reaction 197. Wurtz-Fittig Reaction 198. Yamaguchi Esterification 199. Ziegler-Hafner Azulene Synthesis 200. Ziegler-Natta Polymerization.

About the Authors:

S. B. Bari has a commendable track record of achievements and success in his academic career in Pharmacy. He has completed B. Pharm. (1994) from Government College of Pharmacy, Karad and M. Pharm. in Medicinal and Pharmaceutical Chemistry (1996) from S. G. I. T. S., Indore (M.P.). He has been awarded Ph. D in Pharmaceutical Sciences (2006) under AICTE-QIP program from University College of Pharmaceutical Sciences, Kakatiya University, and Warangal (A.P.). He has started his teaching career from lecturer at Anuradha College of Pharmacy, Chikhli, Dist: Buldana (M.S.). Then he worked as Assistant Professor, Professor, Vice Principal, Head of Department, Department of Pharmaceutical Chemistry, at R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur. Presently Dr. Bari is serving as Principal and Professor at premier institute an ISO 9001:2008 certified H. R. Patel Institute of Pharmaceutical Education and Research, Shirpur Dist: Dhule (M.S.). He has 22 years of teaching experience.

            He has more than 156 review and research publications in various renowned national, international levels. He has presented several papers at national and international conferences, ten books and filed     03 patents to his credit. He has received “National Merit Scholarship' from XIth to B.

Pharm., Junior Research Fellowship (Gate-94-M.Pharm.), Ph. D (AICTE-QIP Fellowship), V-life Sciences best publication Award 2012, Dr. P.D. Sethi Annual Award 2011-A certificate of merit for research paper, International Achievers Award 2015 by Utkarsh and Manavseva Vikas Foundation at National Achiever's Summit, Aurangabad.

            He has supervised 65 at M. Pharm. level Projects and 11 Ph. D students in Pharmacy. His Ph.D. students received several awards like Eli-Lilly and Company Asia Outstanding Thesis (Ph.D) Award (2011), Fast Track Young Scientist (2009) DST Fellowship and Rajiv Gandhi National Fellowship (2008), UGC, New Delhi.

            He is member and faculty member of BOS, Pharmaceutical chemistry at NMU, Jalgaon. He is a Life member of various professional associations like ISTE, IPA, APTI, ICS, IPS. Currently he is Co-ordinator, Faculty of Pharmacy, North Maharashtra University, Jalgaon.

Vinod G. Ugale was born and raised in Buldhana. He moved to the Amravati University to study pharmaceutical science (2007) and then read pharmaceutical chemistry at Nagpur University, Maharashtra (2009). He moved to North Maharashtra University, Jalgaon, achieving a Ph.D. in pharmaceutical chemistry under the supervision of Prof. Sanjay B. Bari. In his independent research career at North Maharashtra University in mid-2012, he set out to understand the organic and medicinal chemistry of nitrogen heterocyclic compounds. Vinod G. Ugale, PhD, is currently an Assistant Professor at Department of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, North Maharashtra University, Jalgaon, Maharashtra, India. He has been involved in teaching organic chemistry to undergraduate students from last ten years. He has published research papers, book chapters, and reviews in various reputed journals and has presented his works at several international platforms, for which he received awards by a different bodies. He is a member of professional and scientific societies, such as American Chemical Society (ACS) and Association of Pharmaceutical Teachers of India (APTI).
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