Organic Name Reactions: Principles, Mechanisms and Applications

<div><!--block--><strong>Special features of the book<br></strong>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.<br><strong>Contents:</strong><br><strong>1.</strong> Acyloin Condensation <strong>2.</strong> Alder-Ene Reaction (Conia Reaction) <strong>3.</strong> Alder-Rickert Reaction <strong>4.</strong> Allan-Robinson Condensation <strong>5.</strong> Aldol Condensation <strong>6.</strong> Allylic Rearrangement <strong>7.</strong> Amdori Glucosamine Rearrangement <strong>8.</strong> Angeli-Remini Reaction <strong>9.</strong> Anschutz Anthracene Synthesis <strong>10.</strong> Appel Reaction <strong>11.</strong> Arndt-Eistert Synthesis <strong>12.</strong> Aston-Greenburg Rearrangement <strong>13.</strong> Aza-Claisen Rearrangement <strong>14.</strong> Baeyer Indole Synthesis <strong>15.</strong> Baeyer Oxindole Synthesis <strong>16.</strong> Baeyer Pyridine Synthesis <strong>17.</strong> Baeyer-Villiger Oxidation <strong>18.</strong> Baltz-Schiemann Reaction <strong>19.</strong> Baker-Venkataraman Rearrangement <strong>20.</strong> Bamberger Rearrangement <strong>21.</strong> Barbier Reaction <strong>22.</strong> Barton Reaction <strong>23.</strong> Barton-Zard Pyrrole Synthesis <strong>24.</strong> Bartoli Indole Synthesis <strong>25.</strong> Baumann-Fromm Thiophene Synthesis <strong>26.</strong> Beckmann Rearrangement <strong>27.</strong> Benzidine Rearrangement <strong>28.</strong> Benzilic Acid Rearrangement <strong>29.</strong> Benzoin Condensation <strong>30.</strong> Birch Reduction (Metal – Ammonia Reduction) <strong>31.</strong> Bischler-Napieralski Reaction <strong>32.</strong> Blaise Reaction <strong>33.</strong> Bohlmann-Rahtz Pyridine Synthesis <strong>34.</strong> Bodroux Amide Synthesis <strong>35.</strong> Bouveault Aldehydes Synthesis <strong>36.</strong> Bouveault-Blanc Reduction <strong>37.</strong> Bruckner Isoquinoline Synthesis <strong>38.</strong> Bucherer Carbazole Synthesis <strong>39.</strong> Cadiot-Chodkiewicz Coupling <strong>40.</strong> Cannizzaro Reaction <strong>41.</strong> Carbylamine Reaction <strong>42.</strong> Carroll Rearrangement <strong>43.</strong> Chichibabin Amination Reaction <strong>44.</strong> Chichibabin Pyridine Synthesis <strong>45.</strong> Chugaev Elimination <strong>46.</strong> Claisen Condensation <strong>47.</strong> Claisen Rearrangement <strong>48.</strong> Claisen-Schimdt Reaction <strong>49.</strong> Clemmensen Reduction <strong>50.</strong> Combes Quinoline Synthesis <strong>51.</strong> Cope Elimination <strong>52.</strong> Cope, Oxy-Cope, and Anionic Oxy-Cope Rearrangements <strong>53.</strong> Corey-Bakshi-Shibata Reduction <strong>54.</strong> Corey-House Synthesis <strong>55.</strong> Criegee Mechanism of Ozonolysis <strong>56.</strong> Cumene Hydroperoxide Rearrangement <strong>57.</strong> Curtius Rearrangement <strong>58.</strong> Dakin Reaction <strong>59.</strong> Darzens Glycidic Ester Condensation <strong>60.</strong> Diazotisation <strong>61.</strong> Dieckmann Condensation <strong>62.</strong> Diels-Alder Reaction <strong>63.</strong> Dienol-Benzene Rearrangement <strong>64.</strong> Dienone-Phenol Rearrangement <strong>65.</strong> Doebner Reaction <strong>66.</strong> Duff Reaction <strong>67.</strong> Elbs Persulphate Oxidation <strong>68.</strong> Elimination Reaction (E-1/E-2 Reaction) <strong>69.</strong> Ester Pyrolysis <strong>70.</strong> Etard Reaction <strong>71.</strong> Favorskii reaction <strong>72.</strong> Fischer Indole Synthesis <strong>73.</strong> Fisher Oxazole Synthesis <strong>74.</strong> Fischer-Speier Esterification <strong>75.</strong> Fittig’s Synthesis <strong>76.</strong> Fukuyama Amine Synthesis <strong>77.</strong> Fukuyama Indole Synthesis <strong>78.</strong> Friedel-Crafts Acylation <strong>79.</strong> Friedel-Crafts Alkylation <strong>80.</strong> Friedlander Quinoline Synthesis <strong>81.</strong> Fries Rearrangement <strong>82.</strong> Gabriel Phthalimide Synthesis (Gabriel Primary Amine Synthesis) <strong>83.</strong> Gassman Indole Synthesis <strong>84.</strong> Gassman Oxindole Synthesis <strong>85.</strong> Gatterman Aldehyde Synthesis <strong>86.</strong> Gattermann-Koch Reaction <br><strong>About the Authors:<br>S. B. Bari</strong> 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.<br /> <br /> <br /> <br /> <br /> <br /> 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<br /> <br /> <br />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.<br /> <br /> <br /> <br /> <br /> <br /> 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.<br /> <br /> <br /> <br /> <br /> <br /> 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.<br><br></div>