Name Reactions in Organic Synthesis

Arun Parikh; Hansa Parikh; Khyati Parikh

doi:10.1017/UPO9788175968295

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Maddirala, Amarendar Reddy and Andreana, Peter R. 2016. Synthesis of 3‐Substituted 2‐Indolinones by a Multicomponent Coupling Isocyanide‐Dependent Microwave‐Assisted Intramolecular Transamidation Process. European Journal of Organic Chemistry, Vol. 2016, Issue. 1, p. 196.

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Capomolla, Simona S. Manfroni, Giacomo Prescimone, Alessandro Constable, Edwin C. and Housecroft, Catherine E. 2022. Versatility within (4,4) networks assembled from 1,4-bis(n-alkyloxy)-2,5-bis(3,2′:6′,3′'-terpyridin-4′-yl)benzene and [Cu(hfacac)2] (Hhfacac = 1,1,1,5,5,5-hexafluoropentane-2,4-dione). Polyhedron, Vol. 224, Issue. , p. 116005.

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Xia, Yun-Tao Wang, Xia Su, Ming-Hui Zhou, Jia-Yong Guo, Duo-Xin Zhang, Bin-Peng Sun, Wan-Peng Cui, Chen Yan, Meng and Li, Ya-Xin 2024. High turnover and selective Bin-Pd-NCs catalyst for nitro group non-hydrogen reductions in H2O under air conditions: A sustainable and recyclable route to aromatic amines. Journal of Catalysis, Vol. 437, Issue. , p. 115676.

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Arun Parikh, Retired Professor, Department of Chemistry, Saurashtra University, Hansa Parikh, Retired Professor, Department of Chemistry, Saurashtra University, Khyati Parikh, Retired Professor, Department of Chemistry, Saurashtra University

Publisher:: Foundation Books
Online publication date:: February 2012
Print publication year:: 2006
Online ISBN:: 9788175968295
DOI:: https://doi.org/10.1017/UPO9788175968295

Subjects:: Organic Chemistry, Chemistry

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The book focuses on main aspects of chemical reaction, i.e. principle, mechanism and applications of synthetic utility. The content is explained in an easy and simple language. It will be a good source of information for fundamental knowledge of organic synthesis to students at undergraduate level as well as industrial chemist.

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Name Reactions in Organic Synthesis

This Book has been cited by the following publications. This list is generated based on data provided by Crossref.

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Contents

Frontmatter
pp i-ii

Contents
pp iii-vii

Foreword
pp viii-viii

Preface
pp ix-x

Abbreviations and Acronyms
pp xi-xiv

PART I
pp 1-2

1 - Arndt-Eistert Reaction
pp 3-6

2 - Baeyer-Villiger Oxidation
pp 7-12

3 - Baker-Venkatraman Rearrangement
pp 13-16

4 - Baker's yeast Enzymatic Synthesis
pp 17-20

5 - Bamford-Stevens Reaction
pp 21-26

6 - Barbier-Wieland Degradation
pp 27-29

7 - Barbier Reaction
pp 30-31

8 - Bart Reaction
pp 32-34

9 - Barton Decarboxylation
pp 35-38

10 - Barton-McCombie Reaction
pp 39-42

11 - Barton Reaction
pp 43-44

12 - Baylis-Hillman Reaction
pp 45-49

13 - Bechamp Reaction
pp 50-52

14 - Bechamp Reduction
pp 53-53

15 - Beckmann Rearrangement
pp 54-59

16 - Benzilic Acid Rearrangement
pp 60-63

17 - Benzoin Condensation
pp 64-68

18 - Birch Reduction
pp 69-72

19 - Blanc Chloromethylation Reaction
pp 73-75

20 - Bouveault-Blanc Reduction
pp 76-78

21 - Bouveault Aldehyde Synthesis
pp 79-81

22 - Bucherer Reaction
pp 82-85

23 - Cannizzaro Reaction
pp 86-91

24 - Chapman Rearrangement
pp 92-94

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Name Reactions in Organic Synthesis

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