Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/67001
Title: Studies on the bridgehead and bridged hetero annulenes
Researcher: Sarma, Chandra Sekhar
Guide(s): Kataky, J C S
Keywords: Acylation
Annulenes
Catalyst
Cycloaddition
Dipolar
Haloform
Hetero
Phosphorus
University: Gauhati University
Completed Date: 31/12/1991
Abstract: Annulene chemistry, one of the most important parts of Organic chemistry both from theoretical and practical point of view, play a key role in the studies of aromaticity in various bridged and heterobridge orga-nic compounds. The synthesis of 1,6-methano[10]annulene and their mono and disubstituted derivatives by using newer reagents comprise the subject of the present thesis. At the same time attempt has been made to study the addition and cycloaddition reactions of 1,3,5-cyclohepta-1,6-dicarboxa-mide with carbondisulphide and various derivatives of dichlorophosphoro-chloridate and thiophosphorochlorioate respectively. The results of these investigation are presented in six chapters comprising the Part-I. A brief introductory note is also given at the beginning of these chapters. In Part-II, the cycloaddition reactions of substituted hydrazones has been discussed. In the introductory note a brief review of the historical develop-ment and published literature on [10],[12],[14],[16],[18],[20] and [22]annulene system are given. PART - I CHAPTER ONE SYNTHESIS OF THE KEY INTERMEDIATE (Scheme 1) 1.1 Synthesis of monoacetyl cyclohepta-1,3,5-triene (II) : This chapter commence with the synthesis of monoacetyl cyclohepta 1,3,5-triene from the starting material cyclohepta-1,3,5-triene (I) using weak Lewis acid (ZnCl2) as catalyst for the Friedel-Crafts acylation reaction. 1.2 Synthesis of 1,6-diacetyl cyclohepta-1,3,5-triene (III) : This diacetylated liquid compound (III) was prepared by the same F. C. reaction under controlled condition using strong Lewis acid (AlCl3) as catalyst and the monoacetyl derivative (II) as the starting material. 1.3 Synthesis of cyclohepta-1,3,5-triene-1,6-dicarboxylic acid (IV) : The diacetyl cyclohepta-1,3,5-triene (III) upon haloform reaction under controlled condition, yielded the solid title dicarboxylic acid (IV). 1.4 Synthesis of cyclohepta-1,3,5-triene-1,6-diacid dichloride (V) : The title compound (V) was prepared from the above dicarboxylic acid (IV) by simple chlorination of the...
Pagination: 
URI: http://hdl.handle.net/10603/67001
Appears in Departments:Department of Chemistry

Files in This Item:
File Description SizeFormat 
01_title page.pdfAttached File19.71 kBAdobe PDFView/Open
02_dedicated.pdf3.43 kBAdobe PDFView/Open
03_certificate.pdf50.14 kBAdobe PDFView/Open
04_content.pdf22.02 kBAdobe PDFView/Open
05_preface.pdf17.65 kBAdobe PDFView/Open
06_acknowledgement.pdf41.97 kBAdobe PDFView/Open
07_general remarks.pdf19.83 kBAdobe PDFView/Open
08_abbreviations used.pdf10.93 kBAdobe PDFView/Open
09_abstract.pdf274.54 kBAdobe PDFView/Open
10_chapter 1.pdf1.07 MBAdobe PDFView/Open
11_chapter 2.pdf494.47 kBAdobe PDFView/Open
12_chapter 3.pdf686.98 kBAdobe PDFView/Open
13_chapter 4.pdf633.79 kBAdobe PDFView/Open
14_chapter 5.pdf519.83 kBAdobe PDFView/Open
15_chapter 6.pdf316.94 kBAdobe PDFView/Open
16_chapter 7.pdf289.46 kBAdobe PDFView/Open
17_chapter 8.pdf308.26 kBAdobe PDFView/Open


Items in Shodhganga are protected by copyright, with all rights reserved, unless otherwise indicated.