Repository logo
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo

LBCL Repository

  • Communities & Collections
  • All of DSpace
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Naik, Sarala"

Now showing 1 - 1 of 1
Results Per Page
Sort Options
  • No Thumbnail Available
    Item
    Tetrabutylammonium tribromide in organic synthesis & N-Acylation in aqueous medium
    (2006) Naik, Sarala
    The contents of this thesis have been divided into two chapters summarising the results based on the experimental works performed during the complete course of the research. Each chapter constitutes four sections, sections A-D describing introduction, present work, experimental work and spectral data respectively. Tetrabutylammonium tribromide (TBATB) in organic synthesis is the theme of chapter 1 in which various synthetically useful organic functional group transformations such as thioacetalisation, transthioacetalisation of carbonyl compounds, tetrahydropyranylation and depyranlation, acylation of alcohols and direct condensation of carboxylic acids with alcohols achieved utilising the in situ acidity of TBATB has been described. With the endeavour to understand the chemoselectivity in thioacetalisation, a brief theoretical study has been performed and described in chapter 1. The second chapter of this dissertation elucidates the results pertaining to N-acylation of amines in water serving as the reaction medium.
LBCL Digital Repository copyright © 2015-2023