Repository logo
Log In(current)
  1. Home
  2. Colleges & Schools
  3. Graduate School
  4. Doctoral Dissertations
  5. Rearrangements of the Benzilic Acid Type; Preparation and Use of Dialkali Metal Adducts of Aromatic Ketones.
Details

Rearrangements of the Benzilic Acid Type; Preparation and Use of Dialkali Metal Adducts of Aromatic Ketones.

Date Issued
August 1, 1959
Author(s)
Selman, Stanley
Advisor(s)
Jerome F. Eastham
Additional Advisor(s)
D. A. Shirley
Carl Buehler
John W. Prados
Permanent URI
https://trace.tennessee.edu/handle/20.500.14382/24036
Abstract

Introduction: The benzilic acid rearrangement is the base-catalyzed transformation of an α-diketone to the salt of an α-hydroxy acid. This rearrangement can be effected in aromatic, semi-aromatic (o-quinones), in alicyclic, and aliphatic, as well as in heterocyclic α-diketones. Examples of the rearrangement in the above type compounds are illustrated in equations 1-6.

Disciplines
Chemistry
Degree
Doctor of Philosophy
Major
Chemistry
Embargo Date
August 1, 1959
File(s)
Thumbnail Image
Name

SelmanStanley_1959_OCRed.pdf

Size

5.17 MB

Format

Adobe PDF

Checksum (MD5)

fe626d6e5ebdd4df09684e9b71994fb5


University Libraries

1015 Volunteer Boulevard
Knoxville, TN 37996
865-974-4351

Map & Directions
Donate to the Libraries
  • About
  • John C. Hodges Society
  • Speaking Volumes magazine
  • Outreach
  • Directory
  • Employment
  • Policies
  • Library Intranet
University of Tennessee power T logo

The University of Tennessee, Knoxville
Knoxville, Tennessee 37996
865-974-1000

Events
A-Z
Apply
Privacy
Map
Directory
Give to UT
Accessibility

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science