Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Help & Advice
University of Warwick

The Library

  • Login
  • Admin

Bilirubin and its esters

Tools
- Tools
+ Tools

Johnson, Brian (1973) Bilirubin and its esters. PhD thesis, University of Warwick.

[img]
Preview
PDF
WRAP_Thesis_Johnson_1973.pdf - Requires a PDF viewer.

Download (6Mb) | Preview
Official URL: http://webcat.warwick.ac.uk/record=b1746210~S1

Request Changes to record.

Abstract

In this thesis some chemical aspects of the bile pigment bilirubin have been examined.

Bilirubin has been shown to exist as the bislactam tautomer, with an intranolocularly hydrogen bonded structure which is independent of the medium. Possible structures are discussed in Chapter 2.

The clinical determination of bilirubin involves treatment of the pigment with diazotised sulphanilic acid (the van den Bergh reaction) when bilirubin is cleaved at the central methylene bridge to form two azopigments. The fate of the central methylene bridge carbon atom was unknown until the present work, but it had been postulated as being liberated as formaldehyde. In Chapter 3, it is shown that formaldehyde is formed during this reaction, and that it can be detected by the product of its reaction with dimedone.

Some metal complexes of bilirubin formed in dipolar aprotic solvents are discussed in Chapter 4. A possible structure for the complex with Zn(II), isolated from DMF solution, is suggested.

In Chapter 5, a potentially extremely useful method for the synthesis of bilirubin conjugates of defined structures is examined, using substituted aryl triazenes, under mild conditions. This method allows the esterification of a specific hydroxyl group in a polyhydroxylated mono – or oligosaccaride without protection of the other hydroxyl group present. Thus, in this work, using l – alkyl -3-p- tolyltriazenes, the hitherto unknown diethyl, diisopropyl and dibenzyl esters of bilirubin have been prepared and characterised.

Item Type: Thesis (PhD)
Subjects: Q Science > QD Chemistry
Library of Congress Subject Headings (LCSH): Bilirubin, Bilirubin -- Metabolism, Esters
Official Date: 1973
Dates:
DateEvent
1973Submitted
Institution: University of Warwick
Theses Department: Department of Chemistry
Thesis Type: PhD
Publication Status: Unpublished
Supervisor(s)/Advisor: Hutchinson, D. W.(David Wesley) , Knell, A.J.
Sponsors: Medical Research Council (Great Britain)
Extent: 87, [16] leaves : illustrations
Language: eng

Request changes or add full text files to a record

Repository staff actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics

twitter

Email us: wrap@warwick.ac.uk
Contact Details
About Us