dc.contributor.author |
Mohamed S. Sasi |
|
dc.contributor.author |
Abdulfattah M. Alkherraz |
|
dc.contributor.author |
Mohamed A. Elsirkasi |
|
dc.date.accessioned |
2024-11-28T08:02:53Z |
|
dc.date.available |
2024-11-28T08:02:53Z |
|
dc.date.issued |
2014-12-01 |
|
dc.identifier.issn |
2518-5454 |
|
dc.identifier.uri |
http://dspace-su.server.ly:8080/xmlui/handle/123456789/1524 |
|
dc.description.abstract |
The research project aim is to determine the pKa of neopentanol alcohol because it has been used in many biological models as a leaving group. The pKa of neopentanol alcohol can be obtained by measuring the observed rate for compound 1 under identical conditions to that reported for a similar series of alkyl uridyl phosphate diesters. The pKa of neopentyl alcohol was derived from the reported Brønsted plot for the hydroxide-catalyzed hydrolysis of alkyl uridyl phosphate diesters and the observed rate constant for uridine 3´-neopentyl phosphate 1. As a result, the best estimate for the pKa of neopentanol alcohol can established from this work. The corresponding pKa of neopentyl alcohol from the observed rate of the hydroxide-catalyzed hydrolysis of 1 is 17.3, which is significantly greater than the value of 15.5 used in earlier reports. This new value can be used now to estimate a better half- life for pH-independent DNA cleavage. This allows us to use correctly the neopentyl group as a mimicked model for biological systems such as that in DNA cleavage |
en_US |
dc.language.iso |
other |
en_US |
dc.publisher |
جامعة سرت - Sirte University |
en_US |
dc.relation.ispartofseries |
المجلد الرابع - العدد الثاني - ديسمبر 2014;48-57 |
|
dc.subject |
Phosphate and Acetate Hydrolysis |
en_US |
dc.subject |
Neopentanol |
en_US |
dc.title |
The Hydrolysis of Alkyl-3'Uridyl Phosphate or Acetate Esters Can be Used to Estimate the pKa of Neopentyl Alcohol |
en_US |
dc.type |
Article |
en_US |