Ding, Xiaoyuan
(2006)
Synthesis of Quasienantiomeric Fluorous-Tagged Oxazolidinonesand Application in Alkylation and syn-Aldol Reactions.
Master's Thesis, University of Pittsburgh.
(Unpublished)
Abstract
Evans' oxazolidinones are among the most well-established and extensively used chiral auxiliaries for stoichiometric asymmetric methods in total synthesis. The most common applications are á-alkylation and syn-aldol reactions, which build either enantiomers or diastereomers containing flexible function groups for further elaboration. Fluorous quasiracemic synthesis involves synthesis of both enantiomers of a target compound in a single synthesis by implementation of a fluorous tagging strategy. Here, two different fluorous-tagged oxazolidinones were synthesized in an efficientt synthetic strategy. Preliminary alkylation and aldol condensation of the fluorous-tagged imides derived from the corresponding oxazolidinones were carried out and compared with the non fluorous-tagged imide in the aspect of yield and diastereomer ratios. The alkylation and aldol reactions of the quasiracemic mixture were conducted and the resultant crude products were subjected to HPLC analysis.
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Details
Item Type: |
University of Pittsburgh ETD
|
Status: |
Unpublished |
Creators/Authors: |
|
ETD Committee: |
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Date: |
29 June 2006 |
Date Type: |
Completion |
Defense Date: |
29 January 2006 |
Approval Date: |
29 June 2006 |
Submission Date: |
28 April 2006 |
Access Restriction: |
No restriction; Release the ETD for access worldwide immediately. |
Institution: |
University of Pittsburgh |
Schools and Programs: |
Dietrich School of Arts and Sciences > Chemistry |
Degree: |
MS - Master of Science |
Thesis Type: |
Master's Thesis |
Refereed: |
Yes |
Uncontrolled Keywords: |
oxazolidinones |
Other ID: |
http://etd.library.pitt.edu/ETD/available/etd-04282006-130951/, etd-04282006-130951 |
Date Deposited: |
10 Nov 2011 19:42 |
Last Modified: |
15 Nov 2016 13:42 |
URI: |
http://d-scholarship.pitt.edu/id/eprint/7709 |
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