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University of Saskatchewan

ALDOL COUPLINGS OF CHIRAL FRAGMENTS WITH KINETIC RESOLUTION: SCOPE AND LIMITATIONS

Abstract

dc:description.abstract

“The Thiopyran Route to Polypropionates” is a synthetic strategy that involves the stepwise aldol reactions of 6 and 7a to rapidly access stereochemically complex tetrapropionate 8 and hexapropionate synthons 72 or 73. Coupling racemic 7a with any of the four enantioenriched diastereomers 8 with kinetic resolution (KR) is possible with rational design of the reaction using the 'multiplicativity' rule. Thus, any of two of the eight possible aldol adducts, 72 or 73, are selectively available from the same reactants.

Degree

thesis:*
Name thesis:degree_name
Master of Science (M.Sc.)
Level thesis:degree_level
Masters
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Saskatchewan
Year dc:date.issued
2013

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • kazemeini, alieh
Advisor dc:contributor.advisor
  • Ward, Dale
Committee members dc:contributor.committeemember
  • Majewski, Marek
  • Gravel, Michel
  • Attah-Poku, Samuel

Subjects

dc:subject × 1

Rights

Language dc:language.iso
eng

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:harvest.usask.ca:10388/ETD-2011-12-244

Chain of custody

source
Harvested from
University of Saskatchewan
Base URL
harvest.usask.ca/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

kazemeini, alieh. ALDOL COUPLINGS OF CHIRAL FRAGMENTS WITH KINETIC RESOLUTION: SCOPE AND LIMITATIONS. Masters thesis, University of Saskatchewan, 2013. https://hdl.handle.net/10388/ETD-2011-12-244