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University of Illinois at Urbana-Champaign

Extension of Chromatographically - Derived Molecular Recognition Concepts to Stereoselective Reactions and Transformations

Abstract

dc:description

Analogues of chiral stationary phases (CSPs) and analogues of enantiomeric analytes separable upon the CSPs were employed in the investigation of stereoselective reactions and transformations. N-(3,5-dinitrobenzoyl)phenylglycine and N-(3,5-dinitrobenzoyl)leucine were used to study the stereochemical course of the coupling of chiral acids and chiral amines.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Reno, Daniel Scott

Subjects

dc:subject × 1

Identifiers

dc:identifier.*
Identifier
(UMI)AAI8803175
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/70394

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Reno, Daniel Scott. Extension of Chromatographically - Derived Molecular Recognition Concepts to Stereoselective Reactions and Transformations. Dissertation thesis, University of Illinois at Urbana-Champaign, 2014. http://hdl.handle.net/2142/70394