Abstract
dc:description.abstractFor many years, acrylonitrile has afforded the organic chemist a convenient method of introducing a three-carbon residue onto a variety of organic compounds by the so-called cyano-ethylation reaction. This reaction is generally brought about by a base-catalyzed, nucleophilic addition. The purpose of this work is to investigate and to evaluate the applicability of the readily-available diethyl 2,4-dicyanoglutaconate in a similar type of reaction. Such a reaction, if feasible, would permit the introduction of a seven-carbon residue which possesses reactive terminal functional groups. This would be of great value in synthetic organic chemistry.
Degree
thesis:*- Grantor dc:publisher
- Creighton University
- Year dc:date.issued
- 1962
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Di Mari, Samuel J.
- Advisor dc:contributor.advisor
-
- Takemura, Kaz H.
Rights
dc:rights- Statement dc:rights
-
- A non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above.
- Language dc:language.iso
- en_US
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/10504/109028
- OAI identifier oai:identifier
- oai:cdr.creighton.edu:10504/109028