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Creighton University

The Preparation of: 1. 1-(p-Methoxyphenyl)-2,6-dicarbethoxy-5-amino-cyclohexenone-3. 2. 1-(p-Methoxyphenyl)-2,6-dicarbethoxy-4-cinnamoyl-cyclohexane-dione-3,5. 3. diidodo derivative of 1-(p-Hydroxyphenyl)-2,6-dicarbethoxy-cyclohexane-dione-3,5.

Abstract

dc:description.abstract

For this type of reaction to tabs place, the methylene group requires the activating influence of an adjacent CC, -CN, or -NO2 grouping. A heterocyclic, or an aromatic group, or a conjugated system have the same effect.

Degree

thesis:*
Grantor dc:publisher
Creighton University
Year dc:date.issued
1952

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Pirruocello, Sebastian Charles
Advisor dc:contributor.advisor
  • Papadakis, Phillippos E.

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/10504/107625
OAI identifier oai:identifier
oai:cdr.creighton.edu:10504/107625

Chain of custody

source
Harvested from
Creighton University
Base URL
cdr.creighton.edu/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Pirruocello, Sebastian Charles. The Preparation of: 1. 1-(p-Methoxyphenyl)-2,6-dicarbethoxy-5-amino-cyclohexenone-3. 2. 1-(p-Methoxyphenyl)-2,6-dicarbethoxy-4-cinnamoyl-cyclohexane-dione-3,5. 3. diidodo derivative of 1-(p-Hydroxyphenyl)-2,6-dicarbethoxy-cyclohexane-dione-3,5.. Creighton University, 1952. http://hdl.handle.net/10504/107625