https://search.dev.ndltd.org/etd/creighton/oai:cdr.creighton.edu:10504/107625
type: CreativeWork
name: 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.
description: 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.
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.
author: Pirruocello, Sebastian Charles
language: en_US
date published: 1952
date modified: 2026-07-24T01:50:46Z
provider: Creighton University
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: Creighton University

PropertyValue
property ID: Handle
value: http://hdl.handle.net/10504/107625