Back to results
University of Illinois at Urbana-Champaign
(-)-Sparteine Mediated Lithiation of N-Boc-N-P-(methoxyphenyl) Allylic Amines and Conjugate Addition to Nitroalkenes: Scope, Reaction Pathway, and Synthetic Applications
Abstract
dc:descriptionThe enecarbamate products of the conjugate additions may also be easily elaborated to enantioenriched functionalized cyclopentanoids. Hydrolysis of the enecarbamates followed by intramolecular nitro-aldol cyclization and dehydration provides substituted nitrocyclopentenes that were converted to substituted cyclopentanones and cyclopentylamines.
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
- 2015
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Johnson, Timothy Allen
- Contributors dc:contributor
-
- Beak, Peter
Subjects
dc:subject × 1Rights
- Language dc:language
- eng
Identifiers
dc:identifier.*- Identifier
- (MiAaPQ)AAI3070342
- OAI identifier oai:identifier
- oai:www.ideals.illinois.edu:2142/84080