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University of Illinois at Urbana-Champaign
Studies on the 1-Aza-1 Prime -Oxa-(3,3)-Sigmatropic Rearrangement: Synthesis of Ortho-(beta-Oxoalkyl) Anilides and Regiospecifically Substituted Indoles
Abstract
dc:descriptionAlternate O-vinylating agents have also been investigated. The reactions of N-arylhydroxamic acids and (alpha)-chloroenamines gave rise to substituted anilides bearing a carboxamidomethyl substituent resulting from the O-vinylation of the hydroxamic acid and {3,3}-sigmatropic rearrangement.
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
-
- Burgoyne, William Franklin, Jr.
Subjects
dc:subject × 1Rights
- Language dc:language
- eng
Identifiers
dc:identifier.*- Identifier
- (UMI)AAI8114395
- OAI identifier oai:identifier
- oai:www.ideals.illinois.edu:2142/67256