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University of Illinois at Urbana-Champaign

An Anionic 3 + 2 Cyclization-Elimination Route to Cyclopentenes

Abstract

dc:description

Recently there has been considerable interest in the synthesis of five-membered carbocycles. In this thesis we discuss our work on the development and use of 1-benzenesulfonyl-2-carbamoylallyllithium reagents in an anionic 3+2 cyclization-elimination route to cyclopentenes.

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
  • Burg, Douglas Alan
Contributors dc:contributor
  • Beak, Peter

Subjects

dc:subject × 1

Identifiers

dc:identifier.*
Identifier
(UMI)AAI8908633
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/70419

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Burg, Douglas Alan. An Anionic 3 + 2 Cyclization-Elimination Route to Cyclopentenes. Dissertation thesis, University of Illinois at Urbana-Champaign, 2014. http://hdl.handle.net/2142/70419