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University of Washington

Myers-Inspired Selenium-Mediated Isomerization: An Efficient Generation of Contra-Thermodynamic Allenes and Alkenes with the Potential for Reductive Deamination of Primary Amines and Metal-Free Hydrogenation of Dienes

Abstract

dc:description.abstract

Novel methods of catalytic metal-free isomerization reactions are scarce. By combining precedents in reductive defunctionalization reactions, coupled with previous advances in selenium-catalyzed C-N bond forming reactions, we have developed a contemporary but efficient manner of reaching contra-thermodynamic isomers of alkenes and alkynes. These isomerizations follow a well envisioned mechanistic path that may lead to further development in reductive deamination reactions, such as the reduction of primary amines such as anilines, and diamines to monoenes.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Landing, Samuel Dane
Advisor dc:contributor.advisor
  • Michael, Forrest E

Subjects

dc:subject × 6

Rights

dc:rights
Statement dc:rights
  • none
Language dc:language.iso
en_US

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1773/50734
OAI identifier oai:identifier
oai:digital.lib.washington.edu:1773/50734

Chain of custody

source
Harvested from
University of Washington
Base URL
digital.lib.washington.edu/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Landing, Samuel Dane. Myers-Inspired Selenium-Mediated Isomerization: An Efficient Generation of Contra-Thermodynamic Allenes and Alkenes with the Potential for Reductive Deamination of Primary Amines and Metal-Free Hydrogenation of Dienes. 2023. http://hdl.handle.net/1773/50734