| Propargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis. | |
| | |
MedLine Citation:
|
PMID: 23340491 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
|
This article presents recent progress in the conversion of propargyl vinyl ethers into heterocyclic scaffolds and how this goal can be reached in a diversity-oriented approach. The article also includes examples of transformations of propargyl vinyl ethers where the propargyl vinyl ether moieties are formed in situ. Furthermore, related reactions transforming propargyl vinyl amines to heterocycles are discussed. |
| | |
Authors:
|
Zhi-Bin Zhu; Stefan F Kirsch |
Publication Detail:
|
Type: JOURNAL ARTICLE Date: 2013-1-23 |
Journal Detail:
|
Title: Chemical communications (Cambridge, England) Volume: - ISSN: 1364-548X ISO Abbreviation: Chem. Commun. (Camb.) Publication Date: 2013 Jan |
Date Detail:
|
Created Date: 2013-1-23 Completed Date: - Revised Date: - |
Medline Journal Info:
|
Nlm Unique ID: 9610838 Medline TA: Chem Commun (Camb) Country: - |
Other Details:
|
Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
|
Organic Chemistry, Bergische Universität Wuppertal, Gaussstr. 20, 42119 Wuppertal, Germany. sfkirsch@uni-wuppertal.de. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
|
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Conformational equilibria in carboxylic acid bimolecules: a rotational study of acrylic acid-formic ...
Next Document: Effect of dietary intervention to reduce the n-6/n-3 fatty acid ratio on maternal and fetal fatty ac...