Document Detail


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.
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