A ring expansion reaction of 1,3-oxathiolanes

descriptionPublicationkeyboard_double_arrow_right Article 24 Jan 2002Publisher:Royal Society of Chemistry (RSC)Journal:Chemical Communications (issn: 1359-7345, eissn: 1364-548X,

Copyright policy )

Authors: Maria, Ioannou; Michael J, Porter; Fabienne, Saez;

doi: 10.1039/b110754b

pmid: 12120067

A ring expansion reaction of 1,3-oxathiolanes

- Summary
- Subjects
- Metrics

Abstract

1,3-Oxathiolanes are efficiently converted, via sulfur ylide intermediates, to 1,4-oxathianes by ring expansion with a silylated diazoacetate in the presence of a copper catalyst.

Related Organizations

University College London
United Kingdom

Keywords

Organophosphorus Compounds, Dicarboxylic Acids, Indicators and Reagents, DNA-Directed RNA Polymerases, Sulfhydryl Compounds, Enzyme Inhibitors, Catalysis, Copper

Impact byBIP!

	selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	34
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Top 10%
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 10%