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As many as six tandem reactions in one step! Unprecedented formation of highly functionalized benzothiophenesOpen AccessPublished in
2009
DOI: 10.1039/b914424b
PMID: 19921006
Issue: 46
Pages: 7131 - 7133
A novel reaction pathway involving 1,3-diketones and 2,2′- dithiodibenzoylchloride that gives access to benzothiophenes with spiroketal, lactone, carbonyl, hydroxyl and carboxylic acid functionalities is discussed. © The Royal Society of Chemistry 2009.
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Related Papers (3)
About the journal
| Journal | Chemical Communications |
|---|---|
| ISSN | 13597345 |
| Open Access | Yes |
Authors (1)
Kannoth Manheri Muraleedharan- 1-Hydroxymethyl-7-oxabicyclo[2.2.1]hept-2-ene skeleton in enantiopure form through enzymatic kinetic resolution
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Concepts (21)
Benzothiophene- Carbonyl derivative
- Carboxylic acid
- Chloride
- Ketone derivative
- Lactone
- Natural product
- Acylation
- Article
- Chemical reaction
- Isomer
- Methodology
- Oxidation
- Proton nuclear magnetic resonance
- Carboxylic acids
- Furans
- Ketones
- Lactones
- Methods
- Spiro compounds
- Thiophenes
