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A Convenient Preparation of 3-Substituted Furans: Synthesis of Perillene and Dendrolasin
- Source :
- Organic Letters. 4:1387-1389
- Publication Year :
- 2002
- Publisher :
- American Chemical Society (ACS), 2002.
-
Abstract
- A variety of 3-substituted furans, including the natural products perillene and dendrolasin, are obtained in good yield via reductive annulation of 1,1,1-trichloroethyl propargyl ethers using catalytic Cr(II) regenerated by Mn/TMSCl. [reaction: see text]
- Subjects :
- Annulation
Alkylation
Acyclic Monoterpenes
Organic Chemistry
General Medicine
Biochemistry
Catalysis
Terpene
chemistry.chemical_compound
Perillene
Chlorides
chemistry
Chromium Compounds
Yield (chemistry)
Propargyl
Monoterpenes
Organic chemistry
Indicators and Reagents
Dendrolasin
Physical and Theoretical Chemistry
Furans
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....0a04a1780d7b1726aa912e3eef5d1e01
- Full Text :
- https://doi.org/10.1021/ol025708s