Synthesis of benzofurans from oxygenated phenoxyamines
Journal Article
·
· J. Org. Chem.; (United States)
O-Aryloximes having various oxygenated substitution patterns have been converted to benzofurans, with implications toward natural product synthesis, through an extension of the Fischer indole type of synthesis. The effect of the substituent pattern in the benzene ring and the nature of the carbonyl derived portion of the oxime on benzofuranization were explored. 11 references, 4 tables.
- Research Organization:
- Univ. of California, Berkeley
- DOE Contract Number:
- AC03-76SF00098
- OSTI ID:
- 6060646
- Journal Information:
- J. Org. Chem.; (United States), Journal Name: J. Org. Chem.; (United States) Vol. 49:23; ISSN JOCEA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400301* -- Organic Chemistry-- Chemical & Physicochemical Properties-- (-1987)
AMINES
AROMATICS
BENZOFURANS
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
DATA
EXPERIMENTAL DATA
FURANS
HETEROCYCLIC COMPOUNDS
HYDROXY COMPOUNDS
INFORMATION
KETONES
NMR SPECTRA
NUMERICAL DATA
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXIMES
SPECTRA
STRUCTURAL CHEMICAL ANALYSIS
SYNTHESIS
ULTRAVIOLET SPECTRA
YIELDS
400301* -- Organic Chemistry-- Chemical & Physicochemical Properties-- (-1987)
AMINES
AROMATICS
BENZOFURANS
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
DATA
EXPERIMENTAL DATA
FURANS
HETEROCYCLIC COMPOUNDS
HYDROXY COMPOUNDS
INFORMATION
KETONES
NMR SPECTRA
NUMERICAL DATA
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXIMES
SPECTRA
STRUCTURAL CHEMICAL ANALYSIS
SYNTHESIS
ULTRAVIOLET SPECTRA
YIELDS