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Synthesis of benzofurans from oxygenated phenoxyamines

Journal Article · · J. Org. Chem.; (United States)
DOI:https://doi.org/10.1021/jo00197a014· OSTI ID:6060646

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